Vitamin C megadosage

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Chemical structure
Chemical structure

Vitamin C megadosage is the consumption of vitamin C in doses which are well beyond the current Dietary Reference Intake. Proponents advocate that this dose is similar to the intake of other primates that cannot synthesize vitamin C,[1] and is required to attain concentrations reached by most other animals, who synthesize vitamin C.[2] High doses have been used in an attempt to obtain specific therapeutic effects.[3][4] There is a strong advocacy movement for such doses of vitamin C, despite a prolonged lack of large scale, formal trials and conclusive medical evidence in the 10 to 200+ grams per day range.[citation needed]

Contents

[edit] Advocacy positions

Orthomolecular based megadose recommendations for vitamin C use, based on pharmacological principles and clinical observations, are several fold. Orthomolecularly recognized physicians have long considered intravenous medical use of buffered vitamin C in the range of 30 - 200+ grams per day, along with concurrent oral use, as fastest and most reliable in substantially ameliorating or even curing serious disease of varying type and severity. Lesser amounts of sodium ascorbate IV/IM have been used for toxins and toxic exposures. Megadose, orally administered vitamin C protocols have been recommended by orthomolecular advocates, both for prevention of illness, and separately, in greater frequency and dosages for treatment of frank illness against viral and bacterial infections, various oxidative and biological toxins, and a mechanism in reversing the development of atherosclerosis. Total vitamin C usage advocated with infectious diseases have typically ranged from about 40 to 300 grams per day in adults depending on severity, administration route(s), and tolerances. Vitamin C is sometimes recommended by advocates concurrently with conventional antibiotics for bacterial diseases.[citation needed]

Oral megadose vitamin C as a prevention element, in a comprehensive individualized vitamin regimen, is considered to require both a minimum frequency and a minimum quantity for effectiveness. 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. 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]

[edit] Advocacy arguments

The advocates argue that the NIH does not take into account individual differences such as age, weight, etc. For example, heavier individuals generally need more vitamin C.[citation needed] They point out the figures represent the amount needed to prevent the acute form of deficiency disease, while subclinical levels of the disease are not even acknowledged. That the amount needed to prevent other diseases is not considered.[citation needed] Most mammals can synthesize their own vitamin C in their liver or kidney, and when they become sick they synthesize much larger amounts[citation needed] -- amounts similar to the "megadoses" suggested by vitamin C advocates for sick humans.[citation needed] The advocates believe that the established RDA is one that will prevent the onset of scurvy and is not necessarily the optimal dosage; this belief contradicts statements made by the United States Department of Agriculture as to the purpose of the RDA. The advocates believe that the recommendations in the RDA is considerably less than the body-weight equivalent of what other mammals synthesize for themselves even when in good health.

[edit] Claimed therapeutic applications of high doses

Vitamin C is needed in the diet to prevent scurvy, however, from the time it became available in pure form in the 1930s, some practitioners experimented with vitamin C as a monomolecular treatment for diseases other than scurvy.[5] Modern clinical megadose Vitamin C use is with individualized, usually at higher than RDA amounts, of other vitamins and minerals as well as other nutrients.

[edit] Common cold

A recent 55-study review[6] found a small positive effect of a vitamin C intake on the common cold at low, brief or single daily doses.

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.[7] However, other trials claim that vitamin C reduces the duration and severity of colds but not the frequency.[8][9] [6]

Controlled trials and clinical experience demonstrate that vitamin C in single doses ranging from 100 mg to 2 grams per day have a relatively small effect in unstressed or nondeficient populations. The duration of colds was reduced by 8% for adults and 14% for children. [6]

[edit] Heart disease

Vitamin C is the main component of the three ingredients in Linus Pauling's patented but unvalidated preventive cure for lipoprotein(a)[10] 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 ascorbate[11] is still discussed as a hypothesis by mainstream medical science[12] and the Rath-Pauling related protocols[13] have not been rigorously tested, nor have they been evaluated by the FDA (because no one has submitted a drug approval application[citation needed]).

[edit] Viral diseases, and poisons

Orthomolecular medicine and a minority of scientific opinion sees vitamin C as being a low cost and safe way to treat viral disease and to deal with a wide range of poisons.

Vitamin C has a growing reputation for being useful in the treatment of colds and flu, owing to its recommendation by prominent biochemist Linus Pauling. In the years since Pauling's popular books about vitamin C, general agreement by medical authorities about larger than RDA amounts of vitamin C in health and medicine has remained elusive. Ascorbate usage in studies of up to several grams per day, however, have been associated with decreased cold duration and severity of symptoms, possibly as a result of an antihistamine effect.[14] The highest dose treatments, published clinical results of specific orthomolecular therapy regimes pioneered by Drs. Klenner (repeated IV treatments, 400–700+ (mg/kg)/day[15][16]) and Cathcart (oral use until the onset of diarrhea,[17] up to ~150 grams ascorbate per day for flu), have remained experimentally unaddressed by conventional medical authorities for decades.

The Vitamin C Foundation recommends an initial usage of up to 8 grams of vitamin C every 20–30 minutes[18] in order to show an effect on the symptoms of a cold infection that is in progress. Most of the studies showing little or no effect employ doses of ascorbate such as 100 mg to 500 mg per day, considered "small" by vitamin C advocates. 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. The clinical effectiveness of large and frequent doses of vitamin C is an open scientific question.

[edit] Cancer

According to the American Cancer Society, there have been no studies that have demonstrated a benefit from supplemental forms of Vitamin C in decreasing cancer risk in humans.[19] Two large, placebo-controlled trials in 1979 and 1985 [20][21] could not show any positive effect of vitamin C in cancer patients. Some in vitro studies have suggested that large doses of Vitamin C may actually encourage growth and proliferation of certain tumor lines.[22]

In 2005 in vitro (test tube) research 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."[23] 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.[4]

In January 2007 the US Food and Drug Administration approved a Phase I clinical trial to investigate what doses of intravenous vitamin C are safe as possible cancer treatments. [24][25] (A Phase I trial assesses only the safety and tolerability of a treatment, not its efficacy.)

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.[26] 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."

[edit] 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. [27] 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. [28] 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.

[edit] 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.

  • A genetic condition that results in inadequate levels of the enzyme glucose-6-phosphate dehydrogenase (G6PD), can cause sufferers to develop hemolytic anemia after ingesting specific oxidizing substances (favism}, such as very large dosages of vitamin C. There are common, inexpensive tests for G6PD deficiency.

[edit] 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.

  • Relatively large doses of vitamin C may cause indigestion, particularly when taken on an empty stomach. This generally occurs at doses larger than 10,000 mg / day, but may occur at much higher doses if the patient is ill.[29]
  • When taken in large doses, vitamin C causes diarrhea. The minimum dose that brings about this laxation effect varies on the individual. This has been called the "bowel tolerance limit". It ranges from 5 to 25 grams per day in healthy individuals to 300 milligrams per day in severely ill patients, such as those with AIDS or cancer[citation needed].
  • It has been suggested that large doses of acidic vitamin C solution (ascorbic acid) swished around the mouth, rather than swallowed directly without a neutral rinse, may erode dentition.[30]
  • A 31-year-old Australian woman who had received a kidney transplant died soon afterward as a result of calcium oxalate deposits that destroyed her new kidney function. Doctors concluded that high-dose vitamin C therapy should be avoided in patients with kidney failure.[31] However, oxalate-induced kidney failure has been reported in people with no apparent kidney problem.[citation needed]

[edit] 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.[32] 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.[17]

[edit] 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.[33]

[edit] Potential harmful effects

  • Some test-tube experiments have interpreted that Vitamin C may have possible adverse effects on decomposition of lipid peroxides[34] in nonviable in vivo quantities and conditions[35] and inhibit caspase-8 dependent apoptosis.[36]In April 1998 the journal Nature reported pro-oxidant effects of excessive doses of vitamin C / ascorbic acid.[37] The effects were noted in test tube experiments and on only two of the 20 markers of free radical damage to DNA. They have not been supported by further evidence from living organisms.[38]
  • In April 2000, University of Southern California researchers reported a thickening of the arteries of the neck in persons taking high vitamin C doses. The scientists found that participants who consumed the most vitamin C from supplements had the greatest increase in atherosclerosis, particularly among smokers.[39]
  • A speculated increased risk of kidney stones may be a side effect of taking vitamin C in larger than normal amounts (more than 1 gram). The potential mechanism of action is through the metabolism of vitamin C to dehydroascorbic acid, which is then metabolized to oxalic acid,[40] a known constituent of kidney stones. However, this oxalate issue is still controversial, with evidence being presented for[41] and against[42] the possibility of this side effect.
  • "Rebound scurvy" is a theoretical, never observed, condition that could occur when daily intake of vitamin C is rapidly reduced from a very large amount to a relatively low amount. Advocates suggest this is an exaggeration of the rebound effect which occurs because ascorbate-dependent enzyme reactions continue for 24–48 hours after intake is lowered, and use up vitamin C which is not being replenished.
  • Some writers[43] have identified a risk of poor copper absorption from high doses of vitamin C. Ceruloplasmin levels seem specifically lowered by high vitamin C intake. In one study, 600 milligrams of vitamin C daily led to lower ceruloplasmin levels similar to those caused by copper deficiency.[44] In another, ceruloplasmin levels were significantly reduced.[45]
  • Some alternative medicine proponents suggest that doses of around 6-10 grams per day of vitamin C can induce an abortion in women under 4 weeks of pregnancy.[46] This is based on evidence that high-dose vitamin C increases estrogen levels that may contribute to abortion in early-stage pregnancy, and that these properties have been demonstrated in laboratory animals.[47]. This theory however is in direct opposition to Dr. Klenner's claim that there were no miscarries in over 300 consecutive pregnant patients who received 3g to 6g per day of Vitamin C[48], whereby Dr. Klenner concluded that failure to use this agent in sufficient amounts in pregnancy borders on malpractice.

[edit] Genetic deficiency and broad spectrum hypotheses

Since its discovery vitamin C has been considered almost a universal panacea[citation needed] by some, although this led to suspicions of it being overhyped by others.[49]

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. Bourne[50] (quoted in Stone[51]), Pauling[1] and, recently, Milton[52], 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.
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.[53] 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.[54][55] He is an active proponent and publicist for high dose vitamin C. Pauling's and Rath's extended theory [56] 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 Sciences[57]and other studies,[58][59][60] Rath argued publicly that high doses of vitamin C can be effectively used against viral epidemics such as HIV,[61] SARS and bird flu.[62][63]

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"}

[edit] Politics of vitamin C

[edit] 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:

  • Claims of therapeutic effect with respect to the treatment of any medical condition or disease are prohibited by the Food and Drug Administration (in the USA, and by the corresponding regulatory agencies in other countries) unless the substance has gone through a well established clinical trial with neutral oversight.
  • In the United States, the following notice is mandatory on food, drug, and nutrient product labels which make health claims: These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.[64]

[edit] 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 [65]:

  • There is some evidence of the applications and efficacy of vitamin C, but governmental agency dose and frequency of intake recommendations have remained relatively fixed. This has led some researchers to challenge the recommendations. In 2003 Steve Hickey and Hilary Roberts of the Manchester Metropolitan University published a fundamental criticism of the approach taken to fix the nutritional requirement of vitamin C. They again argued in 2004 that the RDA which is based on blood plasma and white blood cell saturation data from the National Institutes of Health (NIH) was based on flawed data.[66] According to these authors, the doses required to achieve blood, tissue and body "saturation" are much larger than previously believed. They allege that the Institute of Medicine (IoM) and the NIH have failed to respond to an open letter from a number of scientists and medical researchers, notably Doctors Steve Hickey, Hilary Roberts, Ian Brighthope, Robert Cathcart, Abram Hoffer, Archie Kalokerinos, Tom Levy, Richard Passwater, Hugh Riordan, Andrew Saul and Patrick Holford, which called for revision of the RDI (Reference Daily Intake).

[edit] See also

[edit] Further reading

Books

[edit] 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. Cited in HYPOASCORBEMIA-240400. Online Mendeleian 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. "Although there is still controversy regarding anticancer effects of vitamin C, the use of vitamin C is considered a safe and effective therapy to improve the quality of life of terminal cancer patients".
  4. ^ a b 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
    The study underwent rigorous case reporting standards as outlined by the U.S. National Cancer Institute.
  5. ^ Vitamin C (Ascorbic Acid). University of Maryland Medical Center (April 2002). Retrieved on 2007-02-19.
  6. ^ a b c 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. 
  7. ^ [1] Supplement Watch
  8. ^ H. Hemilia (1996). "Does Vitamin C Alleviate the Symptoms of the Common Cold?". Scand J Infect Dis 26 (1). 
  9. ^ H. Hemilia (1996). "Vitamin C Supplementation and Common Cold Symptoms: Problems with Inaccurate Reviews". Nutrition 12 (11): 804. doi:10.1016/S0899-9007(96)00223-7. 
  10. ^ 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.
  11. ^ Rath M, Linus P. Hypothesis: Lipoprotein (a) is a surrogate for ascorbate. Proc Natl Acad Sci USA. Vol 87, 6204–6207, Aug 1990.
  12. ^ Kniffin CL, McKusick VA, Brennan P. APOLIPOPROTEIN(a); LPA. OMIMTM - Online Mendelian Inheritance in Man, Johns Hopkins University. 1986–2006
  13. ^ Jim English and Hyla Cass. Vitamin C & Heart Health - Linus Pauling’s Collagen Connection. Vitamin Research Products. Retrieved on 2007-02-19.
  14. ^ Jane Higdon (01/31/2006). Vitamin C. Linus Pauling Institute. Retrieved on 2007-02-19.
  15. ^ Frederick Robert Klenner. Significance of High Daily Intake of Ascorbic Acid in Preventive Medicine. AscorbateWeb. Retrieved on 2007-02-19.
  16. ^ 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.
  17. ^ a b ROBERT F. CATHCART III (1996). Preparation of Sodium Ascorbate for IV and IM Use. orthomed.com. Retrieved on 2007-02-21.
  18. ^ SUREFIRE CURES FOR THE COMMON COLD OR THE FLU!. The Vitamin C Foundation. Retrieved on 2007-02-19.
  19. ^ [2]Common Questions About Diet and Cancer
  20. ^ 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
  21. ^ 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
  22. ^ [3] Reciprocal effects of ascorbate on cancer cell growth and the expression of matrix metalloproteinases and transforming growth factor-beta
  23. ^ Qi Chen et al. "Pharmacologic ascorbic acid concentrations selectively kill cancer cells." Proceedings of the National Academy of Sciences of the United States of America (PNAS) 102(38) 13604–13609. PMID 16157892
  24. ^ FDA OKs vitamin C trial for cancer. Physorg.com (January 12, 2007). Retrieved on 2007-04-06. “Federal approval of a clinical trial on intravenous vitamin C as a cancer treatment lends credence to alternative cancer care, U.S. researchers said.”
  25. ^ Study of High-Dose Intravenous (IV) Vitamin C Treatment in Patients With Solid Tumors. Retrieved on 2007-08-02. “The primary purpose of this study is to evaluate the safety and tolerability of vitamin C (ascorbic acid) given by injection into the vein. The second and third purpose of conducting this study is to observe any evidence of tumor response to the vitamin C and compare the level of fatigue (weakness), pain control, ability to do things, and quality of life, before and after vitamin C is given. (Phase I)”
  26. ^ [4]September 2007 - study funded by the NIH at John Hopkins University on the cancer stopping mechanism of Vitamin C
  27. ^ '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.
  28. ^ Vitamin Supplement Use and Mortality. Retrieved on 2008-01-10.
  29. ^ Bowel Titration>.
  30. ^ Dr Dan Rutherfor>.
  31. ^ [Nankivell BJ, Murali KM. Renal failure from vitamin C after transplantation. New England J Med 358(4)e4, Jan 28, 2008], access online
  32. ^ Safety (MSDS) data for ascorbic acid. Oxford University (October 9, 2005). Retrieved on 2007-02-21.
  33. ^ 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).”
  34. ^ [5] Vitamin C produces gene-damaging compounds Accessed July 2007
  35. ^ Balz Frei, Ph.D. (November , 2001). Vitamin C Doesn't Cause Cancer!. Oregon State University. Retrieved on 2007-02-21.
  36. ^ [6] Caspase-8 dependent TRAIL-induced apoptosis in cancer cell lines is inhibited by Vitamin C and catalase.
  37. ^ 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. 
  38. ^ Balz Frei, Ph.D. (November , 2001). Vitamin C Doesn't Cause Cancer!. Oregon State University. Retrieved on 2007-02-21.
  39. ^ [7] Too much of a good thing? Large doses of vitamin C linked to atherosclerosis
  40. ^ 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. 
  41. ^ Massey LK, Liebman M, Kynast-Gales SA (July 2005). "Ascorbate increases human oxaluria and kidney stone risk". J Nutr 123 (7): 1673. PMID 15987848. 
  42. ^ Stephen Lawson (November , 1999). What About Vitamin C and Kidney Stones?. The Linus Pauling Institute. Retrieved on 2007-02-21.
  43. ^ acu-cell
  44. ^ 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. 
  45. ^ 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. 
  46. ^ Vitamin C A Home Abortion Remedy?
  47. ^ 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)
  48. ^ [8]Klenner's "primary and lasting benefits in pregnancy"
  49. ^ Harri Hemilä (January 2006). Do vitamins C and E affect respiratory infections?. University of Helsinki. Retrieved on 2007-02-21.
  50. ^ Bourne G. H. (1949). Vitamin C and immunity. Brit. J. Nutrit., 2: 341-346.
  51. ^ Stone I (1966). "On the genetic etiology of scurvy". Acta geneticae medicae et gemellologiae 15 (4): 345–50. PMID 5971711. 
  52. ^ 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. 
  53. ^ 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)”
  54. ^ 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. 
  55. ^ 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. 
  56. ^ 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.
  57. ^ 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. 
  58. ^ 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. 
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