Vitamin C megadosage 

Chemical structure

Vitamin C megadosage is the consumption of vitamin C (ascorbate) in doses well beyond the current Dietary Reference Intake. Proponents state that this dose is similar to the intake of other primates which, like humans, cannot synthesize vitamin C.1 Most animals synthesize vitamin C, reaching much higher cellular concentrations than humans.2 Vitamin C is a recognized antioxidant, which has led to its endorsement by some researchers as a complementary therapy for improving quality of life.3 Vitamin C has been promoted as an effective treatment for the common cold, cancer, polio, and various other illnesses. The evidence for these claims is mixed, although vitamin C is generally regarded as a beneficial antioxidant. There is a strong advocacy movement for such doses of vitamin C, despite a prolonged lack of conclusive medical evidence or large scale, formal trials in the 10 to 200+ grams per day range. Advocates criticize mainstream scientific studies for using doses which are too low, and mainly using oral vitamin C when intravenous vitamin C is preferred.

Contents

Background

Vitamin C is needed in the diet to prevent scurvy, however, from the time it became available in pure form in the 1930s, some physicians have experimented with vitamin C as a treatment for diseases other than scurvy.4 Orthomolecular based megadose recommendations for vitamin C are based mainly on theoretical speculation and observational studies. The speculation arises from the fact that most animals synthesize vitamin C, and achieve much higher cellular concentrations than humans. Irwin Stone coined the term hypoascorbia to describe what he thought was a genetic defect in humans leading to a lower level of vitamin C than other primates. Observational studies began with work by McCormick and Klenner, who used intravenous vitamin C to treat a wide range of illnesses. The highest dose treatments, published clinical results of specific orthomolecular therapy regimes pioneered by Drs. Klenner (repeated IV treatments, 400–700+ (mg/kg)/day56) and Cathcart (oral use until the onset of diarrhea,7 up to ~150 grams ascorbate per day for flu), have remained experimentally unaddressed by conventional medical authorities for decades.

A comprehensive systematic review of vitamin C and the cold found a minor effect (8% in adults, 14% in children) in preventing the cold, but not treating it, and a substantial effect (50%) in preventing the cold in extreme environments.8 Its effect on cancer has been controversial, beginning with a heavily criticized 1976 study which found significantly increased survival among cancer patients treated with intravenous and oral vitamin C.9 Two subsequent studies using only oral ascorbate failed to replicate these findings,10 and vitamin C's use as a cancer treatment was dismissed by mainstream medicine. Recently, it has been revived by several Canadian researchers, who have focused on intravenous vitamin C.11 Their Phase I trial of intravenous vitamin C on cancer patients found no objective response to cancer, although no toxicity was discovered, either.12

Advocates criticize mainstream scientific studies for using doses which are too low, and mainly using oral vitamin C when intravenous vitamin C is preferred.

Dosage

Oral megadose vitamin C as a prevention element is prescribed as part of a comprehensive individualized vitamin regimen. The typical individual's pharmacokinetics of oral solubilized vitamin C requires 5 or more administrations of immediately dissolvable vitamin C for 24 hour coverage as measured by blood levels. Effective time release formulations of vitamin C may allow 24 hour coverage with only 3 oral administrations. Typical daily orthomolecular doses of oral vitamin C for preventative purposes range 5 - 25 grams of ascorbate per day in healthy adults.citation needed Less than 2 grams per day is not considered a principled amount for orthomolecular "megadose" use in healthy people. Linus Pauling's retrospective analyses of several earlier vitamin C studies identified certain subgroups, which involved physical or cold stress, as statistically benefiting from even one gram per day against common respiratory illnesses, but this amount is not considered optimal or even a megadosed daily usage by advocates.citation needed

Oral megadose vitamin C as an oral treatment element for infections and toxic exposures, with a comprehensive individualized or naturopathic regimen, is considered to require both a higher frequency and much greater quantity for effectiveness. Typical oral treatment frequencies with vitamin C range 15 minutes to 2 hours, the more frequent dosing considered more effective and tighter, more easy to optimize, especially during the first few hours of administration. Less frequent administrations during illness, every hour or two, reflect convenience of administration. Time release oral formulations are used for longer periods between doses such as during sleep. Pauling's recommendation of 1-2 grams of ascorbate per hour at the first sign or tickle of a cold is considered a minimal principled effort by advocates. Cathcart's "bowel tolerance" regimen, front loaded for higher frequency and amounts during the first several hours, is considered by advocates the most effective and the maximum practical oral use of vitamin C.citation needed

The Vitamin C Foundation recommends an initial usage of up to 8 grams of vitamin C every 20–30 minutes13 in order to show an effect on the symptoms of a cold infection that is in progress. Equally importantly, the plasma half life of high dose ascorbate is approximately 30 minutes, which implies that most high dose studies have been methodologically defective and would be expected to show a minimum benefit. Clinical studies of divided dose supplementation, predicted on pharmacological grounds to be effective, have only rarely been reported in the literature. Essentially all the claims for high dose vitamin C remain to be scientifically refuted.

Conditions

Common cold

At least 29 controlled clinical trials (many double-blind and placebo-controlled) involving a total of over 11,000 participants have been conducted into vitamin C and the common cold. In several of the largest studies, no effect on common cold incidence is observed, indicating to many scientists that vitamin C has no preventive effects in normally nourished subjects.14 However, other trials claim that vitamin C reduces the duration and severity of colds but not the frequency.1515 16

Heart disease

Vitamin C is the main component of the three ingredients in Linus Pauling's patented but unvalidated preventive cure for lipoprotein(a), which 17 related heart disease, the other two being the amino acid lysine and niacin (a form of Vitamin B3). Lp(a) as an atherosclerotic, evolutionary substitute for ascorbate18 is still discussed as a hypothesis by mainstream medical science19 and the Rath-Pauling related protocols20 have not been rigorously tested, nor have they been evaluated by the FDA (because no one has submitted a drug approval application).

Cancer

In 1976 Linus Pauling and Ewan Cameron published a trial of 100 patients treated with intravenous vitamin C for which showed significantly increased lifespans.9 Two large, placebo-controlled trials of only oral vitamin C in 1979 and 19852122 did not find a positive effect of vitamin C in cancer patients. A recent in vitro study found that low levels of vitamin C inhibited tumor growth, but high levels increased tumor growth.23

In 2005 in vitro (test tube) research funded by the National Institutes of Health indicated that vitamin C administered in pharmacological concentrations (i.e. intravenous) was preferentially toxic to several strains of cancer cells. The authors noted: "These findings give plausibility to intravenous ascorbic acid in cancer treatment, and have unexpected implications for treatment of infections where H2O2 may be beneficial."11 In 2006 the Canadian Medical Association Journal published a case study of three individuals that demonstrated that intravenous vitamin C might subdue advanced-stage cancer, though the authors concede that spontaneous remissions have been known to occur.24

In 2007, a Phase I trial of intravenous vitamin C on cancer patients was announced. The recently published trial of intravenous vitamin C on cancer patients found no objective response to cancer, although no toxicity was discovered, either.12 The primary purpose of this study was to evaluate the safety and tolerability of vitamin C (ascorbic acid) given by injection into the vein. (A Phase I trial assesses only the safety and tolerability of a treatment, not its efficacy.)

In September 2007 a study funded by the NIH at John Hopkins University found that Vitamin C prevents the growth of cancer cells in an animal model, supposedly by the elimination of the HIF-1 (hypoxia-induced factor) protein, which is necessary for cancer growth in oxygen starved environments.25 The authors, however, noted that this study was very preliminary and people "should not rush out and buy bulk supplies of antioxidants as a means of cancer prevention."

A pilot study of intravenous vitamin C on cancer patients was conducted in 2005.26

In 2008 researchers at the National Institute of Diabetes and Digestive and Kidney Diseases in Bethesda, Maryland, gave vitamin C intravenously to mice with human derived cancers and found that it slowed tumor growth by up to 53%. By injecting into the bloodstream it is possible to get much larger amounts of the vitamin to a tumor than is possible with oral supplements. The Cancer Treatment Centers of America (CTCA) in Zion, Illinois, is currently (2008) testing the safety of intravenous vitamin C in late-stage cancer patients for whom there is no other treatment option. 27

Vitamin C supplementation may interfere with effective cancer chemotherapy. A 2008 study from Memorial Sloan-Kettering Cancer Center found that vitamin C was taken up by cancer cells and protected the cells from chemotherapy drugs, raising the possibility that vitamin C might impair the effectiveness of chemotherapy.2829

Treatment of phencyclidine psychosis

Large dosages of vitamin C can be used in the acute treatment of phencyclidine psychosis, It operates as a secondary rather than primary treatment. Usually, 1000-2000 mg. of vitamin C are given intravenously over the course of 5-10 minutes. It is given in combination with a DA-2 antagonist such as haloperidol or risperidone. The antagonist is given intramuscularly and not combined with vitamin C. The vitamin acts synergistically with phencyclidine or its metabolites. 30

Lifespan

A 10-year study from UCLA showed that in a population of more than 11,000 US adults aged 25-74, men who took 800 mg of vitamin C daily lived about six years longer than men who took only 60 mg of vitamin C daily. 31 Nevertheless, this study has been challenged on the basis that the age structure of the group taking vitamin C was different from that of the men who did not, thus creating a misleading result. 32 The authors of this second, seemingly contradictory, study, taking into account details such as overall food consumption, found no evidence of such a protective effect.

Possible adverse effects

While being harmless in most typical quantities, as with all substances to which the human body is exposed, vitamin C can still cause harm under certain conditions. In the medical community, these are known as contraindications.

Side-effects

Although vitamin C can be well tolerated at doses well above the RDA recommendations, megadosing may cause side effects such as stomach upset and laxative effects such as diarrhea. The dose at which these effects may occur varies with the individual and health condition.

Chance of overdose

As discussed previously, vitamin C generally exhibits low toxicity. The LD50 (the dose that will kill 50% of a population) is generally accepted to be 11900 milligrams per kilogram in rat populations.40 Vitamin C proponent Dr. Robert Cathcart M.D. reports that he has used intravenous doses of 60 grams, with simultaneous oral doses of unspecified amount, with no adverse effects.7

Conflicts with prescription drugs

Pharmaceuticals designed to reduce stomach acid, such as the proton pump inhibitors (PPIs), are among the most widely-sold drugs in the world. One PPI, omeprazole (Prilosec), has been found to lower the bioavailability of vitamin C by 12%, independent of dietary intake. The probable mechanism of vitamin C reduction, intragastric pH elevated into alkalinity, would apply to all other PPI drugs, though not necessarily to doses of PPIs low enough to keep the stomach slightly acidic.41

Potential harmful effects

Genetic deficiency and broad spectrum hypotheses

Since its discovery vitamin C has been considered almost a universal panaceacitation needed by some, although this led to suspicions of it being overhyped by others.57

Humans and higher primates, as well as guinea pigs and small number of other animal species, carry a mutated and ineffective form of the enzyme L-gulonolactone oxidase, the fourth and last step in the ascorbate-producing machinery. Cosmic rays or a retrovirus could have caused this mutation, about 40 to 25 million years ago (in the case of anthropoids lineage). The three surviving enzymes continue to produce the precursors to vitamin C but the process is incomplete and the body then disassembles them.

It is agreed by most researchers, proponents and critics altogether, that the amounts of vitamin C consumed by our common anthropoid ancestor in its normal habitat (African rainforests) was amply sufficient to prevent death from scurvy and did not limit its ability to reproduce: i.e., it was an evolutionarily feasible change. Bourne58 (quoted in Stone59), Pauling1 and, recently, Milton60, showed that these amounts were likely 10 to 20 times higher than what modern humans consume when eating cultivated species, as opposed to the less palatable vitamin-C-rich plant species growing in rainforests.

Linus Pauling's popular and influential book How to Live Longer and Feel Better, first published in 1986, advocated very high doses of vitamin C.

In the 1960s, the Nobel-Prize-winning chemist Linus Pauling, after contact with Irwin Stone, began actively promoting vitamin C as a means to greatly improve human health and resistance to disease. His book How to Live Longer and Feel Better was a bestseller and advocated taking more than 10,000 milligrams per day orally, thus approaching the amounts released by the liver directly into the circulation in other mammals: an adult goat, a typical example of a vitamin-C-producing animal, will manufacture more than 13,000 mg of vitamin C per day in normal health and as much as 100,000 mg daily when faced with life-threatening disease, trauma, or stress.61 Pauling's book sold widely and many advocates today see its influence as the reason there was a marked downward trend in US heart disease from the early 1980s onwards.citation needed

Stone's work also informed the practise of Dr. Robert Cathcart, in the 1970s and 1980s. Cathcart developed the concept of bowel tolerance, the use until the onset of diarrhea, followed by tapering of dose. He found that seriously ill people could often tolerate levels of tens of grams per day before their bowel tolerance limit is reached.

Matthias Rath is a controversial German physician who once worked with Pauling and published in the National Academy of Sciences.6263 He is an active proponent and publicist for high dose vitamin C. Pauling's and Rath's extended theory 64 states that deaths from scurvy in humans during the ice age, when vitamin C was scarce, selected for individuals who could repair arteries with a layer of cholesterol, provided by lipoprotein(a), a lipoprotein found in vitamin C-deficient species (higher primates and guinea pigs). Pauling and Rath theorised that, although eventually harmful, lipoprotein deposition on artery walls was beneficial to the Human species and a "surrogate for ascorbate" in that it kept individuals alive until access to vitamin C allowed arterial damage to be repaired. Atherosclerosis is thus a vitamin-C-deficiency disease.

Based on another study by Pauling and colleagues published in the National Academy of Sciences65and other studies,666768 Rath argued publicly that high doses of vitamin C can be effectively used against viral epidemics such as HIV,69 SARS and bird flu.7071

It has been suggested by some advocates that vitamin C is really a food group in its own right, like carbohydrates or protein, and should not be seen as a pharmaceutical or vitamin at all. {Irwin Stone: "The Healing Factor"}

Regulation of vitamin C

Regulation

There are regulations in most countries which limit the claims on the treatment of disease that can be placed on food, drug, and nutrient product labels. Regulations include:

Advocacy arguments

Vitamin C advocates argue that there is a large body of scientific evidence that the vitamin has a wide range of health and therapeutic benefits but which they claim have been ignored. They claim the following factors affect the marketing and distribution of vitamin C, and the dissemination of information concerning the nutrient 73:

See also

Food portal

Further reading

Books

References

  1. ^ a b Pauling L (1970). "Evolution and the need for ascorbic acid". Proc. Natl. Acad. Sci. U.S.A. 67 (4): 1643–8. PMID 5275366. 
  2. ^ Stone, Irwin. Homo sapiens ascorbicus, a biochemically corrected robust human mutant. Med. Hypotheses 5: 711-722, 1979. Online Mendelian Inheritance in Man.
  3. ^ Yeom CH, Jung GC, Song KJ (2007). "Changes of terminal cancer patients' health-related quality of life after high dose vitamin C administration". J. Korean Med. Sci. 22 (1): 7–11. PMID 17297243. ".
  4. ^ "Vitamin C (Ascorbic Acid)". University of Maryland Medical Center (April 2002). Retrieved on 2007-02-19.
  5. ^ Frederick Robert Klenner. "Significance of High Daily Intake of Ascorbic Acid in Preventive Medicine". AscorbateWeb. Retrieved on 2007-02-19.
  6. ^ Frederick R. Klenner. "Observations On the Dose and Administration of Ascorbic Acid When Employed Beyond the Range of A Vitamin In Human Pathology". AscorbateWeb. Retrieved on 2007-02-19.
  7. ^ a b ROBERT F. CATHCART III (1996). "Preparation of Sodium Ascorbate for IV and IM Use". orthomed.com. Retrieved on 2007-02-21.
  8. ^ Douglas RM, Hemilä H (2005). "Vitamin C for Preventing and Treating the Common Cold". PLoS Medicine 2 (6): e168. doi:10.1371/journal.pmed.0020168. 
  9. ^ a b Cameron E, Pauling L (1976) Supplemental Ascorbate in the Supportive Treatment of Cancer: Prolongation of Survival Times in Terminal Human Cancer
  10. ^ 1979 study, 1985 study
  11. ^ a b Chen Q, Espey MG, Krishna MC, et al (September 2005). "Pharmacologic ascorbic acid concentrations selectively kill cancer cells: action as a pro-drug to deliver hydrogen peroxide to tissues". Proc. Natl. Acad. Sci. U.S.A. 102 (38): 13604–9. doi:10.1073/pnas.0506390102. PMID 16157892. PMC: 1224653, http://www.pnas.org/cgi/pmidlookup?view=long&pmid=16157892. 
  12. ^ a b Hoffer LJ, Levine M, Assouline S, et al (June 2008). "Phase I clinical trial of i.v. ascorbic acid in advanced malignancy". Ann. Oncol.. doi:10.1093/annonc/mdn377. PMID 18544557. 
  13. ^ "SUREFIRE CURES FOR THE COMMON COLD OR THE FLU!". The Vitamin C Foundation. Retrieved on 2007-02-19.
  14. ^ [1] Supplement Watch
  15. ^ a b H. Hemilia (1996). "Does Vitamin C Alleviate the Symptoms of the Common Cold?". Scand J Infect Dis 26 (1). 
  16. ^ Douglas RM, Hemilä H (2005). "Vitamin C for Preventing and Treating the Common Cold". PLoS Medicine 2 (6): e168. doi:10.1371/journal.pmed.0020168. 
  17. ^ Rath MW, Pauling LC. U.S. Patent 5,278,189  Prevention and treatment of occlusive cardiovascular disease with ascorbate and substances that inhibit the binding of lipoprotein(A)]. USPTO. 11 Jan 1994.
  18. ^ Rath M, Linus P. Hypothesis: Lipoprotein (a) is a surrogate for ascorbate. Proc Natl Acad Sci USA. Vol 87, 6204–6207, Aug 1990.
  19. ^ Kniffin CL, McKusick VA, Brennan P. APOLIPOPROTEIN(a); LPA. OMIMTM - Online Mendelian Inheritance in Man, Johns Hopkins University. 1986–2006
  20. ^ Jim English and Hyla Cass. "Vitamin C & Heart Health - Linus Pauling’s Collagen Connection". Vitamin Research Products. Retrieved on 2007-02-19.
  21. ^ Creagan ET, Moertel CG, O'Fallon JR, et al. Failure of high-dose vitamin C therapy to benefit patients with advanced cancer. A controlled trial. N Engl J Med 1979;301:687–90
  22. ^ Moertel CG, Fleming TR, Creagan ET, et al. High-dose vitamin C versus placebo in the treatment of patients with advanced cancer who have had no prior chemotherapy. A randomized double-blind comparison. N Engl J Med 1985;312:137–41
  23. ^ Philips N, Keller T, Holmes C (October 2007). "Reciprocal effects of ascorbate on cancer cell growth and the expression of matrix metalloproteinases and transforming growth factor-beta". Cancer Lett. 256 (1): 49–55. doi:10.1016/j.canlet.2007.05.009. PMID 17602832. 
  24. ^ Sebastian J. Padayatty and others. Vitamin C documented to quell advanced-stage cancer in three cases involving bladder, lung, kidney and lymphoma tumors. Canadian Medical Assn Journal 174: 937–42, 2006
  25. ^ [2]September 2007 - study funded by the NIH at John Hopkins University on the cancer stopping mechanism of Vitamin C
  26. ^ Riordan HD, Casciari JJ, González MJ, et al (December 2005). "A pilot clinical study of continuous intravenous ascorbate in terminal cancer patients". P R Health Sci J 24 (4): 269–76. PMID 16570523. 
  27. ^ Vitamin C jabs may combat cancer New Scientist news service 04 August 2008. Accessed August 2008.
  28. ^ Heaney ML, Gardner JR, Karasavvas N, et al (October 2008). "Vitamin C antagonizes the cytotoxic effects of antineoplastic drugs". Cancer Res. 68 (19): 8031–8. doi:10.1158/0008-5472.CAN-08-1490. PMID 18829561. 
  29. ^ Parker-Pope, Tara (2008-10-01). "Vitamin C May Interfere With Cancer Treatment", New York Times. Retrieved on 3 October 2008. 
  30. ^ Giannini AJ, Loiselle RH, DiMarzio LR, Giannini MC (September 1987). "Augmentation of haloperidol by ascorbic acid in phencyclidine intoxication". The American journal of psychiatry 144 (9): 1207–9. PMID 3631319. 
  31. ^ 'Vitamin C intake and mortality among a sample of the United States population.' Epidemiology. 1992 May;3(3):194-202. Published 1992. Accessed January 4, 2008.
  32. ^ "Vitamin Supplement Use and Mortality". Retrieved on 2008-01-10.
  33. ^ Goodwin JS, Tangum MR (November 1998). "Battling quackery: attitudes about micronutrient supplements in American academic medicine". Arch. Intern. Med. 158 (20): 2187–91. PMID 9818798, http://archinte.ama-assn.org/cgi/pmidlookup?view=long&pmid=9818798. 
  34. ^ Massey LK, Liebman M, Kynast-Gales SA (2005). "Ascorbate increases human oxaluria and kidney stone risk" (PDF). J. Nutr. 135 (7): 1673–7. PMID 15987848, http://jn.nutrition.org/cgi/reprint/135/7/1673.pdf. 
  35. ^ Naidu KA (2003). "Vitamin C in human health and disease is still a mystery? An overview." (PDF). J. Nutr. 2 (7): 7. doi:10.1186/1475-2891-2-7. PMID 14498993, http://www.nutritionj.com/content/pdf/1475-2891-2-7.pdf. 
  36. ^ "Bowel Titration>".
  37. ^ "Dr Dan Rutherfor>".
  38. ^ [Nankivell BJ, Murali KM. Renal failure from vitamin C after transplantation. New England J Med 358(4)e4, Jan 28, 2008], access online
  39. ^ AJ Giannini, AE Slaby. A speculation on oranges, puberty, marriage contracts and frozen foods. M.D.25(5):51-52,1981.
  40. ^ "Safety (MSDS) data for ascorbic acid". Oxford University (October 9, 2005). Retrieved on 2007-02-21.
  41. ^ E. B. HENRY, A. CARSWELL, A. WIRZ, V. FYFFE & K. E. L. MCCOLL (September 2005). "Proton pump inhibitors reduce the bioavailability of dietary vitamin C". Alimentary Pharmacology & Therapeutics. Retrieved on 2007-02-21. "The gastric-juice concentration of vitamin C is reduced in subjects with elevated intragastric pH. This is probably because the vitamin is unstable at non-acidic pH and undergoes irreversible denaturation. After 28 days of 40 mg/day of omeprazole, the mean plasma vitamin C level had fallen by 12.3% (P = 0.04)."
  42. ^ [3] Vitamin C produces gene-damaging compounds Accessed July 2007
  43. ^ Balz Frei, Ph.D. (November , 2001). "Vitamin C Doesn't Cause Cancer!". Oregon State University. Retrieved on 2007-02-21.
  44. ^ [4] Caspase-8 dependent TRAIL-induced apoptosis in cancer cell lines is inhibited by Vitamin C and catalase.
  45. ^ Ian D. Podmore, Helen R. Griffiths, Karl E. Herbert, Nalini Mistry, Pratibha Mistry and Joseph Lunec (9 April 1998). "Vitamin C exhibits pro-oxidant properties". Nature 392: 559. doi:10.1038/33308. 
  46. ^ Balz Frei, Ph.D. (November , 2001). "Vitamin C Doesn't Cause Cancer!". Oregon State University. Retrieved on 2007-02-21.
  47. ^ [5] Too much of a good thing? Large doses of vitamin C linked to atherosclerosis
  48. ^ Hokama S, Toma C, Jahana M, Iwanaga M, Morozumi M, Hatano T, Ogawa Y (2000 Winter). Ascorbate conversion to oxalate in alkaline milieu and Proteus mirabilis culture, PubMed. PMID 11156698. 
  49. ^ Massey LK, Liebman M, Kynast-Gales SA (July 2005). "Ascorbate increases human oxaluria and kidney stone risk". J Nutr 123 (7): 1673. PMID 15987848. 
  50. ^ Stephen Lawson (November , 1999). "What About Vitamin C and Kidney Stones?". The Linus Pauling Institute. Retrieved on 2007-02-21.
  51. ^ acu-cell
  52. ^ Jacob RA, Skala JH, Omaye ST, Turnlund JR. (December 1987). "Effect of varying ascorbic acid intakes on copper absorption and ceruloplasmin levels of young men.". J Nutr. 117 (12): 2109–15. PMID 3694287. 
  53. ^ Finley EB, Cerklewski FL. (April 1983). "Influence of ascorbic acid supplementation on copper status in young adult men.". Am J Clin Nutr. 37 (4): 553–6. PMID 6837490. 
  54. ^ Vitamin C A Home Abortion Remedy?
  55. ^ E.P. Samborskaia, "The Mechanism of Artificial Abortion by Use of Ascorbic Acid," Biulleten Eksperimental’noi Biologii i Meditsiny, Vol 62, 1966, pp96-98. Cited in Irwin Stone, The Healing Factor: Vitamin C Against Disease (New York; Grossent & Dunlap, 1977)
  56. ^ [6]Klenner's "primary and lasting benefits in pregnancy"
  57. ^ Harri Hemilä (January 2006). "Do vitamins C and E affect respiratory infections?" (PDF). University of Helsinki. Retrieved on 2007-02-21.
  58. ^ Bourne G. H. (1949). Vitamin C and immunity. Brit. J. Nutrit., 2: 341-346.
  59. ^ Stone I (1966). "On the genetic etiology of scurvy". Acta geneticae medicae et gemellologiae 15 (4): 345–50. PMID 5971711. 
  60. ^ Milton K (1999). "Nutritional characteristics of wild primate foods: do the diets of our closest living relatives have lessons for us?". Nutrition (Burbank, Los Angeles County, Calif.) 15 (6): 488–98. PMID 10378206. 
  61. ^ Stone, Irwin (July 16, 1978). "Eight Decades of Scurvy. The Case History of a Misleading Dietary Hypothesis". Retrieved on 2007-04-06. "Biochemical research in the 1950’s showed that the lesion in scurvy is the absence of the enzyme, L-Gulonolactone oxidase (GLO) in the human liver (Burns, 1959). This enzyme is the last enzyme in a series of four, which converts blood sugar (glucose) into ascorbate in the mammalian liver. This liver metabolite, ascorbate, is produced in an unstressed goat, for instance, at the rate of about 13,000 mg per day per 150 pounds body weight (Chatterjee, 1973). A mammalian feedback mechanism increases this daily ascorbate production many fold under stress (Subramanian et al., 1973)"
  62. ^ Rath M, Pauling L (1990). "Immunological evidence for the accumulation of lipoprotein(a) in the atherosclerotic lesion of the hypoascorbemic guinea pig". Proc. Natl. Acad. Sci. U.S.A. 87 (23): 9388–90. PMID 2147514. 
  63. ^ Rath M, Pauling L (1990). "Hypothesis: lipoprotein(a) is a surrogate for ascorbate". Proc. Natl. Acad. Sci. U.S.A. 87 (16): 6204–7. PMID 2143582. 
  64. ^ Rath, M., Pauling, L. (1992) A unified theory of human cardiovascular disease leading the way to the abolition of this disease as a cause for human mortality. Journal of Orthomolecular Medicine 7: 5-15.7.
  65. ^ Harakeh S, Jariwalla RJ, Pauling L (1990). "Suppression of human immunodeficiency virus replication by ascorbate in chronically and acutely infected cells". Proc. Natl. Acad. Sci. U.S.A. 87 (18): 7245–9. PMID 1698293. 
  66. ^ Harakeh S, Jariwalla R (1991). "Comparative study of the anti-HIV activities of ascorbate and thiol-containing reducing agents in chronically HIV-infected cells". Am J Clin Nutr 54 (6 Suppl): 1231S–1235S. PMID 1720598. 
  67. ^ Harakeh S, Jariwalla R (1997). "NF-kappa B-independent suppression of HIV expression by ascorbic acid". AIDS Res Hum Retroviruses 13 (3): 235–9. PMID 9115810. 
  68. ^ Harakeh S, Jariwalla R. "Ascorbate effect on cytokine stimulation of HIV production". Nutrition 11 (5 Suppl): 684–7. PMID 8748252. 
  69. ^ "Nigeria: Vitamin C Can Suppress HIV/Aids Virus". all Africa.com (22 May 2006). Retrieved on 2006-06-16.
  70. ^ Sarah Boseley (May 14, 2005). "Discredited doctor's 'cure' for Aids ignites life-and-death struggle in South Africa". The Guardian. Retrieved on 2007-02-21.
  71. ^ Dr. Matthias Rath (2005). "Open letter from Dr. Matthias Rath MD to German Chancellor Merkel". Dr. Rath Health Foundation. Retrieved on 2007-02-21.
  72. ^ "Dietary Supplement Health and Education Act of 1994".
  73. ^ The Politics of Therapeutic Evaluation: The Vitamin C and Cancer Controversy Evelleen Richards, Social Studies of Science, Vol. 18, No. 4 (Nov., 1988), pp. 653-701
  74. ^ Misleading information on the properties of vitamin C PLoS Medicine July 05, 2005

External links