Arginase Bladder™

Product #160

Arginase Bladder™

Arginase Bladder is a 100% Food supplement that is intended to supply nutrients to support healthy kidney and bladder function. The kidneys process proteins and liquids and are the primary organs involved in eliminating metabolic waste products from the blood. 

90 Capsules   •   $33.00

Gluten-Free

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Product Details

Arginase Bladder contains ingredients which have been used to nutritionally support the bladder and various aspects of urine metabolism. It is intended to support the cleansing ability of the kidneys.

“The liver has the greatest amount of this enzyme, and accounts for the majority of urea synthesis”[a] small amount is carried out by the kidney and brain” the hydrolysis of arginine to urea and ornithine makes possible the urea cycle” [1]. An excess accumulation of arginine (due to insufficient arginase) contributes to excessively frequent urination (as the body tries to flush this diluted semi-urine out) and increases in urinary tract infections (as this less concentrated semi-urine is a less hostile environment for pathogens than concentrated urine is). “The liver is well known for its ability to detoxify or excrete many drugs, hormones, and other substances” [2]. The liver tissue found in Arginase Bladder is from New Zealand.

References
[1] Bondy PK, Rosenberg LE. Duncan”s Diseases of Metabolism, 7th ed. W.B. Saunders Co., Phil., 1974
[2] Guyton AC, Hall JE. Textbook of Medical Physiology, 9th ed. WB Saunders, Phil., 1996

Other ingredients: Vegetarian Capsule.
Suggested use: Serving size or as recommended by your health care professional. Adjust usage according to nutritional lifestyle requirements.

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

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Call Us at (805) 489-7185 or Email Us at doctorsfoodresearch@gmail.com for more info.

This site provides information for doctors and health care professionals and is not intended for use by consumer. 

Photos and Images are all used by permission from Pixabay.com & Pexels.com except for those that are Owned and Copyrighted by Doctors’ Research, Inc.

Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

Aller-Lung Support™

Product #135

Aller-Lung Support™

Aller-Lung Support™ is a 100% vegan Food supplement that intended to supply nutrients needed to maintain and support optimal sinus, lung, and immune system health.

90 Capsules   •   $32.00

Vegetarian Formula

Gluten-Free

Pareve Certified

Halal Certified

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Product Details

The immune system is quite complex, but when it reacts to normally harmless foods and pollen allergies, sinus complaints can result.  Aller-Lung Support™ is intended to supply nutrients to the sinuses, lungs and bronchial system.  

The 100% Food Aller-Lung Support™  formula contains herbs that can help support the lungs and sinuses.  For people with year-round or seasonal allergies, naturally-inclined doctors advise Food Aller-Lung Support™ .

Unlike many so-called “natural” formulas, Aller-Lung Support™ is only comprised of foods, no synthetic USP nutrients or isolated mineral salts, but only contains foods, food complexes, and food concentrates.  Studies indicate that food nutrients ARE better than isolated USP nutrients and MAY BE better absorbed retained, and utilized than USP nutrients.

Other ingredients:  Vegetarian Capsule.
Suggested use: Serving size or as recommended by your health care professional. Adjust usage according to nutritional lifestyle requirements.

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

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Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

Vitamin-Mineral™

Product #814 (SM) / #815 (LG)

Vitamin-Mineral™

Vitamin-Mineral™ is a 100% vegetarian Food supplement that is the best multi-vitamin, multi-mineral product available anywhere.

90 Tablets (SM)   •   $40.00
270 Tablets (LG)   •   $112.00

Vegetarian Formula

Gluten-Free

Pareve Certified

Halal Certified

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Product Details

Food  Vitamins and Minerals ARE Better!

Most multi-vitamin formulas are primarily synthetic (e.g. petroleum-derived) vitamins plus crushed industrial rocks, yet even peer reviewed medical research has concluded that food vitamins are superior to synthetics [1].

Numerous scientific papers have concluded that Food vitamins and minerals are better than USP isolated ‘nutrients’ because they contain important enzymes, peptides and phytonutrients which are critical to the utilization of vitamins and minerals and are lacking in isolated USP nutrients [e.g. 1,2].

All nutrients are contained in the following foods: Acerola Cherry, Alfalfa, Brown Rice, Carrots, Enzymatically processed Saccharomyces Cerevisiae, and Mixed Citrus.
Other ingredients: Fatty Acid from Palm Kernel, Vegetarian Coating.
Suggested use: Serving size or as recommended by your health care professional. Adjust usage according to nutritional lifestyle requirements.

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

Disclaimer: This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

Online Store for Healthcare Professionals

Call Us at (805) 489-7185 or Email Us at doctorsfoodresearch@gmail.com for more info.

This site provides information for doctors and health care professionals and is not intended for use by consumer. 

Photos and Images are all used by permission from Pixabay.com & Pexels.com except for those that are Owned and Copyrighted by Doctors’ Research, Inc.

Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

Metabolic Thyro™

Product #570

Metabolic Thyro™

Metabolic Thyro™ is a 100% Food supplement that is intended to supply nutrients, glandulars, and herbs needed to maintain and support optimal thyroid health. It contains both naturally-iodine containing kelp, plant source l-tyrosine, bovine glandulars, and herbs to support an optimally functioning thyroid.

90 Tablets   •   $28.00

Gluten-Free

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Product Details

Metabolic Thyro™ naturally contains carbohydrates (including all known essential monosaccharides), essential lipids, and proteins (including all ten essential amino acids) as found in specially grown, enzymatically processed Saccharomyces Cerevisiae and the individually listed foods. All glandulars are New Zealand source.

Metabolic Thyro™ contains no synthetic USP nutrients or isolated mineral salts.

Other ingredients: Enzymatically processed Saccharomyces Cerevisiae, Fatty Acid from Palm Kernel, Plant Polysaccharides, Silica.
Suggested use: Serving size or as recommended by your health care professional. Adjust usage according to nutritional lifestyle requirements.

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

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This site provides information for doctors and health care professionals and is not intended for use by consumer. 

Photos and Images are all used by permission from Pixabay.com & Pexels.com except for those that are Owned and Copyrighted by Doctors’ Research, Inc.

Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

Gluco-Sugar-Balance™

Product #358

Gluco-Sugar-Balance™

Gluco-Sugar-Balance™ is a 100% vegan Food supplement that is intended to help support the healthy balance of glucose in the body.

90 Capsules   •   $37.00

Vegetarian Formula

Gluten-Free

Pareve Certified

Halal Certified

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Product Details

 Gluco-Sugar-Balance™ contains minerals, such as chromium GTF and vanadium, as well as herbs to nutritionally support the body’s blood sugar systems.

Unlike many so-called “natural” vitamin formulas, Gluco-Sugar-Balance™ is 100% Food, it does not contain any synthetic USP nutrients, it only contains wildcrafted foods, food complexes, and food concentrates. Wildcrafted foods are foods such as found wild in nature or otherwise grown without the use of pesticides, preservatives, or herbicides.

Gluco-Sugar-Balance™ contains naturally occurring potassium, polysaccharides, CoQ10, glutathione, lipoic acid, trace minerals, enzymes, peptides, RNA/DNA, carbohydrates, lipids, proteins (including all ten essential amino acids), protein chaperones, and the antioxidant superoxide dismutase as found in enzymatically processed Saccharomyces cerevisiae and the other listed foods.

This product has been tested free of pesticides, herbicides, gluten, dairy, and soy.

Food nutrients ARE better than isolated USP nutrients and MAY BE better absorbed, retained, and utilized than USP nutrients. Food nutrients are better because they contain important enzymes, peptides, and phytonutrients CRITICAL to the UTILIZATION of vitamins and minerals which are not in isolated USP nutrients (and the Nobel prize for medicine was once awarded for part of this discovery). MEDLINE published research has concluded that food vitamins and food minerals are SUPERIOR to synthetic ones.

Other ingredients: Enzymatically processed Saccharomyces Cerevisiae, Vegetarian (HPMC) Capsule.
Suggested use: Serving size or as recommended by your health care professional. Adjust usage according to nutritional lifestyle requirements.

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

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Call Us at (805) 489-7185 or Email Us at doctorsfoodresearch@gmail.com for more info.

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Herbal

This site provides information for doctors and health care professionals and is not intended for use by consumer. 

Photos and Images are all used by permission from Pixabay.com & Pexels.com except for those that are Owned and Copyrighted by Doctors’ Research, Inc.

Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

B Stress Complex™

Product #174

B Stress Complex™​

B Stress Complex™ is a 100% vegetarian Food supplement that is intended to supply 100% Food B vitamins. Unlike certain so called “whole food” B vitamin sources, it does not contain isolated USP niacinamide, pyridoxine hydrochloride, or any isolated “nutrients”. 

90 Capsules   •   $40.00

Vegetarian Formula

Gluten-Free

Pareve Certified

Halal Certified

Have questions? Call by tapping below

Product Details

B Vitamins and certain herbs have been shown to help reduce stress (e.g. B5-pantothenate is even known as the “anti-stress vitamin”) [1,2,3]. B vitamins (B1, B2, B3, B5, B6, B8-inositol, B9-folate, B12) are necessary for energy metabolism and inadequate amounts can lead to pernicious anemia, low hemoglobin counts, skin problems, nervous system problems, and even serious mental problems [1].  

B Stress Complex™ naturally contains carbohydrates, lipids, proteins (including all ten essential amino acids), and superoxide dismutase as found in specially grown, enzymatically processed Saccharomyces cerevisiae, and organic brown rice. 

Unlike many so-called “natural” formulas, B Stress Complex™ is only comprised of foods, no synthetic USP nutrients or isolated mineral salts, but only contains foods, food complexes, and food concentrates.

B Stress Complex™ is a true Food supplement for today’s stressful society. It is a very popular with vegetarians, as well as anyone interested in a non-synthetic B complex formula.  

Studies have shown that Food B Vitamins are between 38% and 294% better absorbed into the blood when compared with typical USP B Vitamins.  

Other ingredients: Enzymatically processed Saccharomyces Cerevisiae
Vegetarian Capsule.
Suggested use: Serving size or as recommended by your health care professional.
Adjust usage according to nutritional lifestyle requirements.

References
[1] Shils ME, Olson JA, Shike J. Modern Nutrition in Health and Disease, 8th ed. Lea and Febiger, Phil., 1994; 9th ed. Williams & Wilkins, Balt., 1999
[2] Understanding Vitamins and Minerals. Rodale Press, Emmaus (PA), 1984
[3] PDR for Herbal Medicine, 2nd ed. Medical Economics, Montvale (NJ), 2000

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

Online Store for Healthcare Professionals

Call Us at (805) 489-7185 or Email Us at doctorsfoodresearch@gmail.com for more info.

BEST SELLERS!

More Products

Vegetarian

Glandular

Herbal

This site provides information for doctors and health care professionals and is not intended for use by consumer. 

Photos and Images are all used by permission from Pixabay.com & Pexels.com except for those that are Owned and Copyrighted by Doctors’ Research, Inc.

Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

Cardio Power™

Product #230

Cardio-Power™

Cardio-Power™ is a 100% Food supplement that is intended to supply nutrients, glandulars, and herbs needed to maintain and support optimal cardiac muscle health. 

90 Capsules   •   $28.00

Gluten-Free

Have questions? Call by tapping below

Product Details

The heart pumps blood containing oxygen and other nutrients throughout the body. Bovine heart tissue naturally contains vital heart nutrients like co-enzyme Q10.

Cardio-Power™ provides nutritional support for the heart and for overall circulation. Current and historical references suggest that substances contained within the ingredients in Cardio-Power™ can nutritionally help support the heart, increase endurance, aid with energy, and promote better overall health. Some with cardiovascular concerns are often cold, have cold extremities (cold hands and feet), while others simply get exhausted too easily. 

The cardiovascular system is too important to rely on a few incomplete isolated nutrients, Cardio-Power™ is made up of the highest quality Foods to provide the nutrients that natural healthcare professionals are looking for to support the cardiovascular system.

Cardio-Power™ is also taken by athletes interested in better performance, individuals who want more energy, as well as by many with hypotension.

Other ingredients: Enzymatically processed Saccharomyces Cerevisiae, Organic Brown Rice, Vegetarian (HPMC) Capsule.
Suggested use: Serving size or as recommended by your health care professional. Adjust usage according to nutritional lifestyle requirements.

No Synthetic Nutrients&nbsp • &nbspNo Dairy&nbsp • &nbspNo Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

No Synthetic Nutrients • No Dairy • No Preservatives

* This is a nutritional product and not a medication intended to prevent, treat, or cure any illness. None of these statements has been approved by the US FDA or similar agencies. Not all citations meet peer-reviewed status so the statements are not conclusive. Professionals can, and do, disagree, regarding efficacy of ingredients in nutritional formulas.

Disclaimer: Some of these studies (or citations) may not confom to peer review standards. Therefore, the results are not conclusive. Profressionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA.

Online Store for Healthcare Professionals

Call Us at (805) 489-7185 or Email Us at doctorsfoodresearch@gmail.com for more info.

This site provides information for doctors and health care professionals and is not intended for use by consumer. 

Photos and Images are all used by permission from Pixabay.com & Pexels.com except for those that are Owned and Copyrighted by Doctors’ Research, Inc.

Copyright 2025 © All Rights Reserved. Developed and Designed by James Erwin Estoque

Food Antioxidants Are Superior To Isolated Antioxidants

Abstract: Although many people take isolated nutrients as antioxidant supplements, they may not be getting the benefits they hope for. While isolated nutrients have powerful antioxidant abilities in vitro, they rarely have significant antioxidant benefits in vivo. High antioxidant containing foods have proven benefit in humans (in vivo) and high antioxidant effects in vitro as well. High antioxidant containing plants and other herbs are recommended for those interested in obtaining true antioxidant benefits.

Introduction

We live in a world where free radicals can come from many sources and contribute to deterioration of health. “Sources of free radicals include pollutants, drugs, metal ions, radiation, high intakes of polyunsaturated fatty acids, strenuous exercise, mitochondrial dysfunction and smoking. These may result in damage to membrane lipids, proteins, nucleic acids and carbohydrates, which can result in cancer, neurological diseases, lung diseases, diabetes, vascular diseases, autoimmune diseases, aging and eye diseases” [1]. Each day, each cell in the human body endures 104 hits from free radicals—that is about three hundred trillion hits to the body per day!

Antioxidants can inhibit oxidation by giving away an oxygen molecule without requiring much energy. Oxidation is the addition of oxygen or the removal of hydrogen and can be caused by free radicals. An antioxidant can slow down or even stop the chain reaction of oxidation by giving away an electron without changing its stability. Many believe that since real antioxidants can prevent free radical damage, that perhaps aging and various chronic conditions can, to some degree, be slowed down through the consumption of isolated antioxidant nutrients. Is this belief correct?

It is true that free radical damage to the skin contributes greatly to the aged appearance of the skin [2]. It is true that the consumption of high antioxidant containing foods is associated with a decreased risk of cancer and cardiovascular disease [3]. It is true that the consumption of high amounts of antioxidant containing foods is correlated with reduced risk of Alzheimer’s [4]. “Epidemiological studies have shown that consumption of fruits and vegetables is associated with reduced risk of chronic diseases. Increased consumption of fruits and vegetables containing high levels of phytochemicals has been recommended to prevent chronic diseases related to oxidative stress in the human body” [5].

Yet, it is also true that every large clinical trial, which has used isolated antioxidant supplements, has failed to show benefit for cancer and cardiovascular disease [6,7]. It is also true that in a recent trial, “The intake of {ISOLATED} vitamin C, beta-carotene and vitamin E supplements was not significantly associated with the risk of Alzheimer’s disease” [8]. “In two recent observational studies, higher dietary intakes of antioxidants {FOOD}, especially {FOOD} vitamin E, were found to be associated with a lower risk of Alzheimer’s disease. Neither study showed that supplemental {ISOLATED} vitamin E and vitamin C reduced the risk of Alzheimer’s disease. These findings suggest the involvement of other nutritional factors that may be involved in the reduced risk” [9].

(Note: Any words in this paper contained within {} are supplied by this investigator for clarification.)

Food vs. Isolated Form Nutrients

It should be understood that some who have concluded that antioxidant vitamins have little positive effect in vivo have normally failed to realize that the chemical forms of antioxidants used in these trials are often not quite the same as the form found in food.

Food antioxidants, be they vitamins, minerals, or concentrated herbs are superior to the commonly sold non-foods (note only officially recognized vitamins/minerals are listed below):

Food NutrientCompared to USP Vitamin/Mineral Salt
BetacaroteneProvides much greater betacarotene diversity in blood [10]
Vitamin COver 15.6 times antioxidant effect [11]
Vitamin EUp to 4.0 times the free radical scavenging strength [12]
SeleniumNearly 2 times better retained [13]
ZincBetter absorption, better form [14,15]

Many have erroneously concluded that taking many times the quantity of isolated antioxidants will give the same effect as consuming food antioxidants. However, the differences are more than absorption or antioxidant effectiveness. Most isolated ‘antioxidant’ nutrients are chemically and structurally different from those found in foods and do not have the same effect in the human body.

Beta-carotene has been found to have antioxidant effect in vitro…Whether {ISOLATED} beta-carotene has significant antioxidant effect in vivo is unclear” [16]. Carrots, a food high in betacarotene, do have high antioxidant ability [5,16]. Natural betacarotene, as found in foods, is composed of both all-trans and 9-cis isomers, while synthetic betacarotene is all-trans isomers [17]. Carrots, yellow and green leafy vegetables, and turmeric contain natural betacarotene along with multiple carotenoids. Natural betacarotene was found to significantly decrease serum conjugated diene levels for children exposed to high levels of irradiation, though it is not known if synthetic betacarotene would provide similar benefits [17].

Regarding isolated betacarotene, “The data presented provide convincing evidence of the harmful properties of this compound if given alone to smokers, or to individuals exposed to environmental carcinogens, as a micronutrient supplement” [7]. “The three beta-carotene intervention trials: the Beta Carotene and Retinol Efficacy Trial (CARET), Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study (ATBC), and Physician’s Health Study (PHS) have all pointed to a lack of effect of synthetic beta-carotene in decreasing cardiovascular disease or cancer risk in well-nourished populations. The potential contribution of beta-carotene supplementation to increased risk of lung cancer in smokers has been raised as a significant concern. The safety of synthetic beta-carotene supplements and the role of isomeric forms of beta-carotene (synthetic all-trans versus “natural” cis-trans isomeric mixtures)… have become topics of debate in the scientific and medical communities” [18]. Now, although the consumption of both synthetic betacarotene and food betacarotene raise serum vitamin A levels about the same, this obscures the fact that synthetic betacarotene tends to mainly increase serums all-trans betacarotene, while food betacarotene increases other forms as well [19].

It is possible that synthetic betacarotene can negatively affect vitamin E’s antioxidant ability as a clinical study found, “These results support earlier findings for the protective effect of a-tocopherol against LDL oxidation, and suggest that beta-carotene participates as a prooxidant in the oxidative degradation of LDL under these conditions. Since high levels of alpha-tocopherol did not mitigate the prooxidative effect of beta-carotene, these result indicate that increased LDL beta-carotene may cancel the protective qualities of alpha-tocopherol” [20]. In a consumer-directed publication, Stephen Sinatra (M.D.) observes, “Research has shown that high doses of synthetic beta-carotene—the kind found in many popular brands—may actually increase your risk for lung cancer. Because at high levels it can become prooxidative—exactly the opposite of what you want…I’ve seen harmful effects (such as serious vision loss) in people who have taken up to 80,000 IU of beta-carotene per day. The bottom line is: Less is more when it comes to beta-carotene. To be safe I recommend between 12,500 and 25,000 IU of beta-carotene per day from food sources such as carrots” [21].

In my opinion, betacarotene in carrots, however, is safer than even Dr. Sinatra suggests (there is about 12,000 i.u. of betacarotene in one raw carrot). The reason for this is because betacarotene in carrots is attached to lipoproteins which appear to aid in preventing toxicity. Isolated USP betacarotene, even if it allegedly comes from “natural” sources, simply does not have the attached lipoproteins or other potentially protective substances as found in foods like carrots.

Vitamin C in foods exists in at least two distinguishable forms with accompanying food factors [22]. Yet, regular ascorbic acid as well as mineral ascorbates are too incomplete to be properly called vitamin C as they do not contain both forms (i.e., they lack DHAA) and the accompanying food factors [22]! Foods contain both natural forms of vitamin C [22]! Also, foods containing vitamin C are normally less acidic than ascorbic acid.

In vitro studies found that food vitamin C has negative oxidative reductive potential [23], while isolated ascorbic acid had positive ORP [24]. Why is that so important? Because while antioxidants can stop free radical damage, only those substances with proper oxidative reductive potential can actually ‘clean up’ the damage that the free radicals cause. Please understand that “negative ORPs indicate active reducing power, which is immediately capable of antioxidant activity, whereas items with positive ORPs are not” [25]. It should be noted that the Merck Index shows that isolated ascorbic acid has positive redox potential [26].

A Cornell University study found that food vitamin C (as found in whole fruit) was 263 times more eftective as a free radical scavenger than isolated ascorbic acid [27]. This appears to be because fruits contain various naturally occurring phytochemicals are responsible for most of the antioxidant activity [27].

Although ascorbic acid has strong antioxidant effects in vitro, it is even possible isolated ascorbic acid has no in vivo antioxidant effects because “Despite epidemiological and some experimental studies, it has not been possible to show conclusively that higher than anti-scorbutic intake of {SYNTHETIC} vitamin C has antioxidant clinical benefit…{ISOLATED} Vitamin C may be a weak antioxidant in vivo, or its antioxidant actions may have no physiological role, or its role may be small. The oxidative hypothesis is unproven” [28]. Why should people take supplemental synthetic ascorbic acid when it is NOT been proven to have antioxidant effects in humans? On the other hand, high vitamin C containing foods do have proven in vitro and in vivo antioxidant effects [27,29].

One study found that food complex vitamin C had 492 micro moles per gram T.E. (Trolox equivalents) of hydrophilic ORAC (oxygen radical absorbance capacity) [30]—ORAC is essentially a measurement of the ability to quench free radicals (antioxidant ability)—while blueberries (one of the highest ORAC sources [11]) only had 195 micro moles per gram T.E. [30]—thus food complex vitamin C has 2.52 times the ORAC ability of blueberries. Vitamin C containing food has over 15.6 times the ORAC of isolated ascorbic acid [11] (food complex vitamin C is even higher). Actually, there are doubts that isolated ascorbic acid has any significant antioxidant effects in humans [28]. Food vitamin C is clearly superior for any interested in ORAC.


“Cross sectional and longitudinal studies show that the occurrence of cardiovascular disease and cancer is inversely related to vitamin C intake…the protective effects seen in these studies are attributable to fruit and vegetable {FOOD} intake…In general, beneficial effects of supplemental {SYNTHETIC} vitamin C have been noted in small studies, while large well controlled studies have failed to show benefit” [28]. The other quantitative is that in humans, “Plasma is completely saturated in doses of 400 mg and higher daily producing a steady-state plasma concentration of 80 mM…Tissues, however, saturate before plasma” [28]. De-emphasizing vitamin C containing foods by attempting to consume higher quantities of isolated ascorbic acid simply will not have the effects on plasma vitamin C levels, ORP, ORAC, or other health aspects that many consumers of isolated ascorbic acid hope it will [25,28].

So-called ‘natural’ ascorbic acid is made by fermenting refined sugar into sorbitol, then hydrogenating it until it turns into sorbose, then acetone (commonly referred to as nail polish remover) is added to break the molecular bonds which creates ascorbic acid [31]! How ‘natural’ is that?

While it is true that ascorbic acid has certain proven health benefits, no matter how much isolated ascorbic acid one takes orally:

1) It will never saturate plasma and/or tissue vitamin C levels significantly more than can be obtained by consuming sufficient vitamin C containing foods.
2) It will never have negative ORP, thus can never ‘clean-up’ oxidative damage like food vitamin C can.
3) It will never have the free radical fighting capacity of food vitamin C.
4) It will never contain DHAA (the other ‘half’ of vitamin C) or the promoting food factors.
5) It will never have the same effect on health issues, such as aging and cardiovascular disease as high vitamin C foods can.
6) It will not ever be utilized the way food vitamin C is.
7) It will always be a synthetic.

Although vitamin C, “can readily donate electrons to quench a variety of reactive free radical and oxidative species and is easily returned to its reduced state”, simply taking ascorbic acid C with two or three different antioxidants is not enough. Why? Because all free radical and oxidative substances do not get neutralized by all antioxidants.

Vitamin E “as found in foods is [d]-alpha tocopherol, whereas chemical synthesis produces a mixture of eight epimers” [32]. Natural vitamin E has recently been renamed to be called RRR-alpha-tocopherol whereas the synthetic has now been renamed to all-rac-alpha-tocopherol, though supplement labels rarely make this clear; on supplement labels d-alpha-tocopherol is generally ‘natural’, whereas dl-alpha-tocopherol is synthetic [32]. All acetate forms of vitamin E are synthetic. “The antioxidant function of vitamin E cannot be fulfilled by just any antioxidant” [12]. Natural RRR-alpha-tocopherol, which is found in food, has 1.7 – 4.0 times the free radical scavenging strength of the other tocopherols [12]. RRR-alpha tocopherol has 3 times the biological activity of the alpha-tocotrienol form, and synthetic vitamin E simply does not have the same biologic activity of natural vitamin E (some synthetic forms have only 2% of the biological activity of RRR-alpha-tocopherol) [12]. The biologic activity of vitamin E is based on its ability to reverse specific vitamin E-deficiency symptoms [12], therefore it is a scientific fact that, overall, synthetic vitamin E has less ability to correct vitamin E deficiencies than food vitamin E. There is an interesting reason for this, which is that the body regulates plasma vitamin E through a specific liver alpha-tocopherol transfer protein, whereas it has no such protein for other vitamin E forms [12]. Or in other words, the liver produces a protein to handle vitamin E found in Food, but not for the synthetic forms!

The body retains natural vitamin E 2.7 times better than synthetic forms [33]—it attempts to rid itself of synthetic forms as quickly as possible [33]. Vitamin E has been shown to reduce the risk of various cancers, coronary heart disease, cataract formation, and even air pollution [12,34]. It also is believed it may slow the aging process and decrease exercise-induced oxidative stress [12,34]. Artificial fats seem to increase the need for vitamin E [35]. Vitamin E content is highest in oils such as soy, but is also relatively high in rice bran [36].

Both chemical form and source of vitamin E may play a role as “chemically synthesized alpha-tocopherol is not identical to the naturally occurring form” [12]. Thus those who claim that a synthetic vitamin, even when it is in the same “chemical form” (it is never in the same actual form due to the presence of food constituents), is as good as one in a natural, food form, are simply overlooking the scientific facts about vitamins.

Food vitamin E, as found in specially grown rice, has been proven to have 12 micro moles per gram T.E. of lipophilic ORAC (oxygen radical absorbance capacity) [57]—ORAC is essentially a measurement of the ability to quench free radicals (antioxidant ability). It is interesting to note that so-called “natural” forms (like succinate) do not even work like food vitamin E. Even though many consider d-alpha-tocopherol as the best (isolated) natural form of vitamin E, the PDR notes, “d-Alpha-Tocopherol succinate itself has no antioxidant activity” [16] so why would anyone want that for their vitamin E supplement?

High dose isolated vitamin E can have pro-oxidant effects [37]. Jerome Block (M.D.) reports, “My research of the literature and my patients supports that this {ISOLATED} vitamin E supplement by itself does not supply adequate antioxidant protection…If one takes the {ISOLATED} commercial form of vitamin E…there is evidence that the effect of the antioxidant is not present…vitamin E found in foods is much more effective than the single alpha-tocopherol supplements…Although vitamin E has an excellent safety record, studies show that alpha-tocopherol alone…has been pro-oxidant rather than antioxidant” [38]. Food vitamin E, which has proven antioxidant abilities [12], is clearly superior to the isolated versions.

Selenium is a mineral with antioxidant abilities and is also “a necessary mineral for the production of antioxidants in the body” [27]. The three most common forms of selenium in supplements are sodium selenite, seleniomethionine, and food selenium. The predominant form of selenium found in the body and in food selenium is selenocysteine [39]. Human research suggests that food selenium is less toxic than industrial/mineral salt form [39].Food selenium (which is normally a specially grown yeast food) should not be confused with yeasts which have been simply fortified with sodium selenite, which can be quite toxic. Sodium selenite is not a food, but is the result of combining sodium hydroxide and selenious acid; sodium selenite is commonly used to remove green color from glass during glass manufacturing [26]. Why would anyone want to take that as part of their antioxidant supplement?

One study using 247 mcg/day of high-selenium yeast found that plasma selenium levels were 2-fold higher than baseline values after 3 and 9 months and returned to 136% of baseline after 12 months, whereas there was a 32% increase in blood glutathione levels also seen after 9 months. This change coincided with a 26% decrease in protein-bound glutathione and a 44% decrease in the ratio of protein-bound glutathione to blood glutathione. The changes in glutathione and protein-bound glutathione were highly correlated with changes in plasma selenium levels and were believed to reflect a reduction in oxidative stress [40].

It has been reported that food selenium seems to reduce toxicity associated with cisplatin chemotherapy [41], hence many people take it when undergoing conventional cancer treatments. Furthermore, Larry Clark, Ph.D. and others have found that selenium in yeast appears to reduce risk of certain cancers [42]. Julian Whitaker, M.D. reports, “The best absorbed form of selenium, and the one used by Dr. Clark’s research, is high-selenium yeast” [42].

Food selenium is about twice as well retained as non-food forms [13,40].

Zinc is an important component of superoxide dismutase (see below). “Dietary zinc has potent antioxidant and anti-inflammatory properties” [43]. Additionally, “Poor zinc nutrition may be an important risk factor in oxidant release and the development of DNA damage and cancer. Approximately 10% of the United States population ingests <50% of the recommended daily allowance for zinc, a cofactor in proteins involved in antioxidant defenses, electron transport, DNA repair and p53 protein expression” [44].

High zinc-containing foods include wheat bran, beef, miso, spinach, mushrooms, alfalfa sprouts, brewer’s yeast, turkey, lamb, bean sprouts, tofu, and to a lessor degree in whole wheat bread [45] (shellfish also contains zinc, but this researcher cannot recommend that as a source). Zinc in unleavened whole wheat bread is less bioavailable than zinc in whole wheat bread leavened with yeast [15]; enzymatically-processed food grade yeast seems to contain some of the most bioavailable food zinc. Research also suggests that certain food forms of zinc are better absorbed and retained than non-food forms [15,16].

Superoxide Dismutase

Superoxide dismutase (S.O.D.) is naturally found in foods such as nutritional yeast and barley green. It is not considered to be an essential nutrient, nor is it an herb (though it does exist in plants). However, S.O.D. “is one of the most important enzymes that functions as a cellular antioxidant…The absence of this enzyme is lethal” [46]. Although S.O.D. (like glutathione, lipoic acid, etc.) is not a vitamin/mineral it is listed here separately because it may be the single most important antioxidant (it is possible that some other antioxidant will take over that role, but more studies appear to have been published about S.O.D. than possibly any other non-vitamin, non-mineral antioxidant).

“It protects intracellular components from oxidative damage, converting the superoxide ion to hydrogen peroxide” [47]. S.O.D. appears to be able to prevent activation of “phospholipase A2 and proanoid synthesis by scavenging free radicals, thereby reducing lipid peroxidation products” [48]. It is a powerful free radical scavenger, which has been clinically shown to protect the brain, heart, liver, lungs, kidneys, skin, muscles, penis, nerves, and spinal cord from ischemic injury [48].

S.O.D. has been shown to inhibit articular tissue damage associated with osteoarthritis [49], decreases lipid peroxidation in damaged skin cells [50], protect against late radiation-induced tissue injury [51], improves clinical symptoms associated with Bechet’s syndrome [52], helps protect the retina [53], helps protect against iron toxicity [54], inhibits vasogenic brain edema after brain injury [55], increases flu survival rates in mice [56], plays a role in bacterial defense [57], helps normalize blood pressure [58,59] helpful for cardiovascular problems [48,60,61], reduces LDL oxidation involved in atherosclerosis [61], is reduced in Alzheimer’s patients [62], improves sperm motility [63], and even helped patients with TMJ who did not respond to traditional therapy [64]; there over a thousand recent (within the last 5 years) peer-reviewed papers on S.O.D. High levels of S.O.D. have been associated with reduced growth of Candida albicans [65]. It is often sold in a “purified” version (from animal products) as an antiaging product [44]; S.O.D. seems to have “antiaging” properties [48]. Ingestion of polyethylene glycol-conjugated superoxide dismutase is not as effective as CuZn (copper/zinc) superoxide dismutase [66,67]. CuZn superoxide dismutase, along with Mn superoxide dismutase [68] exists naturally, in foods such as nutritional yeast (Saccharomyces cerevisiae).

Antioxidant Herbs

There are many antioxidant plants and other herbs. All antioxidants in plants and herbs exist in their natural food forms, hence (unless isolated) are true antioxidants. The following list is not exhaustive (and intentionally does not include green tea as the caffeine it contains is a problem for some):

Barley Grass Concentrate contains a variety of antioxidant substances, including natural S.O.D. (see Superoxide dismutase earlier in this paper) which is also able scavenge reactive oxygen species [69,70]. “Research at the University of California Davis has demonstrated that a flavonoid in barley grass known as 2-0-glycosylisovitexin (2-0-GIV) is a potent antioxidant which is more powerful than other antioxidants in protecting against fat oxidation (lipid peroxidation) in human cells’ [71]. Others state, “the major flavonoid antioxidants in young green barley leaves are in fact the flavone-C-glycosides, saponarin and lutonarin” [72]. Barley grass (like wheat grass and other green plants) also contains chlorophyll, which has antioxidant ability [15].

Carrots provide betacarotene (see Betacarotene earlier in this paper) and other antioxidant carotenoids. Carrots also contain “xanthophyll, a very powerful anticancer phytochemical” [71]. Carrots are one the vegetables with high total antioxidant activity [5].

Citrus Fruits, which are common in Western diets, contain a variety of antioxidants such as flavonoids [15] and food vitamin C (see Vitamin C above). Citrus fruits have been shown to have significant antioxidants in vivo (and in vitro) [5]. Pink grapefruit is a source of lycopene (as are tomatoes) [15]. The peel and pulp of citrus has more of the flavonoid hesperidian than the juice [15].

Eleuthro Root, which was formerly called Siberian Ginseng, is an adaptagen, which means that it helps the body deal with various forms of stress [73]. It has been found to have “strong antioxidant against scavenging on DPPH free radical and also ethyl acetate fractionation exhibited high antilipid peroxidative activities. In the cytotoxic effects were evaluated on seven human cancer cell lines, the values of 50% growth inhibition (GI(50)) were mostly below 30 microg/ml for crude extracts to be considered as significantly active” [74]. A Russian study found that it had strong antioxidant abilities [75].

Ginger Root has constituents with antioxidant effects and can improve peripheral circulation [73]. Specifically it has at least “four shogaols that protect IMR32 human neuroblastoma and normal human umbilical vein endothelial cells from beta-amyloid(25 – 35) insult at EC50 = 4.5 – 81 microM” [76]. Ginger is one of the plants that contain the most antioxidants [77].

Ginkgo Leaf contains about 40 different bioflavonoids, including proanthocyanidins (see Grape Seed/Skin extract below) and quercetin, that “act as free radical scavengers” [73]. “Quercitin is a phenolic antioxidant that and has been shown to inhibit lipid peroxidation” in vitro, but it may need food substances to be an effective antioxidant in vivo [15]. “Cerebral insufficiency many cause anxiety and stress, memory, concentration, and mood impairment, and hearing disorders, all of which may benefit from ginkgo therapy” [73]. “Recent studies conducted with various molecular, cellular and whole animal models have revealed that leaf extracts of Ginkgo biloba may have anticancer (chemopreventive) properties that are related to their antioxidant, anti-angiogenic and gene-regulatory actions. The antioxidant and associated anti-lipoperoxidative effects of Ginkgo extracts appear to involve both their flavonoid and terpenoid constituents…In humans, Ginkgo extracts inhibit the formation of radiation-induced (chromosome-damaging) clastogenic factors and ultraviolet light-induced oxidative stress – effects that may also be associated with anticancer activity. Flavonoid and terpenoid constituents of Ginkgo extracts may act in a complementary manner to inhibit several carcinogenesis-related processes, and therefore the total extracts may be required for producing optimal effects” [78]. Ginkgo biloba extracts, “could reduce cytokine-stimulated endothelial adhesiveness by downregulating intracellular reactive oxygen species formation, nuclear factor-kappaB and activator protein 1 activation, and adhesion molecule expression in HAECs, supporting the notion that the natural compound Ginkgo biloba may have potential implications in clinical atherosclerosis disease” [79].

Grape Seed/Skin Extract contains a variety of antioxidant substances and is over 90% proanthocyanidins, which are a type of bioflavonoid with powerful free radical fighting ability [73]. “Oligomeric proanthocyanidins, naturally occurring antioxidants widely available in fruits, vegetables, nuts, seeds, flowers and bark, have been reported to possess a broad spectrum of biological, pharmacological and therapeutic activities against free radicals and oxidative stress. We have assessed the concentration- or dose-dependent free radical scavenging ability of a novel IH636 grape seed proanthocyanidin extract (GSPE) both in vitro and in vivo models, and compared the free radical scavenging ability of GSPE with {ISOLATED} vitamins C, E and beta-carotene. These experiments demonstrated that GSPE is highly bioavailable and provides significantly greater protection against free radicals and free radical-induced lipid peroxidation and DNA damage than vitamins C, E and beta-carotene. Oxidative tissue damage was determined by lipid peroxidation and DNA fragmentation, while apoptotic cell death was assessed by flow cytometry. GSPE provided significantly better protection as compared to vitamins C and E, singly and in combination. GSPE also demonstrated excellent protection against acetaminophen overdose-induced liver and kidney damage by regulating bcl-X(L) gene, DNA damage and presumably by reducing oxidative stress. GSPE demonstrated excellent protection against myocardial ischemia-reperfusion injury and myocardial infarction in rats. GSPE was also shown to upregulate bcl(2) gene and downregulate the oncogene c-myc. Topical application of GSPE enhances sun protection factor in human volunteers, as well as supplementation of GSPE ameliorates chronic pancreatitis in humans. These results demonstrate that GSPE provides excellent protection against oxidative stress and free radical-mediated tissue injury” [80]—it should be noted that this study compared against isolated (non-food) vitamins and isolated betacarotene. Interestingly it is believed that “grape-skin extract may have a sparing effect on vitamin C” in human plasma [81]. Grape seeds, but mainly grape skin, contains resveratrol which has antioxidant abilities and may be “associated with a reduced incidence of cardiovascular disease and a reduced incidence of cancer” [15]. Resveratrol is prized by many for its anti-aging properties and “has recently been found to possess glutathione-sparing activity” [15].

Kudzu Root contains a powerful antioxidants, including an isoflavone known as puerarin [82]. “Kudzu was found to be an effective adsorbent for basic dye colour removal” [83]. Kudzu and puerarin are being investigated for their apparent ability to suppress alcohol desire for alcoholics [84]; it is also being investigated for its ability to glucose control for diabetics. One study found that kudzu in crude form appears to have greater antioxidant effects than isolated puerarin [85].

Milk Thistle Seed contains silymarin, which is a polyphenolic antioxidant flavonoid [17]. “Silymarin is an antihepatotoxic substance isolated from fruits of Silybum marianum. Possibly due to their antioxidant and membrane stabilizing properties, the compounds have been shown to protect different organs and cells against a number of insults” [86]. Silybinin is a component of silymarin and has been shown to reduce lipid peroxidation [87]. Furthermore, “silibinin inhibits the growth of human prostate cancer cells (PCA) both in vitro and in vivo” [88].

Rosemary Leaf contains flavonoid antioxidants [71] and can “increase detoxification of carcinogens” in certain instances [73]. It contains such flavonoids as cirismarin, diosmin, hesperidin, homoplantiginin, and phegopolin [89]. Topically, rosemary is used to promote wound healing and as an analgesic for myalgias and neuralgias [89].

Saccharomyces cerevisiae, also known as nutritional yeast, contains antioxidants such as S.O.D. (see above) and glutathione (actually most isolated glutathione comes from fermented yeast [15]). Certain food antioxidant nutrients grown in Saccharomyces cerevisiae, such as zinc and selenium have been shown to have higher antioxidant effects and/or better absorption than the isolated mineral salt versions that are commonly sold [13,14,35,43,45]. Saccharomyces cerevisiae also naturally contains protein chaperones, which are essential for mineral absorption. Saccharomyces cerevisiae also stimulates phagocytosis [89]. The bioavailability of coenzyme q10 (a substance with antioxidant properties) is enhanced when it is in a media containing Saccharomyces cerevisiae [90].

Schisandra Fruit “has pronounced liver protective effects” [73] and strong antioxidant activity [91]. Schisandra contains at least 9 dibenzocyclooctene lignans, “Seven of the 9 lignans (1 mM) inhibited iron/cysteine-induced lipid peroxidation (malondialdehyde, MDA, formation)…The actions of the 7 lignans were much more potent than vitamin E at the same concentration of 1 mM. Among the lignans, schisanhenol was the most active one. This compound also prevented the decrease of membrane fluidity of liver microsomes induced by iron/cysteine. The results indicated that seven of the lignans such as schisanhenol have anti-oxidant activities” [91].

Tomatoes are a source of lycopene [15] and food vitamin C [21]. “Lycopene is a member of the carotenoid family…[and] is responsible for the red color of red tomatoes” [15]. “In vitrostudies have demonstrated that lycopene has the highest antioxidant activity of all the carotenoids” [15]. Yet, it does not seem to have the same effect in vivo as tomatoes themselves do. One recent study that compared tomatoes to isolated lycopene found that tomatoes inhibited prostate carcinogenesis but that lycopene did not [92].

Turmeric Root contains curcuminoids which have antioxidant and cancer-inhibiting properties [73]. Many “laboratory studies have identified a number of different molecules involved in inflammation that are inhibited by curcumin including phospholipase, lipooxygenase, cyclooxygenase 2, leukotrienes, thromboxane, prostaglandins, nitric oxide, collagenase, elastase, hyaluronidase, monocyte chemoattractant protein-1 (MCP-1), interferon-inducible protein, tumor necrosis factor (TNF), and interleukin-12 (IL-12)” [93].

Water Thyme is one of the most mineral-dense foods and contains nutritional antioxidants, including vitamin C (see Vitamin C above) and chlorophyll. It is sometimes included in food antioxidant formulas.

Conclusion

Herbs and plants containing antioxidants offer unique benefits, which have not been synthetically duplicated.

Actually, no matter how much synthetic vitamins or industrially-processed rock ‘nutrients’ one takes orally, they will:

1) Never be a truly complete nutrient source.
2) Never replace all the functions of food/herbal vitamins and minerals.
3) Always be unnatural substances to the body.
4) Always strain the body by requiring that it detoxify or somehow dispose of their unnatural structures/chemicals.
5) Never be utilized, absorbed, and retained the same as food/herbal nutrients.
6) Not be able to prevent advanced protein glycation end-product formation the same as food/herbal nutrients.
7) NEVER BE ABLE TO HAVE THE PROVEN ANTIOXIDANT EFFECTS THE SAME AS FOOD NUTRIENTS.
8) Always be industrial products.
9) Always be composed of petroleum-derivatives, hydrogenated sugars, and/or industrially-processed rocks.
10) Never build optimal health the same as food nutrients.

The standards of naturopathy agreed to in 1947 (at the Golden Jubilee Congress) included the statements, “Naturopathy does not make use of synthetic or inorganic vitamins…Naturopathy makes use of the healing properties of…natural foods, organic vitamins” [94]. Even back in the 1940s, professionals interested in natural health recognized the value of food, over non-food, vitamins.

Although many studies have demonstrated that isolated nutrients such as betacarotene, ascorbic acid, and alpha-tocopherol do have significant antioxidant effects in test tubes (in vitro), more recent research has raised serious questions as to whether these chemical isolates have significant antioxidant effects in humans (in vivo) [15,23,33]. Furthermore, in 1999 the Nobel prize for medicine was awarded to Gunter Blobel who discovered that nutritional minerals need protein chaperones for absorption. Such protein chaperones do not exist in mineral salt forms which are commonly included in ‘antioxidant’ or multivitamin formulas. Protein chaperones do, of course, exist in foods such as Saccharomyces cerevisiae [95,96].

While it is known that diets focused on foods high in antioxidants can help prevent cancers [3], synthetic antioxidants appear to be so ineffective that they may actually increase cancer risk [6]. Additionally, regarding cancer and other diseases, “The available evidence points to the benefits of food-derived antioxidants, but more evidence is needed before {ISOLATED} antioxidant…supplementation can be routinely recommended” [97]. “A predominantly plant-based diet reduces the risk for development of several chronic diseases. It is often assumed that antioxidants contribute to this protection, but results from intervention trials with single antioxidants administered as supplements quite consistently do not support any benefit. Because dietary plants contain several hundred different antioxidants” [77], it makes sense to consume food antioxidants and not individual, isolated ones.

Although some scientists think isolated nutrients have questionable and even negative effects, “It is doubtful that antioxidant-rich foods would have a negative impact on brain aging” [9]—or anything else for that matter. Humans are supposed to eat foods and not consume isolated USP nutrients (even if they are called ‘natural’ and even if they are called ‘antioxidants’). Since all free radical and oxidative substances do not get neutralized by all antioxidants, it makes sense to consume a variety of plants and/or antioxidant containing herbs—plants which contain hundreds of antioxidant compounds [15,77,89].

“Unfortunately, a single purified substance will not always have the same antioxidant activity, nor provide the same clinical benefits as…combinations occurring in natural extracts” [98]. Some of these ‘purified’ substances have been shown to sometimes have pro-oxidant instead of antioxidant effects [19,20,32,33].

Why would anyone want to take isolated ‘antioxidants’ instead of foods or those antioxidant formulas which are only composed of 100% food?

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[57] San Mateo LR, Hobbs MM, Kawula TH. Periplasmic copper-zinc superoxide dismutase protects Haemophilus ducreyi from exogenous superoxide. Mol Microbiol,1998;27(2):391-404

[58] Zhang XM, Ellis EF. Effects of superoxide dismutase decreases mortality, blood pressure, and cerebral blood flow responses induced by acute hypertension in rats. Chung Kuo Yao Li Hsueh Pao,1990;11(4):324-328

[59] Przyklenk K, Kloner RA. Superoxide dismutase plus catalase improve contractile function in the canine model of the stunned myocardium. Circulatory Res,1986;58(1):148-156

[60] Nelson SK, Bose SK, McCord JM. The toxicity of high dose superoxide dismutase suggests that superoxide can both initiate and terminate lipid peroxidation in the reperfused heart. Free Radic Biol Med,1994;16(2):195-200

[61] Wang P, et al. Overexpression of human copper, zinc-superoxide dismutase (SOD1) prevents postischemic injury. Proc Natl Acad Sci U S A,1998;95(8):4556-4560

[62] De Deyn PP, et al. Superoxide dismutase activity in cerebrospinal fluid of patients with dementia and some other neurological disorders. Alzheimer Dis Assoc Discord,1998;12(1):26-32

[63] Kobayshi T, Miyazaki T, Natori M, Nozawa S. Protective role of superoxide dismutase in human sperm motility: superoxide dismutase activity and lipid peroxide in human seminal plasma and spermatozoa. Hum Reprod,1991;6(7):987-991

[64] Lin Y, et al. Use of superoxide dismutase (SOD) in patients with temporomandibular joint dysfunction. Intl J Oral Maxillofac Surg,1994;23(6pt2):428-429

[65] Romandini P, Bonotto C, Bertoloni G, Beltramini M, Salvato B. Superoxide dismutase, catalase and cell dimorphism in Candida albicans cells exposed to methanol and different temperature. Comp Biochem Physiol Pharm Toxicol Endocrinol,1994;108(1):53-57

[66] Haun SE, Kirsch JR, Helfaer MA, Kubos KL, Traystman RJ. Polyethylene glycol-conjugated superoxide dismutase fails to augment brain superoxide dismutase activity in piglets. Stroke,1991;22(5):655-659

[67] Tibell L, Aasa R, Marklund SL. Spectral and physical properties of human extracellular superoxide dismutase: a comparison with CuZn superoxide dismutase. Arch Biochem Biophys, 1993;304(2):429-433

[68] Turi TG, Kalb VF, Loper JC. Cytochrome P450 lanosterol 14 alpha-demethylase (ERG11) and manganese superoxide dismutase (SOD1) are adjacent genes in Saccharomyces cerevisiae. Yeast,1991;7(6):627-630

[69] Cremer L, Herold A, Avram D, Szegli G. A purified green barley extract with modulatory properties upon the TNF alpha and ROS released human specialised cells isolated from RA patients. Roum Arch Microbiol Immunol 1998;57(3-4):231-242

[70] Yu YM, Chang WC, CHang CT, Hsieh CL, Tsai CE. Effects of young barley leaf extract and antioxidative vitamins on LDL oxidation and free radical scavenging activities in type 2 diabetes. Diabetes Metab 2002;28(2):107-114

[71] Duarte A. Health Alternatives. Megasystems, Morton Grove (IL), 1995

[72] Markham KR, Mitchell KA. The mis-identification of the major antioxidant flavonoids in young barley (Hordeum vulgare) leaves. Z Naturforsch [C] 2003;58(1-2):53-56

[73] DerMarderosian A, editor. The Review of Natural Products, 1st ed. Facts and Comparisons, St. Louis, 2001

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[75] Bol’shakova IV, Lozovskaia EL, Sapezhinskii II. Antioxidant properties of a series of extracts from medicinal plants. Biofizika. 1997 Mar-Apr;42(2):480-483

[76] Kim DS, Kim DS, Oppel MN. Shogaols from Zingiber officinale protect IMR32 human neuroblastoma and normal human umbilical vein endothelial cells from beta-amyloid(25-35) insult. Planta Med. 2002;68(4):375-376

[77] Halvorsen BL, Holte K, Myhrstad MC, Barikmo I, Hvattum E, Remberg SF, Wold AB, Haffner K, Baugerod H, Andersen LF, Moskaug O, Jacobs DR Jr, Blomhoff R. A systematic screening of total antioxidants in dietary plants. J Nutr. 2002 Mar;132(3):461-471

[78] DeFeudis FV, Papadopoulos V, Drieu K. Ginkgo biloba extracts and cancer: a research area in its infancy. Fundam Clin Pharmacol. 2003;17(4):405-417

[79] Chen JW, Chen YH, Lin FY, Chen YL, Lin SJ. Ginkgo biloba Extract Inhibits Tumor Necrosis Factor-{alpha}-Induced Reactive Oxygen Species Generation, Transcription Factor Activation, and Cell Adhesion Molecule Expression in Human Aortic Endothelial Cells. Arterioscler Thromb Vasc Biol. 2003; 23(9):1559-1566

[80] Bagchi D, Bagchi M, Stohs SJ, Das DK, Ray SD, Kuszynski CA, Joshi SS, Pruess HG. Free radicals and grape seed proanthocyanidin extract: importance in human health and disease prevention. Toxicology. 2000;148(2-3):187-197

[81] Young JF, Dragsted LO, Daneshvar B, Lauridsen ST, Hansen M, Sandstrom B. The effect of grape-skin extract on oxidative status.Br J Nutr. 2000;84(4):505-513

[82] Guerra MC, Speroni E, Broccoli M, Cangini M, Pasini P, Mingett A, Crespi-Perellino N, Mirasoli M, Cantelli-Forti G, Paolini M. Comparison between Chinese medical herb Peuraria lobata crude extract and its main isoflavone puerarin antioxidant properties and effects on rat liver CYP-catalased drug metabolism. Life Sci 2000;67(24):2997-3006

[83] Allen SJ, Gan Q, Matthews R, Johnson PA. Comparison of optimised isotherm models for basic dye adsorption by kudzu. Bioresour Technol. 2003;88(2):143-152

[84] Rezvani AH, Overstreet DH, Perfumi M, Massi M. Plant derivatives in the treatment of alcohol dependency. Pharmacol Biochem Behav. 2003;75(3):593-606

[85] Guerra MC, Speroni E, Broccoli M, Cangini M, Pasini P, Minghett A, Crespi-Perellino N, Mirasoli M, Cantelli-Forti G, Paolini M. Comparison between chinese medical herb Pueraria lobata crude extract and its main isoflavone puerarin antioxidant properties and effects on rat liver CYP-catalysed drug metabolism. Life Sci. 2000;67(24):2997-3006

[86] Kvasnicka F, Biba B, Sevcik R, Voldrich M, Kratka J. Analysis of the active components of silymarin. J Chromatogr A. 2003;990(1-2):239-245

[87] Shimizu I. Antifibrogenic therapies in chronic HCV infection. Curr Drug Targets Infect Disord. 2001;1(2):227-240

[88] Dhanalakshmi S, Agarwal P, Glode LM, Agarwal R. Silibinin sensitizes human prostate carcinoma DU145 cells to cisplatin- and carboplatin-induced growth inhibition and apoptotic death. Int J Cancer. 2003 Sep 20;106(5):699-705].

[89] Gruenwald J, Brendler T, Jaenicke C, ed. PDR for Herbal Medicine, 2 nd ed. Medical Economics, Montvale (NJ) 2000

[90] Kurowska EM, Dresser G, Deutsch L, Bassoo E, Freeman DJ. Relative bioavailability and antioxidant potential of two coenzyme q10 preparations. Ann Nutr Metab. 2003;47(1):16-21

[91] Lu H, Liu GT. Anti-oxidant activity of dibenzocyclooctene lignans isolated from Schisandraceae. Planta Med 1992;58(4):311-313

[92] Boileau TW, Liao Z, Kim S, Lemeshow S, Erdman JW, Clinton SK. Prostate carcinogensis in N-methyl-N-nitrosourea (NMU) testosterone-treated rats fed tomato powder, lycopene, or energy restricted diets. J Natl Cancer Inst 2003;95(21):1578-1586

[93] Chainani-Wu N. Safety and anti-inflammatory activity of curcumin: a component of tumeric. J Altern Complement Med. 2003;9(1):161-168

[94] Gehman JM. From the Office of the President: Pseudo-Group Once Again Misleading the Naturopathic Field. Official Bulletin ANA, January 25, 1948:7-8

[95] Rouhi AM. Escorting metal ions: protein chaperone protects, guides, copper ions in transit. Chem Eng News, 1999;11:34-35

[96] Himelblau E, et al. Identification of a functional homolog of the yeast copper homeostasis gene ATX1 from Arabidopsis. Plant Physiol 1998;117(4):1227-1234

[97] Adams AK, Best TM . The Role of Antioxidants in Exercise and Disease Prevention. Physician & Sportsmed, 2002;30(5):37-46

[98] Hardy G, Hardy I, Ball PA. Nutraceuticals – a pharmaceutical viewpoint: part II. Curr Opin Clin Nutr Metab Care. 2003;6(6):661-71

Some of these studies (or citations) may not conform to peer review standards. Therefore, the results are not conclusive. Professionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA. All products distributed by Doctors’ Research, Inc. are nutritional and are not intended for the treatment or prevention of any medical condition.

Why are Synthetics Sold as Imitations of Natural Foods and Drugs?

If you have read this far, you probably have already asked yourself that question.  Instead of me trying to answer that, I felt it might be helpful to know that this question was raised a half-century ago.  To answer it, Dr. Royal Lee, in 1948, wrote the following paper which he titled, How and Why are Synthetic Poisons Sold as Imitations of Natural Foods and Drugs?, “

An honestly enforced food and drug law is just as essential to the proper operation of commerce in foods and drugs as the rules and an umpire to administer them in a ball game.

It is obvious to all that such a law should stop the sale of poisonous imitations of common foods and drugs, except where proper labeling warns the buyer of just what he is getting, New synthetic products are constantly appearing, and are sold without proper tests or proper in­vestigation of what their real proper‑ties are.

In fact, the Food & Drug laws seem to be suspended where synthetic imitations of good foods are concerned, and often actually perverted to persecute makers and sellers of real products, as we shall later show.

Let us first get to the bottom of this question of how synthetic products differ from natural. There are two ways in which a difference may exist:

a.   The synthetic product may not be the same thing, but something that resembles the natural product.
b.   The synthetic product is always a simple chemical substance, while the natural is a complex mixture of related and similar materials.

The first situation, where the synthetic material is not the same thing, is common. Take lactic acid, originally made from sour milk, now made synthetically in large quantities. The sour milk lactic‑acid consisted entirely of molecules that were of a right‑handed character. The synthetic is a mixture of equal parts of right‑handed molecules (dextro‑lactic acid) and left­-handed molecules (laevo‑lactic acid). Such mixtures are known as racemic compounds. (In catalogs, etc., the prefixes I‑, d‑, or r‑, are used before the name of the substance.)

About thirty years ago, Dr. Crofton, an English endocrinologist explained how digestive enzymes could only act upon part of the food available. Here are his words:

“It will not be unprofitable now to inquire into the raison d’etre of this curious adaptor mechanism. How is it that the ferments of the tissue‑cells themselves cannot deal with the comparatively simple food material presented to them without the aid of adapters?

Pasteur first discovered that there are certain compounds of carbon which, while identical in every other respect having the same chemical formulae and the same chemical reactions differ only in their behavior to polarized light, that is one compound rotated the light to the right, the other to the left. Such compounds have the same specific gravity, molecular volume melting point, solubility, heat of solution, of combustion and of neutralization. They have the same amount of chemical affinity and index of refraction. Their absorption spectra are the same, and they have the same chemical action, yet one body rotates the light to the right as much as the other to the left. Pasteur’s discovery was made with ammonium tartrates, and he found that if the common mould penicillium glaucum was made to grow in a solution of both (ammonium racemate) it lived on the dextro‑isomer but left the levo‑salt, as he thought, quite untouched, But it now appears it is broken up to a small extent.”[1] (This requirement of the living cell for a minute amount of the laevo‑salt, and the reason for their requirement for the major amount to be the dextro‑ form is explained by Lee and Hanson in their discussion of cell reactions in their book, “Protomorphology”, 1947, Lee Foundation [2].)

Few people know that dextro‑lactic acid is a food and laevo‑lactic acid is a poison. (One is converted into sugar in digestion, the other is a waste product.) Lactic acid once was found useful as a source of carbohydrate as a milk modifier for babies., and began to get into use in special cases where sugars were not well tolerated. In Halifax, some time ago, a number of babies died from the administration of lactic acid in milk, and here was a case where the synthetic product was inadvertently used in place of the natural, because of inadequate labeling precautions. [3] The doctors who recommended its use probably did not even know that there was a difference between the synthetic and natural lactic acid, although the drug catalog of Eli Lilly and Company of 1938, page 195, offers some information on the subject. The basic trouble is that the makers of synthetic products do not want a stigma of inferiority to be put on their imitation products, and will not label their imitations as different unless forced by conscientious food and drug inspectors to do so. And it is a notorious fact that the law is being ignored in many ways.

Where a food product must be composed of, say right‑handed molecules, the left‑hand may be as useless as in the case of left and right hand bolts and nuts in machinery. If you needed right hand cap screws to put the head of your auto engine back on, left hand screws would only serve to cause confusion and probably a failure to get the machine back into operation, unless you could find among them enough of the right screws to finish the job. To feed racemic or wrong “handed” food products is just as foolish. In the case of the babies in Halifax it caused death to feed the racemic product.

In 1895 Paul Walden, of the University of Rostock, (Germany), announced his discovery of the ‘Walden Effect,” the phenomena of the alteration of the optical inversion of natural organic substances that had been isolated M‑ crystal purity, over a period of time, apparently a result of removal from their normal environment and association with other protective and colloidal factors.

Walden, in a series of lectures at Cornell University, (1927‑28), stated:

“The phenomenon of autoracemization is of interest in connection with the question of permanency of optically active substances. Let us consider a pure organic substance such as the dextrorotatory bromo‑succinic ester. When it is kept for some time in a closed flask at ordinary temperatures, it undergoes spontaneous intramolecular rearrangement and a gradual decrease of the optical rotation results; in other words, it racemizes. Several examples may be cited to illustrate this remarkable fact…Might we
not speak of ‘dying molecules’ much as we speak of ‘dead catalysts’?… The effect of
these reactions is, as we may express it, a complete turning ‘inside out’ of the molecule.”

Dr. Emil Fischer, in 1906, said:

“This discovery is the most surprising observation in the field of optically active substances since the fundamental investigations of Pasteur.”

Amino acids are also useless if not toxic when present in synthetic forms. only left handed (laevo‑) amino acids can be assimilated. All synthetic aminos are racemic.

Adrenalin is an outstanding example of a synthetic product that is being commercialized in disregard of the difference in physiological action. The natural adrenalin is fifteen times as 35 active as the synthetic dextro form [4] in its effect on blood vessels, while the dextroadrenalin is eighteen times as effective in promoting glycosuria.

Now, since the commonest use of adrenalin is to promote the vascular changes that relieve the asthmatic patient, the glycosuria (diabetes promoting) effect is definitely not wanted. But to get the same vascular effect, 15 x 18 or 270 times as much of the synthetic stuff must be used, in terms of its unwanted effect of putting sugar into the urine.[5]

The cost of calling a doctor and of getting a shot of adrenalin by the asthmatic patient when he is struggling for a breath of air is far too much to offset the two‑cent saving made by the pharmaceutical manufacturer who puts synthetic adrenalin in the ampule used by that doctor. But, if neither the doctor or the patient knows the difference, the synthetic stuff certainly win be the one he gets. Although natural adrenalin can be made as a by‑product in the processing of glands in making adreno‑cortin, makers of this material tell us there is no market for natural adrenalin because of the low price of the synthetic product.

Pantothenic acid is a vitamin now commercially available only in the synthetic form. Probably this is the reason for its effect of causing a loss of sex function, particularly in females. This castrating action has been found both in test animals and in human patients receiving the “vitamin”, according to unpublished reports to us.

Pure natural Vitamin E was found three times as potent as pure synthetic Vitamin E.[6]

Of course, the poisonous nature of the synthetic Vitamin D sold as “Viosterol” and “Vigantol” is well established. It causes blood in the urine very quickly in children, by its destructive action to the kidneys. Deaths have been reported from the ordinary dosages used to “protect” from rickets. [7]

WHY DO NOT THE PEOPLE AND MEDICAL MEN KNOW THESE FACTS? Is it because the commercial promoters of cheap imitation food and drug products spend enough money to stop the leaking out of information?

Here is a good example of how hard it is to get the facts. In “Good Housekeeping” for September, 1943, in the “Question Box”‘ department, the question was asked, “Are synthetic vitamins as beneficial as those from food sources?” The answer was made “Manufactured vitamins are identical with those found in foods. They are just as beneficial.

When asked what references they could offer to substantiate that statement, “Good Housekeeping quoted the journal of the American Medical Association, December . 21, 1940, page 2185: ‘There is no detectable difference between the synthetic chemical vitamin and the natural ones. Ascorbic acid is just as good Vitamin C as one gets from an orange.”

When pressed for actual experimental evidence instead of swivel chair opinions, the Editor of “Good Housekeeping” referred the question to a group of “experts.” Here are their opinions:

Dr. E. V. McCollum of Johns Hopkins:”…each and every one of these synthetic vitamins is identical with the natural product.”

Dr. Henry C. Sherman, Columbia University: “In some cases the natural and synthetic forms seem to be identical while in other cases there may be more than one natural or more than one synthetic form.” When asked for factual evidence from experimental work to prove that the synthetic vitamins in “enriched” flour, were equal to the natural, he replied, “I think any answers that a scientific worker would give you would be based upon facts and that nothing would be gained by spending time on library researches in order to attach specific references to our answers.”

Dr. George R. Cowgill, Yale University School of Medicine: “In answering the question raised in your letter about relative values of synthetic as compared with “natural” vitamins one should keep clearly in mind the meaning of the terms involved. There is no difference between these two sources of the vitamins as such. However, in many nutritional experiments one works with highly artificial diets containing the synthetic vitamins and there is no supply of various unknown factors that are needed for nutrition. If these unknown factors are missing, obviously some malnutrition will result, but it seems clear in this situation that one is not thereby justified in concluding that the synthetic vitamins are inferior to the “natural” vitamins”.

“This is the position taken by most of the authorities in the vitamin field. Thiamine as thiamine will meet the body’s needs for this vitamin whether it is the synthetic variety or if it comes as a part of a food like a whole‑grain breakfast food. The natural food, of course, may contain the unknown factors that are missing from a specific mixture of vitamins, and therefore, be superior to this extent.”

(Dr. Cowgill was not aware of the fact that natural thiamine can not be separated from B4, the vitamin that prevents some kinds of heart disease.[8] Therefore, it is impossible to compare natural thiamine with synthetic thiamine. He is comparing the synthetic B1 to a pro­duct purely hypothetical that is not known to science, not available for tests.)

We also obtained the opinion of Dr. S. Ansbacher, U. S. Vitamin Corporation, New York: “There is no difference whatsoever in the physiological activity of vitamins from natural sources and the ones made synthetically.”

(Dr. Ansbacher here differs from a book his own firm published, “Vitamin and Mineral Therapy,” by H. E. Dubin and Casimir Funk, 1936, (Dr. Funk was the discoverer of Vitamin B and the man who invented the word “vitamin.”), in which is the comment: “Synthetic Vitamins: These are highly inferior to vitamins from natural sources, also, the synthetic product is well known to be far more toxic.” Page 65)

Dr. Funk’s opinion is significantly different from that of Dr. Ansbacher, present Research Director of the company. Why is it that none of these men seem able to refer to any concrete reason for their present opinions? Could it be that the profits involved in the sale of synthetic foods and drugs are so great that there is a constant campaign on to cover up the facts?

In the September 1948 issue of “Reader’s Digest” is an article by Paul de Kruff, “Harry Steenbock Trapped the Sun,” that appears to be for the express purpose of reviving the reputation of Steenbock and Viosterol the synthetic and poisonous form of Vitamin D. Aside from the dangerous nature of Steenbock’s vitamin, its promotion by the Wisconsin Alumni Research Foundation was an unconscionable racket. its nature is well exposed in the appended reprint from “This Month,” June 1945…

Viosterol is still on the market. It will still poison your child if YOU do not watch out. Your doctor has not yet been informed by his medical society, (if he is a member of the A. M. A.), that they made a mistake in approving it as real Vitamin D, although all vitamin authorities, including Steenbock himself, who first published the fact, knows that Viosterol is NOT Vitamin D. [9]

The same issue of “Reader’s Digest” carries an article on the nickel‑cadmium storage battery, a
common article in Europe for the last 40 years. it is completely unknown in this country.
WHY? Simply because the American makers of lead storage batteries have succeeded in
keeping out any knowledge of this battery from all American territories, and have stopped any
production in this country by hook or crook, (as the article tells it, by acquiring control of the
European concerns), all to protect their racket of selling a short‑lived battery to their customers text books ignore the cadmium battery.

In Canada the adulteration of white flour with synthetic vitamins is a criminal offense. In this country it is an approved practice, and the makers of synthetic vitamins reap a fat harvest for their contribution to the advertising propaganda of the flour millers. The real vitamins are removed to keep insects and molds out of the flour. Synthetic vitamins are added to fool the public, which knows that white flour without vitamins is unfit to eat. The fact that insects and molds still can not live in the flour any better than before the synthetic vitamins were added is not mentioned. Neither is the fact mentioned that test animals fed enriched” diets, (“enriched” with synthetic imitations of natural vitamins), DIE SOONER than control animals fed the deficient diets. Proof that synthetic vitamins are worse than none as food fortifiers, [10], proof that they are put into foods to defraud the buyers, cheat him out of his health and life, as well as his money.

This situation cannot be an accident. It must be a carefully planned conspiracy, with varying degrees of guilt for all the pseudo‑ scientists who have varying degrees of knowledge of the real situation, and who do not dare to expose the truth.

Food & Drug Inspectors and Officials are as helpless to combat this overwhelming influence as they would be to stop the sale of bootleg whiskey during prohibition days. To keep their jobs they have to keep one eye shut.

Dr. Harvey W. Wiley, the first head of the Federal Food & Drug Department tried to stop the use of synthetic sugar, known as glucose of com sugar, in preserved fruits and canned goods. He felt that it was a fraudulent practice to load up such foods with synthetic materials of unknown effect on the human body. Further, people eat sugar as a sweetener, and the synthetic sugar was far less sweet than cane sugar, and would have to eat much more to get the same taste when added to preserves, etc. Dr. Wiley lost out in his desire to even get the label warning on containers that the product carried synthetic sugar, in fact, lost his job because he tried to protect the public.

Only this year have supporting tests confirmed Dr. Wiley’s fears. On May 10, 1948, the University of Pennsylvania released the news to the Associated Press that they had found that the feeding of glucose to test animals caused diabetes. (Dr. Francis D. W. Lukens and Dr.
F. Curtis Dohan.)

Dr. Wiley thought that glucose was a possible cause of diabetes, but had no way to prove it. He felt that the makers of glucose should not be permitted to experiment on the whole population of the United States to find out.

It is the use of glucose in candy, soft drinks, bakery goods, ice cream, canned fruit etc., the low price of which enables their users to undersell all competitors who may try to use better sugars, and put them out of business. It is a clear case of where the public SHOULD be protected by a law, but, as Dr. Wiley said when he was forced to leave his job                       “thus the very law which the Supreme Court has said was enacted chiefly to protect the public health has
been turned into a measure to threaten public health and to defraud the purchaser of flour.

When you add up the industries that depend upon their foisting of synthetics as foods alone, (not considering drugs), you will find you have a list of the biggest in the country. Naturally, they are watching all loopholes where their rackets might start to crack. It is probably impossible for any research worker operating under the auspices of a university or in a government laboratory to be free from their indirect influence, Such items as have been quoted here are leaks that have commonly been quickly suppressed. No further work is done on these important questions. If a book like Dr. Daniel W. Quigley’s, “The National Malnutrition which exposes these food racketeers, gets into public libraries, these influences get it off the shelves. This happened at Rochester, New York, where twelve of the Quigley books were donated by request, for the library and its branches. Later, when it was found that the books had been taken off the circulating list, the librarian admitted that no book inimical to local, industries could remain on the library shelves. Later, that same librarian was Written up in the local paper as a “Champion of FREE libraries where no outside influence could alter the nature of the “free speech” of the library. (Rochester Democrat & Chronicle, November 21, 1944.) Was this a deliberate attempt to nullify a truth by circulating a lie? Or, maybe just a coincidence.

The Food & Drug Administration, and the Federal Trade Commission, instead of getting the facts in this situation and protecting the public against these dangerous imitations of natural foods, are bending their energies it seems to cover up for the racketeers.

We cannot find a single instance of where a maker of synthetic imitation vitamins has been prosecuted by the Food & Drug Administration for improper claims on his labels or advertising. But many makers of NATURAL products have been prosecuted for making claims IDENTICAL to what the makers of synthetic products are constantly and continually promoting. WHY THE SELECTION OF THE MAKERS OF NATURAL PRODUCTS FOR PERSECUTION? In one case in which we have the transcript at hand, the prosecuting attorney was successful in getting the testimony of a key witness REVERSED in the process of printing the record, which the Court of Appeals was able to use to support their argument to uphold the original judgment Without this help, it is hard to see where the original verdict could have been sustained, obtained as it was by obvious fraud, where Government “experts” declared no, vitamin deficiency could create either a degenerative, infectious, or a functional disease.

The Federal Trade Commission has issued orders and interpretations to makers of natural vitamins to “cease and desist” stating that a synthetic vitamin is in any way inferior to a natural.

Pages could be filled with examples of misuse of authority of this kind, where special business interests are being protected by police activity. If one asks the question, “Why do they prosecute one concern for a violation, and then let far bigger ones continue to use the pro­hibited advertising‑‑if it is wrong for one to make a statement why is it not wrong for another? The answer you get is “action can only be taken where a complaint is made, no one has filed a complaint against these concerns.”

If a police authority can stop a murderer only after someone files a complaint, lets get busy and start filing complaints. For a lot of people are being murdered, slowly maybe in most cases, but none the less surely, by food racketeers, who are constantly finding ways to make a poor product worse, and sell it for less, thereby driving better ones off the market. On top of this, they are using the police power to stop the maker of better products from telling the truth on his label as to the difference.

Just WHY should the TRUTH be subservient to the OPINIONS of hired crooks who sell their reputations as EXPERT WITNESSES?

Can you imagine a better way to protect racketeers under the Federal laws? Or a better way for them to discredit their competitors?  ”[12]

References (These references are listed the same way that Royal Lee listed them)

[1]      Crofton, W. M.: AN OUTLINE OF ENDOCRINOLOGY. Wm. Wood and Company, New York,
Second Edition, 1929.

]2] Lee, R. and W. A. Hanson: PROTOMORPHOLOGY. Lee Foundation for Nutritional Research,, Milwaukee, Wisconsin, 1947.

[3] Young, E. G. and R. P. Smith: LACTIC ACID: A CORROSIVE POISON. Journal of American Medical Association 125:1179‑1181) 1944.

[4] Harrow and Sherman: THE CHEMISTRY OF THE HORMONES. Williams & Wilkins, Baltimore, Maryland, page 122, 1934.

[5] Dyson: THE CHEMISTRY OF CHEMOTHERAPY. The Chemical Publishing Company, Brooklyn, New York, page 66.

[6] THE RELATIVE ACTIVITY OF NATURAL AND SYNTHETIC VITAMIN E. Nutrition Reviews 5:251‑253,1947.

[7] Bauer, J. M. and R. H. Freyberg: VITAMIN D INTOXICATION WITH METASTATIC CALCIFICATION. Journal of American Medical Association 130:1208‑1215,1946.

[8] Stepp, W., Kuhnau, J. and H. Schroeder: THE VITAMINS AND THEIR CLINICAL APPLICATIONS. English translation published by The Vitamin Products Company, Milwaukee, Wisconsin, page 24, 1938

[9] Steenbock, H., Kletzein, S. N. F. and J. G. Halpin: THE REACTION OF THE CHICKEN TO IRRADIATED ERGOSTEROL AND IRRADIATED YEAST AS CONTRASTED WITH THE NATURAL VITAMIN D OF FISH LIVER OIL. Journal of Biological Chemistry 97:249,1932.

DeSanctis, A. and J. D. Craig: A FIVE‑YEAR CLINICAL STUDY OF THE PROPHYLACTIC VALUE OFANTIRACHITIC AGENTS. New York journal of Medicine 34:712‑714,1934.

[10] Morgan, Agnes Fay: THE EFFECT OF IMBALANCE IN THE “FILTRATE FRACTION” OF THE VITAMIN B COMPLEX IN DOGS. Science page 261, March 14,1941.

[11] Wiley, H. W.: THE HISTORY OF A CRIME AGAINST THE PURE FOOD LAW. Published by himself, page 391, 1929.

[12] Lee R.  How and Why Synthetic Poisons are Sold as Imitations of Natural Foods and Drugs.  Lee Foundation for Nutritional Research, Milwaukee, 1948

The above is an excerpt written by Royal Lee and from the book, Serious Nutrition: Incorporating Clinically Effective Nutrition Into Your Practice.

Royal Lee, in addition:

The late Dr. Royal Lee knew that food vitamins were superior to synthetic ones.

For another example, Dr. Royal Lee felt that food vitamin C was superior to ascorbic acid. “Dr. Lee felt it was not honest to use the name ‘vitamin C’ for ascorbic acid. That term ‘should be reserved for the vitamin C COMPLEX'” [DeCava, J. The Lee Philosophy-Part II. Nutrition News and Views 2003;7(1):1-6].

Why then, according to the ingredients listed in a recent catalog, would a supplement company that Dr. Lee originally founded currently include ascorbic acid, inorganic mineral salts, and/or other isolated nutrients in the majority of its products?

Dr. Lee, like the late Dr. Bernard Jensen [Jensen B. Chemistry of Man. Bernard Jensen, Escondido (CA), 1983], was also opposed to the use of other isolated, synthetic, nutrients [DeCava, J. The Lee Philosophy-Part II. Nutrition News and Views 2003;7(1):1-6].

As shown earlier, Dr Lee specifically wrote, “In fact, the Food & Drug laws seem to be suspended where synthetic imitations of good foods are concerned, and actually perverted to prosecute makers and sellers of real products. The synthetic product is always a simple chemical substance, while the natural is a complex mixture of related and similar materials. Pure natural Vitamin E was found three times as potent as pure synthetic Vitamin E. Of course the poisonous nature of the synthetic Vitamin D is well established. WHY DO NOT THE PEOPLE AND MEDICAL MEN KNOW THESE FACTS? Is it because the commercial promoters of cheap imitation food and drug products spend enough money to stop the leaking out of information?” [Lee R. How and Why Synthetic Poisons Sold as Imitations of Natural Foods and Drugs? 1948].

All products distributed by Doctors’ Research, Inc. are nutritional and are not intended for the treatment or prevention of any medical condition.

Diabetes: Types I and II

In the United States, the incidence of diabetes in adults rose by 33% from 1990 to 1998 [1] and still appears to be on the rise.  Obesity is considered one of the major risk factors for diabetes [2-4], but that may be more due to dietary choices, including quantity of food, and lack of exercise than weight itself.  Proper food nutrition can play an important role in this disorder.

Diabetes mellitus is a “syndrome characterized by hyperglycemia resulting from absolute or relative impairment in insulin secretion and/or insulin action…Patients with type I diabetes mellitus (DM), also known as insulin-dependent or juvenile onset diabetes, may develop diabetic ketoacidosis.  Patients with type II DM, also known as non-insulin-dependent DM may develop non-ketotic hyperglyemic-hyperosmolar coma.  Common late microvascular complications include retinopathy, nephropathy, and peripheral and autonomic neuropathies.  Macrovascular complications include atherosclerotic coronary and peripheral arterial disease” [3].  Type I DM typically occurs in those less than 30 years of age, while type II usually occurs in those above age 30.  Type I is normally due to low insulin production due to the destruction of pancreatic beta cells [4].  Type II is normally due to insulin resistance (diminished tissue sensitivity to insulin) and impaired beta cell functioning [4].  Obesity is more common in type II [2,3].  Other types include gestational diabetes, malnutrition-related diabetes mellitus, impaired glucose tolerance, as well as some due to genetics, medications, and hormones [4].  It is estimated that 7,000,000 Americans with type II are undiagnosed [4].

Nutrition can affect those with type of diabetes.  The human brain primarily runs on glucose [5].  Nearly all calories, be they from bananas, steak, or candy bars, are converted by the body into glucose (blood sugar).  If the amount of glucose converted is excessive, this will trigger the body’s need to secrete insulin.  But just because nearly all calories in foods are converted to glucose, does not make all foods equal; some foods take longer to be converted.  Those that take longer to convert are known as foods with a lower glycemic effect, whereas those that convert quickly are known to have a higher glycemic effect.  Those foods with a low enough glycemic effect do not cause the body to need to secrete insulin because they provide glucose at such a rate that it is consumed rather than accumulated.

Excessive glucose causes the accumulation of glycogen in non-insulin dependent tissues [4].  Glycoxidation is “a process that occurs with elevated blood glucose levels.  Another pathway that results in the modification of LDL proteins involves the formation of Amadori products.  An adequate amount of antioxidants from the diet or supplements may help prevent or delay the occurrence of diabetic late syndrome” [6].  The formation of Amadori products is a type of nonenzymatic glycosylation [4], and is reversible.  Price et al have stated, “The Maillard or browning reaction between sugars and proteins leads to the formation of chemical modifications and cross-links in proteins, known as advanced glycation end-products (AGEs).  These products contribute to the age-dependent chemical modification of long lived proteins, and accelerated formation of AGEs during hyperglycemia is implicated in the development of diabetic complications” [7] as “sugars react with amino groups in proteins, lipids, and nucleic acids to produce advanced glycation end products” [8].

Diet and Lifestyle Factors

As glycation end products tend to accumulate as the result of disorders of sugar metabolism such as diabetes, it is generally believed that a diet low in refined carbohydrates is a logical choice for those with diabetes.  Diets naturally high in vitamin C have been shown to result in reduced protein glycation [9].  Though this would not stop all glycation end products from forming and accumulating, it may reduce their formation and possibly delay the onset of some of the complications associated with diabetes.

The average adult who develops diabetes consumes less fruits and vegetables than those who do not [10].  Interestingly, one study found that dietary carotenoid intake was inversely related to fasting plasma glucose concentrations; that plasma beta-carotene concentrations were inversely associated with insulin resistance; and that dietary lycopene was directly related to baseline serum concentrations of nonesterified fatty acids [11].  Dietary carotenoids primarily come from vegetables and to a lesser degree from fruits.  It should be noted that a large study that tested isolated betacarotene found that it did not help prevent diabetes [12].

Reducing weight, increasing consumption of fiber, exercise, and reducing the intake of saturated fats also reduce the risk of developing diabetes, even for those with impaired glucose tolerance [13].  Consumption of whole grains is also associated with reduced risk of developing diabetes [14]; this could be due to the natural B vitamins, lower glycemic effect, or simply the fiber of whole grains compared to refined grains.  Similarly, nut consumption has been found to be inversely associated with the risk of type II DM [15].

One risk factor for type I DM is early exposure to cow’s milk, especially if a sibling has sensitivity to milk [16,17].  It has been reported that wheat, soy, and perhaps other foods can provoke pancreatic beta cell destruction through immunological mechanisms in some [18].  In type I diabetes mellitus, hyperglycemia results in the intracellular accumulation of the sugar alcohol sorbitol by the action of aldose reductase on glucose [19].  Based on this evidence, sorbitol and similar alcohol sugars should probably be avoided.  It has been proposed that insulin dependent diabetes may be started by an immunization from environmental proteins such as a virus with molecular mimicry with the islet cell enzyme glutamic acid dehydrogenase, initiating the process [20].  In the islets, GABA inhibits glucagon secretion.  In susceptible individuals the anti-enzyme glutamic acid dehydrogenase immune response may be sufficient to initiate islet cell autoimmunity and damage.  Autoantibodies to insulin and islet cell cytoplasmic glycolipid antigens result and beta cells are lost.  Officially, type I DM occurs only after destruction of the bulk of the insulin-secreting beta cells.  The entire process usually takes years to complete but is faster in young children than adults.  Quite recently a Finnish study found that enterovirus strains were present in 11 of 12 children considered to be pre-type I diabetic [21].

The probable factors predisposing one towards type II DM include obesity, genetics, poor diet, and hypoglycemia [1,2,10,18].  Furthermore, over-consumption of high glycemic foods is probably the factor that has lead to increases in diabetes throughout the world [2], specifically, items such as refined carbohydrates, sugar, sugar-substitutes, soft drinks, white pasta, white rice, white flour, alcohol, and combinations of those substances.  Lower glycemic foods generally include those high in fats, proteins, fiber, and complex carbohydrates; however those at risk for diabetic nephropathy should at least moderately-restrict proteins [4,18].  Eating frequent small meals can also be helpful in keeping blood glucose levels in more desired ranges [18].

Low intensity exercise, such as walking, has been found to significantly reduce blood-glucose levels in type II DM [22].  Caloric restriction and exercise are among the best ways to reduce insulin resistance [23].  Additionally, “high carbohydrate, high fiber diets increase insulin sensitivity and decrease insulin requirements” [4] while caffeine may decrease it [24].  Thus caffeine itself is not advised for diabetics.

Although alcohol itself does raise blood sugar, one large study found that men who drink alcohol moderately have a lower risk of contracting diabetes compared with those who drink heavily or those who drink very little [26].

Raised plasma nonesterified fatty acids are a risk factor for the deterioration of glucose tolerance from normal to impaired, and from impaired to type II DM.  Circulating concentrations of nonesterified fatty acids are elevated in obesity, Type II diabetes and in uncontrolled Type I diabetes or insulin deficiency [25].

Whether it has to do with increased walking, caloric restriction, increased consumption of wild plants, and/or increased consumption of animal glands, Australian Aborigines who forsake the Western lifestyle for a native one have been able to dramatically reverse complications associated with type II diabetes (18,27).

Beneficial Food Nutrients

Many nutrients have been found to be of benefit to people with diabetes.  B vitamins are involved in the production of energy as well as other metabolic processes [23].  B complex vitamins, potassium, and trace minerals are often recommended for diabetics, particularly for the prevention and reversal of oxidative-dysoxygenative insulin dysfunction [28].  Many food nutrients have been reported to have prevent the accumulation of advanced protein glycation end-products [29], which can be a major problem for diabetics.

Thiamin (vitamin B-1) may be helpful for some with diabetic retinopathy [18].  Benfotiamine, a lipid soluble derivative of thiamin, found in leeks, onions, garlic, and shallots can be helpful for many diabetics.

While niacinamide, which can be found in food, has been shown to be helpful for insulin-dependent diabetics (type I DM), niacin, which seldom exists in any substantial quantity in food [23]), tends to worsen (increase) glucose concentrations for those non-insulin dependent diabetics (type II DM) [18].  Niacinamide can also inhibit glycation.

In non-diabetics, a subclinical deficiency of vitamin B-6 can cause insulin resistance [18].  Both type I and type II DM sometimes have marginal B-6 levels [18].  Vitamin B-6 deficiency has been associated with impairments in gluconeogenesis and abnormal glucose intolerance.  Vitamin B-6 has been recommended to help deal with glycation [30].  Furthermore, it or its derivatives have been shown to have anti-glycation effects [7].

One study found that serum levels of females with type I DM tended to be low in folate and high in homocysteine [31].  Folate is the form found in food, and has less affinity for serum folate-binding proteins than folic acid, the form most commonly found in nutritional supplements [16].  Thus folate may be the preferred from.

It should be noted that it has been shown that up to 2,000 mg per day of metformin (Glucophage) can increase total homocysteine levels and decrease vitamin B-12 and folate levels [32].  Thus it is logical that diabetics on that medication consider taking food vitamin B-12 and food folate.  Furthermore it has been found that methylcobalamin, the type of vitamin B-12 found in food [23], may ameliorate the development of diabetic neuropathy [18].

Increasing plasma vitamin C through dietary means has been suggested as an important way for the public to reduce the prevalence of diabetes mellitus [33].  Diabetics have vitamin C levels 30% (or more) lower than non-diabetics and part of this may be due to increased urinary excretion [18].  Vitamin C containing food has over 15.6 times the ORAC of isolated ascorbic acid [34].  Since food vitamin C has proven antioxidant effects in vivo [35] and isolated ascorbic acid does not [36], it seems reasonable to conclude that food vitamin C both prevents oxidative damage and ‘cleans up’ damage much better than isolated ascorbic acid.

Activated vitamin D is required by the islet cell to be able to secrete insulin normally.  One study found that vitamin D status related directly to the capacity to secrete insulin and inversely to glucose tolerance [37].

A double-blind study found that vitamin E improves endothilial vasodilator function in type 1 diabetics [38].  High vitamin E vegetable oil has been found to have significant anti-glycation effects [19].  Consumption of vitamin C and vitamin E prior to a high fat meal has been found to reduce the production of meal-induced C-reactive protein in diabetics [39].  One study found there is an increase in lipid peroxidation after the correction of diabetic ketoacidosis, and administration of antioxidant vitamins, like vitamin E, during the treatment of diabetic ketoacidosis may be of benefit in minimizing oxidative stress and possibly preventing complications of type II diabetes mellitus [40].  Consumption of vitamin E in foods was recently found to reduce the incidence of type II DM [41].

One study found that 30% of those with type II DM in its study were deficient in zinc, and that supplementation with zinc alone, chromium alone, and zinc with chromium resulted in significant reduction of plasma thiobarbituric acid reactive substances (TBARS) by 13.6%, 13.6%, and 18.2% respectively [42]; no adverse side effects were noted.

Zinc is involved in insulin physiology.  It enhances the magnitude of the binding of insulin to the receptor, but simultaneously inhibits the degradation of insulin by the liver plasma membranes.  Zinc modulates insulin’s actions by stimulating lipogenesis in adipocytes in a synergistic relationship with insulin [43].  Zinc is a cofactor of key enzymes in glucose metabolism [23].  Some feel that insulin resistance may be related to zinc deficiency by impairment of insulin secretion by the pancreas; interference in insulin-receptor binding; decreased insulin-receptor synthesis; and abnormal glucose carrier structure and/or translocation inside the cell [43].  It is unclear if diabetic patients malabsorb zinc or are unable to compensate for the excessive urinary loss [43,44].  It has been speculated that zinc deficiency may account for impaired wound healing, decreased cell-mediated immunity and taste acuity in diabetic subjects [43].  One researcher noted that although many diabetics are low in zinc, supplemental zinc, as typically used in mineral salt forms, does not apparently absorb well enough to raise zinc levels [44].  On the other hand, high zinc yeast has been found to be better absorbed than non-yeast forms [45].

Vanadium is found in skim milk, vegetable oils, many vegetables, grains and cereals.  Mushrooms, parsley, dill and black pepper are particularly rich in vanadium [46].  Daily consumption in humans ranges from 10 µg to 2 mg [47].  One human study involving 11 type II diabetics found that vanadium significantly improved glycemic control, and fasting plasma glucose was reduced from 194 to 155 mg/dl, hemoglobin A1C from 8.1 to 7.6%, and fructosamine from 348 to 293 µmol/l and reduced endogenous glucose production by approximately 20%, which correlated with a reduction in fasting plasma glucose [48].  It has been reported that organic forms of vanadium are safer, more absorbable and able to deliver a therapeutic effect up to 50% greater than inorganic forms [47].

A French study found that diabetics had significantly lower levels of selenium than controls [49]. Reduced selenium concentrations in the red blood cells of the diabetic patients have been found to contribute to impaired hemorrheology [50].  One study found that high yeast selenium was 123.01 more effective than selenium methionine in preventing nonenzymatic glycation in diabetics [29].  Glycation end-products tend to also accumulate in the brains of those who develop Alzheimer’s or similar forms of dementia [51].  This same study found that high selenium yeast was more effective than ascorbic acid, niacinamide, carnosine, tocopherol, and pyridoxal [29].  Selenium “is the co-factor of glutathione peroxidse (Se GSHpx).  Low Se GSHpx is activity, observed in diabetic patients, is associated with thrombosis and cardiovascular complications” [52].

Hypophosphatemia (low phosphorus levels) is clinically associated with diabetes mellitus [23]; “Excessive amounts of phosphorus can also be lost in the urine of uncontrolled diabetics who have polyuria and acidosis” even if plasma phosphorus appears to be normal [23].  Vegetables and fruits are high in phosphorus and thus consumption of them would appear to be a logical way to improve phosphorus levels.

Some research has suggested that lithium can be helpful for diabetics [54].  Min Hu, a medical doctor who has looked into this for eight years, reported, “Lithium has some insulin-like effects. Experiments in vivo demonstrate that lithium has little effect on insulin secretion, but does have an effect on reduction of insulin resistance.  Experiments in vitro further demonstrate that lithium has some insulin-like effects, such as lithium’s ability to promote glucose uptake and glycogenesis in adipocytes and in hepatocytes.  1) Lithium inhibits hepatic gluconeogenesis and phosphoenol pyruvate carboxykinase gene expression, which can lower the blood glucose.  2) Lithium has some antioxidative effects, which can enhance insulin action in target cells. 3) Lithium increases DNA replication, polyamine content and insulin secretion by pancreatic beta cells in rats” [55].  Hu, et al. wrote, “restoration of lithium to control levels in the liver and muscle of diabetic animals is associated not only with decreased blood glucose but also with reduced oxidative stress, and consequently with the protection of insulin-secreting pancreatic islet cells” [56].  Caution is advised, however, as lithium can induce diabetes insipitus in some individuals.  “Fortunately, lithium toxicity is both entirely preventable and easily treatable” [57] with flaxseed oil and vitamin E [57].

Chromium and Saccharomyces Cerevisiae

Insufficient dietary intakes of chromium can lead to diabetes [58].  “Chromium is generally accepted as an essential nutrient that potentiates insulin action, and thus influences carbohydrate, lipid, and protein metabolism” [53].  Food chromium is safer than some non-food forms, like chromium picolinate [59].  One study found that yeast chromium was as effective as 8.62 time as much chromium chloride in causing improvement in glucose control [60].  And unlike rock-forms of chromium, Saccharomyces cerevisiae yeast-forms also contains a variety of essential vitamins, minerals, and amino acids [61].

“The biologically active form of chromium, sometimes called glucose tolerance factor or GTF, has been proposed to be a complex of chromium, nicotinic acid, and possibly the amino acids glycine, cysteine, and glutamic acid.  Many attempts have been made to isolate or synthesize the glucose tolerance factor; none have been successful” [53].  Chromium is not naturally found in the body in the commonly supplemented forms such as chromium picolinate or chromium chelate.  Only 1% or less of inorganic chromium is absorbed versus 10-25% of chromium GTF [62].

Scientific research has concluded that “supplementation of well-controlled type 2 diabetics with Cr-enriched yeast is safe and can result in improvements in blood glucose variables and oxidative stress” [63] and that “dietary high Cr yeast supplementation improved glucose tolerance, probably through a decrease in hepatic extraction of insulin” [64].  This type of food chromium really is the best form for supplementation for diabetics.

In Iraq, barley bread is commonly used in the treatment of diabetes because of its ability to modulate the glycemic response to carbohydrate ingestion, and slow weight loss and excessive water consumption.  Animal studies have verified that barley bread does contain significant amounts of food chromium [65], which may account for some of its effectiveness.

Chromium in food has accompanying food factors such as protein chaperones [66,67] which aid in absorption of chromium.  Chromium mineral salts are chemical compounds which are rocks or synthetically produced.  Chromium rocks are poorly absorbed by humans; some are less than 1% absorbed [62].  Chromium picolinate is a human-made substance, apparently created by Gary Evans [68].  Picolinic acid is used in herbicides [69]; furthermore “picolinic acid is an excretory or waste product.  It is not metabolized by or useful to the body” [70].

Saccharomyces cerevisiae is also known as nutritional or baker’s yeast and it holds several unique advantages for diabetics.  Perhaps the first is that it is the most natural medium in which to grow the GTF form of chromium.  Additionally, Saccharomyces cerevisiae has proinsulin-like substances; “the specificity of the yeast processing enzymes is so similar to the proinsulin converting enzymes in the human pancreatic beta-cell that it allows the processing of the mini-proinsulin to insulin” [71].  Saccharomyces cerevisiae also contains a variety of insulin precursors that can be helpful for diabetics [72].  In 1999, the Nobel Prize was awarded for discovering that protein chaperones are necessary for mineral transport into cellular receptors.  Saccharomyces cerevisiae, like other mineral containing foods, naturally contains protein chaperones and other factors that aid in mineral absorption [66,67].  These are lacking in mineral salts.

Saccharomyces cerevisiae is beneficial to humans and can help combat various infections [73], including Candida albicans.It should also be noted, that W. Crook, M.D., who was perhaps the nation’s best known expert on Candida albicans, wrote “yeasty foods don’t encourage candida growth…Eating a yeast-containing food does not make candida organisms multiply” [74].  It should also be noted that nutritional yeast is not the same as brewer’s yeast which is essentially a waste by-product.  Saccharomyces cerevisiae naturally contains vitamins B-1, B-2, B-6, niacinamide (B-3), folate (B-9), and pantothenate (B-5) plus phosphorus, potassium, and a variety of trace minerals.

Rice Bran, Cinnamon, Fenugreek, Gymena, and Other Herbs Substances

Various types of rice bran have been found to help lower glucose levels for people with type I or type II DM [75].  Due to its high fiber and bran content, brown rice may be an ideal food for some with diabetes, and is so used by some in Chinese medicine [73].

Cinnamon Bark Cinnamon cassia has been found to improve fasting blood glucose (FBG) [76]. Another recent study confirmed that natural ground cinnamon in amounts as little as 1 gram per day was effective in reducing fasting serum glucose levels for those with type II diabetes [77].  Cinnamon is considered to be contraindicated during pregnancy [73].  Cinnamon Bark Cinnamon cassia     has been found to improve fasting blood glucose (FBG) [76].  Another cinnamon study noticed FBG improvement with “significant decrease in plasma C-peptide, serum triglyceride, total cholesterol and blood urea nitrogen levels while serum high density lipoprotein (HDL)-cholesterol levels were significantly increased” [78] (HDL is known as “good cholesterol”). “Cinnamon extract regulates glucose transporter and insulin-signaling gene expression… and this regulation could contribute to the potential health benefits of CE” (cinnamon extracts) [79].

Fenugreek Seed Trigonella foenum-graecum has been used as part of a program for blood sugar management.  The PDR states, “Fenugreek reduces blood sugar” [80].  A human study “showed that FBS, TG and VLDL-C decreased significantly (25 %, 30 % and 30.6 % respectively) after taking fenugreek seed soaked in hot water” [81].  An animal study concluded that “fenugreek oil significantly improved blood glucose levels, glucose intolerance, and insulin sensitivity compared to the diabetic group… diabetic rats showed low activities of superoxide dismutase, catalase, glutathione peroxidase, and reduced glutathione content in kidney, which were restored to near normal levels by treatment with fenugreek oil. The increased levels of lipid peroxidation, creatinine, albumin, and urea in diabetic rats decreased significantly in diabetic rats treated with fenugreek oil. Diabetic rats treated with fenugreek oil restored almost a normal architecture of pancreas and kidney. In conclusion, this study reveals the efficacy of fenugreek oil in the amelioration of diabetes, hematological status, and renal toxicity which may be attributed to its immunomodulatory activity and insulin stimulation action along with its antioxidant potential” [82].  A recent study “confirms the anti-hyperglycaemic and anti-dyslipidemic properties of 4-hydroxyisoleucine, an unusual amino acid isolated from Trigonella foenum-graecum seeds, for the first time in a well-characterised model of type II diabetes… significantly (p < 0.05) declined their elevated blood glucose, plasma insulin, triglycerides, total cholesterol, low-density lipoprotein-cholesterol levels and raised their declined plasma high-density lipoprotein-cholesterol level. These results indicate that 4-hydroxyisoleucine exhibits significant potential as an anti-diabetic agent by suppressing progression of type II diabetic states that is suggested by enhancement of insulin sensitivity and glucose uptake in peripheral tissue.” [83].   “Diosgenin present in fenugreek improves glucose metabolism by promoting adipocyte differentiation and inhibiting inflammation in adipose tissues… Trigonella foenum-graecum (fenugreek) can ameliorate hyperglycemia and diabetes” [84].

Goat’s Rue/French Lilac Galega officinalis was the basis for the anti-diabetic medication Metformin (but Metformin is a chemical isolate) [85].  “Guanidine is an active ingredient extracted from Galega officinalis…we observed that guanidine decreased plasma glucose in STZ rats” [86]. “Galega officinalis (galega, Goat’s Rue, French Lilac) is well known for its hypoglycaemic action and has been used as part of a plant mixture in the treatment of diabetes mellitus… During pharmacological investigations … a weight reducing effect of galega was discovered… together with its established hypoglycaemic effects, galega has a novel weight reducing action that, in normal mice, is largely independent of a reduction in food intake. The mechanism of the weight reducing action of galega is unclear but involves loss of body fat” [87].

One study found that guar gum improved long-term glycemic control, postprandial glucose tolerance, and lipid concentrations.  This result suggests that insulin secretion is enhanced by guar gum as reflected by an increased C-peptide [88].  Another study found that type I diabetics taking guar gum had a significant reduction in glucose, hemoglobin A1c, low LDL cholesterol and the LDL cholesterol/HDL ratio [89].

The herb Gymnema sylvestre is sometimes used for diabetics.  It has been shown to reduce sweet taste sensations [90].  However, clinically, some natural health results suggest better success combining it with chromium GTF, vanadium, and food multi-vitamins.  Gymnema Leaf  and Callus  “Gymnema sylvestre is a plant that has found use in the traditional medicine of a number of societies for the management of blood sugar disorders” [91].  “The phyto-constituents of Gymnema sylvestre are used in the treatment of diabetes and obesity” [92].   Various animal studies have found that it has protective effects for the pancreas of diabetics.  It contains substances that researchers have concluded “showed anti-diabetic activities through regenerating beta-cells” [93].

Other researchers have noted, “Indian plants which are most effective and the most commonly studied in relation to diabetes and their complications are: Allium cepa, Allium sativum, Aloe vera, Cajanus cajan, Coccinia indica, Caesalpinia bonducella, Ficus bengalenesis, Gymnema sylvestre, Momordica charantia, Ocimum sanctum, Pterocarpus marsupium, Swertia chirayita, Syzigium cumini, Tinospora cordifolia and Trigonella foenum graecum. Among these we have evaluated M. charantia, Eugenia jambolana, Mucuna pruriens, T. cordifolia, T. foenum graecum, O. sanctum, P. marsupium, Murraya koeingii and Brassica juncea. All plants have shown varying degree of hypoglycemic and anti-hyperglycemic activity” [94].

For those with type I DM, it is possible that anti-viral herbs such as olive leaf and/or wild oregano may have a possible role.  Since the hepatitis C virus can cause or at least contribute to insulin resistance, those same herbs may be of help to some with DM II [95].

Vanadium and Acetyl-l-carnitine

N-Aceytl-L-Cysteine (NAC) (plant source) is a more stable form of the amino acid l-cysteine because it has an acetyl group (CH3CO) attached.  It seems to help with high glucose (HG) levels.  One study stated “Cotreatment with N-acetylcysteine reduced the effect of HG on aromatase gene expression, suggesting that hyperglycemia may perturb biochemical networks because of the elevation of oxidative stress” [96].  Another study concluded, “Our results clearly demonstrate protective effect of NAC is mediated through attenuation of oxidative stress and apoptosis, and suggest therapeutic potential of NAC in attenuation of diabetic neuropathy” [97].  Another diabetic study concluded that the  “antioxidant, N-acetyl-L-cysteine, suppressed glucose-induced osteopontin expression by decreasing ROS concentration” [98] .  “Epidemiological studies have suggested that the levels of advanced glycation end products (AGEs) are enhanced in patients with diabetes mellitus and during the aging process… Our data showed that APP {amyloid precursor protein} was up-regulated by AGEs in vitro and in vivo, and pretreatment of cells with an ROS inhibitor (N-acetyl-L-cysteine) blocked the effects of AGEs” [99].

Vanadium is a mineral believed to support healthy blood levels.  Vanadium “is used in pharmacological quantities to potentiate the effect of insulin” [100].   Studies suggest that vanadium improves fasting blood glucose levels [18].  Vanadium in a ferment “can effectively lower blood glucose levels of diabetic rats” [101].  Vanadium may help with carbohydrate metabolism and seems to have “insulin-like effects” [102].  “Vanadate forms compounds with other biological substances” [103]. “Vanadium has been postulated to play a role in the regulation of (NaK)-ATPase, phosphoryl transferase enzymes, adenylate cyclase, and protein kinases; as an enzyme cofactor in the form of vandyl and in hormone, glucose, lipid, and tooth metabolism” [103]. Vanadium in foods is found in an organic form. Vanadium in Food is safer than non-food forms and also appears to be about 50% more effective [104].

A Note About Synthetics

The American Diabetes Association does not recommend multi-vitamin, multi-mineral formulas for diabetics, though the HCF Nutrition Foundation does [4].  However, neither of them (and they looked at formulas containing synthetics and/or inorganic mineral salts) has actually apparently examined the role of 100% food multi-vitamin, multi-mineral formulas which certain natural health practitioners prefer.

Niacin, which is normally a synthetic form of vitamin B3, is not advised for diabetics because of its induction of insulin resistance [105].  Diabetics, more than most people, really do need to insure that the vitamins and minerals that they take are food and not synthetic.

Conclusion

Many natural health professionals have learned that foods, and high nutrien food supplements, can be of assistance in natural blood sugar control.

With regard to those food nutrients that have been shown to inhibit glycation, like in the case of Down Syndrome and Alzheimer’s [29], an important therapeutic factor to consider is that it would seem wise to administer them as soon as possible after diagnosis of diabetes and regularly through the sufferer’s lifetime when attempting to prevent diabetic complications.

“To be effective in the long term, the nutritional plan must be individually tailored.  Readily available, pre-printed diet sheets…are doomed to eventual failure” [4], which is one of the reasons why natural interventions must be tailored to the individual.  And why individuals with diabetes should seek successful, experienced health professionals.

Most diabetics need to eat more fruits and vegetables and to do more exercise.  And nearly all diabetics will benefit from properly balanced food multi-vitamin, multi-mineral formulas that contain adequate amounts of food chromium and food vanadium as well as additional food nutrients with proven antiglycation properties.  These changes can not only frequently help to improve blood sugar scores, they may also contribute to possible prevention of various complications.

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Some of these studies (or citations) may not conform to peer review standards. Therefore, the results are not conclusive. Professionals can, and often do, come to different conclusions when reviewing scientific data. None of these statements have been reviewed by the FDA. All products distributed by Doctors’ Research, Inc. are nutritional and are not intended for the treatment or prevention of any medical condition