![]() |
![]() |
|
|
|
IN THIS ARTICLE ![]()
PTSD (post traumatic stress disorder) causes memory problems which make learning more difficult. more... ![]() ![]() OTHER TOPICS Can vitamin C and an apple a day keep cancer away? The value of nutritional supplements ![]() |
Vitamin C, Nutrition and Disease Yi Li, B.Sc., and Herb E. Schellhorn, Ph.D. Y. Li is a graduate student and Dr. Schellhorn is a Professor, Department of Biology, McMaster University, Hamilton, Ontario, Canada. Most of us know about the perils of too little vitamin C from our studies of history: the stories of the explorers, sailors and colonists who, deprived of fresh fruits and vegetables on long sea voyages, developed scurvy, which often caused serious illness and death. During the period of European colonial expansion, finding a cure for scurvy was not only a major medical problem but also a military and economic imperative for any nation with global ambitions. It also proved to be difficult, despite the enormous attention devoted to it, because of medicine's poor understanding of the disease. Today we know that the answer turned out to be Vitamin C, a simple substance that not only cures and prevents scurvy but also has other potential therapeutic effects, which are still being discovered today. Vitamin C is a generic term used to describe all ascorbate compounds, including ascorbic acid, dehydroascorbic acid and ascorbate salts. (The term "vitamin" comes from "vital amine," a term coined in the early 20th century. This is somewhat of a misnomer because these we know now that these compounds do not have any amino groups. However, the term "vitamin" has gained such popularity that it has stuck.) Because of its effect against an array of diseases, vitamin C has been credited with almost magical properties. Although using it to treat diseases such as cancer and heart disease remains controversial, the importance of vitamin C in human health is universally recognized. As one authority rightly put it, "Nothing emphasizes the importance of vitamin C to human beings more than the effect of being without it for a relatively short time."1 Animals Do It; We Can't L-ascorbic acid, a naturally-occurring and biologically active form of vitamin C, exists as white crystals and is freely soluble in water. Most non-human animals can make their own vitamin C, but humans cannot. We must rely instead on eating foods that contain vitamin C in order to survive. This state of affairs -- in effect a nutritional defect of our species -- was caused by a genetic mutation estimated to have occurred around 40 million years ago.2 The fact that this mutation spread throughout the human population raises the question of whether or not this "nutritional defect" is associated with certain evolutionary advantages. While the answer to this question is unknown, several hypotheses have been proposed.3,4,5 For example, some scientists speculate that the ultimate cause was a prehistoric viral infection that caused genetic damage which knocked out our ability to manufacture vitamin C. But because our ancestors lived in warm climates that were extremely rich in foods containing vitamin C, the nutritional consequences of this defect didn't really show up. As this theory has it, this inability to produce vitamin C internally likely caused an accumulation of free radicals within the body (as discussed below), which, in turn, resulted in an increase in the mutation rate of bodily cells, which, in turn, sped up the evolutionary transition to modern day Homo sapiens. This idea of ascorbic acid influencing the rate of mutation and, consequently, evolution is supported by the fact that increased levels of free radicals are known to promote HIV replication, whereas ascorbic acid slows down the replication cycle.6 This could be one reason why natural selection favored the loss of our ability to synthesize vitamin C, especially when vitamin C is available from diet. By reducing human longevity, the loss of vitamin C producing-ability may also have selected against aging populations and made more food available for younger and more fertile individuals within early human populations, perhaps in a time of food shortages -- in effect, thinning the human herd to the ultimate benefit of the survival of the species. What Vitamin C Does for Your Body The healing power of foods containing vitamin C had been understood long before the discovery of the vitamin itself. As early as 17th century, more than three hundred years before the chemistry of ascorbic acid was known, lemon juice was used by some to help prevent scurvy and treat the tooth loss, broken blood vessels and impaired wound healing associated with it. These symptoms are the result of a collagen deficiency brought on by a lack of vitamin C.7 Vitamin C affects mood and energy levels. Depression and hypochondria are common symptoms of vitamin C deficiency.8 These are caused by norepinephrine deficiency, which results from the inadequate conversion of dopamine to norepinephrine in the absence of ascorbic acid.9 Vitamin C deprivation often also leads to a condition that impairs fatty acid metabolism and produces fatigue and lethargy.10 Vitamin C is also essential for the absorption of iron by our bodies. Lack of vitamin C can lead to iron deficiency anemia, which is characterized by pallor, fatigue and weakness.11,12,13,14 How We Process Vitamin C When we take vitamin C, it is absorbed in the small intestine and enters the circulatory system from there.15,16,17 While circulating in the blood, vitamin C is filtered by the kidneys. The filtered vitamin C is then reabsorbed into the blood.18 There are limits, however, to the amount of vitamin C that the body can process.19,20,21 Excess vitamin C, as a water-soluble vitamin, is simply excreted into the urine. For this reason, taking large quantities of vitamin C orally cannot raise and maintain ascorbic acid levels in the blood. The bottom line is that vitamin C cannot be stored for long periods in our bodies. We need to take in a consistent supply of vitamin C through our diet. How Much Vitamin C Should We Take? The current recommended daily allowance (RDA) for vitamin C, set by the Food and Nutrition Board of the U.S. National Academy of Sciences, is 75 mg per day for adult women and 90 mg per day for adult men. This value is derived from the estimated average requirement or vitamin C, which is the amount of vitamin C required by half of the healthy population at a certain life stage. Another RDA, however, based on the adequate intake (AI) value, has also been proposed. The AI value is calculated from a group of healthy individuals and so is more useful for establishing the best levels of nutrient intake for individuals.12 Based on this value, it is recommended that 200 mg of vitamin C should be taken per day. This equals about 5 servings of fruits and vegetables. At this level, our bodily tissues will soon absorb the maximum amount of vitamin C that is possible. Although vitamin C can come from a variety of sources, including dietary supplements, the best way to get vitamin C is directly from the food we eat. Therefore, 5 servings of fruits and vegetables are recommended for all healthy individuals under normal conditions ).12 Vitamin C and Cigarettes People who smoke and those who are exposed to cigarette smoking need more vitamin C than those who don't smoke or are not exposed. Cigarette smoke contains free radicals which deplete vitamin C.22 Smoking can reduce serum vitamin C levels by up to 40%.23 Nevertheless, taking moderate doses of vitamin C supplements can efficiently restore proper vitamin C levels in smokers.24 Vitamin C and Iron Vitamin C facilitates our body's absorption of iron.25 While this is definitely a good thing, a small percentage of the population suffers from a condition called hereditary hemochromatosis, which can cause them too absorb too much iron, which in turn can damage cells and tissue. In most cases, these people should avoid taking vitamin C supplements.26 The frequency of hereditary hemochromatosis in Caucasian populations is 0.4-1%,27 and it can be identified with a simple test. Your doctor should run one of these tests before recommending that you or a loved one take extra vitamin C. Kidney Stones One of the byproducts left over after the body metabolizes ascorbic acid is a substance called oxalate,28 which can help cause a type of kidney stones.29,30 While studies on the question of whether or not taking vitamin C leads directly to kidney stone formation have been inconclusive, people who are prone to kidney stones should talk to their doctor before taking vitamin C.31,32 The Best Sources of Vitamin C Fresh fruits and vegetables are the best sources of vitamin C. Some of the more common dietary sources of vitamin C are listed in Table 1. It should be noted, however, that vitamin C content can depend on how food is stored and prepared. For example, boiling vegetables may result in 50% to 80% vitamin C loss. Lack of freshness can also significantly reduce vitamin C content. Table 1. Dietary Sources of Vitamin C.
Levine et al. 1999. Criteria and Recommendations for vitamin C intake JAMA. 281:1415-1423. (used with permission). Vitamin C as Health Therapy? Vitamin C's Effects on Cancer The potential anti-cancer effect of vitamin C is a controversial topic. Using vitamin C for cancer prevention and treatment was first proposed in 1949, and was supported by a number of physicians and scientists, (including Linus Pauling), who showed that the survival rate of terminal cancer patients could be improved by giving them high-dose, intravenous vitamin C.33,34,35 However, a later study at the Mayo Clinic, using randomized, placebo-controlled methodology, cast doubt on the effectiveness and reliability of megadose vitamin C therapy. Some of the difference in these findings may be attributable, at least in part, to the difference in how the vitamin C was given. In the 1974 study, vitamin C was delivered by mouth and intravenously, whereas in the Mayo Clinic study it was administered by mouth only. As we have said, there is a limit to how much vitamin C can reach the bloodstream when it is taken orally. Much higher levels can be achieved, however, if the vitamin C is administered intravenously. Therefore, it is likely that higher effective vitamin C concentration was achieved in the earlier study than in the Mayo Clinic study. Despite extensive research and public attention over the years, vitamin C has not yet been proven effective in treating cancer.36,37,38 Recent research has, however, identified mechanisms that may explain whatever anti-cancer properties vitamin C may have. As a potent antioxidant, vitamin C protects cells from oxidative DNA damage, a known cause of cancer.39,40,41,42,43,44 In addition to its direct antioxidant effects, vitamin C makes cancerous cells more susceptible to apoptosis, or programmed cell death.45,46,47,48 Vitamin C also helps prevent uncontrolled cell proliferation, which contributes to cancer growth.49,50,51,52,53,54 This research shows how vitamin C could function as an anti-cancer agent. In light of these new developments, an interventional study using high-dose intravenous vitamin C in the treatment of cancer in human subjects was approved by the FDA and entered phase I trial in 2007. This is the first officially-conducted interventional study examining the anti-cancer] effect of vitamin C and its findings, which are expected in 2009, should yield information that will help determine the value of this vitamin as a cancer fighter. Vitamin C's Effects on Cardiovascular Disease Since oxidative damage also contributes to cardiovascular disease, ascorbic acid may have a positive effect on heart disease. Epidemiological studies have confirmed that eating vitamin C-rich foods such as fresh fruits and vegetables is associated with a reduced risk of cardiovascular disease.55,56,57 However, because people who eat healthy diets tend to live generally healthy lifestyles (not smoking or drinking to excess, for example), it is unclear whether vitamin C is really the causal factor in the reduction of heart disease. Some studies have actually found the opposite.58 As with cancer, in recent years scientists have changed their focus from trying to find a "cure" to identifying possible mechanisms by which ascorbic acid might interfere with heart disease-inducing processes. Cardiovascular disease often begins with oxidative damage from naturally- occurring substances such as reactive oxygen (ROS) or reactive nitrogen species (RNS). Accumulation of these substances in the body has several detrimental effects on the cardiovascular system. First, they modify low density lipoprotein (LDL), leading to the formation of highly reactive oxidized LDL (oxLDL) cells,59,60,61 which are more likely to clog blood vessels,62,63 promote inflammation,64,65 and cause the death of cells lining the blood vessels.66,67 These events are the precursors of artery-clogging atherosclerotic lesions. Vitamin C interferes with these processes in a number of ways. For example, ascorbic acid reduces the amount of ROS and RNS in the blood.68 It makes LDL more resistant to oxidation and thus slows the formation of oxLDL. Vitamin C also counteracts oxLDL-induced inflammation69,70,71,72 and cell death,73,74 preventing the formation of lesions within the blood vessels.75,76,77,78,79,80,81 The anti-atherosclerotic properties of ascorbic acid are significantly increased when it is combined with vitamin E.82 The cooperative interactions between these two vitamins form the basis for co-antioxidant therapy in the treatment of heart disease, which is becoming increasingly accepted by the medical community.83,84,85,86,87,88,89 Conclusions While vitamin C is essential for the healthy functioning of the human body, its role in treating diseases such as cancer and heart disease has not yet been proven. Nevertheless, intensive research has shed light on the molecular mechanisms by which vitamin C interferes with disease-related processes. For example, the ability of vitamin C to selectively target and kill cancer cells, among other things, suggests that vitamin C may be a potential anti-cancer agent. In addition, completely unexpected functions of vitamin C that may have important medical implications have recently been discovered. For example, ascorbic acid stimulated transformation of mouse embryonic stem cells into cardiac muscle cells, which may ultimately result in cardiac tissue regeneration for heart transplantation. While in the early stages, the applications of this new knowledge regarding vitamin C hold great promise. Recommended Articles Vitamin C in Advanced Therapy of Cancer and Cardiovascular Disease
References 1. Davies,M., Austin,J. & Partridge,D.A. Vitamin C: Its Chemistry and Biochemistry., pp. 74-96 (Royal Society of Chemistry, Letchworth,1991). return 2. Nishikimi,M., Koshizaka,T., Ozawa,T. & Yagi,K. Occurrence in humans and guinea pigs of the gene related to their missing enzyme L-gulono-gamma-lactone oxidase. Arch. Biochem. Biophys. 267, 842-846 (1988). return 3. Challem,J.J. Did the loss of endogenous ascorbate propel the evolution of Anthropoidea and Homo sapiens? Med. Hypotheses 48, 387-392 (1997). return 4. Chatterjee,I.B. Evolution and the biosynthesis of ascorbic acid. Science 182, 1271-1272 (1973). return 5. Millar,J. Vitamin C--the primate fertility factor? Med. Hypotheses 38, 292-295 (1992). return 6. Benzie,I.F. Evolution of dietary antioxidants. Comp Biochem. Physiol A Mol. Integr. Physiol 136, 113-126 (2003). return 7. Murad,S. et al. Regulation of collagen synthesis by ascorbic acid. Proc. Natl. Acad. Sci. U. S. A 78, 2879-2882 (1981). return 8. Diliberto,E.J., Daniels,A.J. & Viveros,O.H. Multicompartmental Secretion of Ascorbate and Its Dual Role in Dopamine Beta-Hydroxylation. Am J Clin Nutr 54, S1163-S1172 (1991). return 9. Rebouche,C.J. Ascorbic-Acid and Carnitine Biosynthesis. Am J Clin Nutr 54, S1147-S1152 (1991). return 10. Ha,T.Y., Otsuka,M. & Arakawa,N. The Regulatory Effect of Ascorbate on the Carnitine Synthesis in Primary Cultured Guinea-Pig Hepatocytes. Journal of Nutritional Science and Vitaminology 37, 371-378 (1991). return 11. Hallberg,L., Brune,M. & Rossander,L. Effect of Ascorbic-Acid on Iron-Absorption from Different Types of Meals - Studies with Ascorbic-Acid-Rich Foods and Synthetic Ascorbic-Acid Given in Different Amounts with Different Meals. Human Nutrition-Applied Nutrition 40A, 97-113 (1986). return 12. Levine,M., Rumsey,S.C., Daruwala,R., Park,J.B. & Wang,Y.H. Criteria and recommendations for vitamin C intake. JAMA 281, 1415-1423 (1999). return 13. Herbert,V., Shaw,S. & Jayatilleke,E. Vitamin C-driven free radical generation from iron. Journal of Nutrition 126, S1213-S1220 (1996). return 14. Siegenberg,D. et al. Ascorbic-Acid Prevents the Dose-Dependent Inhibitory Effects of Polyphenols and Phytates on Nonheme-Iron Absorption. Am J Clin Nutr 53, 537-541 (1991). return 15. Hornig,B., Arakawa,N., Kohler,C. & Drexler,H. Vitamin C improves endothelial function of conduit arteries in patients with chronic heart failure. Circulation 97, 363-368 (1998). return 16. Malo,C. & Wilson,J.X. Glucose modulates vitamin C transport in adult human small intestinal brush border membrane vesicles. Journal of Nutrition 130, 63-69 (2000). return 17. Takanaga,H., Mackenzie,B. & Hediger,M.A. Sodium-dependent ascorbic acid transporter family SLC23. Pflugers Arch 447, 677-682 (2004). return 18. Ralli,E.P., Friedman,G.J. & Rubin,S.H. The Mechanism of the Excretion of Vitmain C by the Human Kidney. J. Clin. Invest 17, 765-770 (1938). return 19. Wilson,J.X. Regulation of Vitamin C Transport. Annual Review of Nutrition 25, 105-125 (2005). return 20. Padayatty,S.J. et al. Vitamin C pharmacokinetics: Implications for oral and intravenous use. Annals of Internal Medicine 140, 533-537 (2004). return 21. Levine,M. et al. Vitamin C pharmacokinetics in healthy volunteers: Evidence for a recommended dietary allowance. Proc Natl Acad Sci USA 93, 3704-3709 (1996). return 22. Lykkesfeldt,J. et al. Ascorbate is depleted by smoking and repleted by moderate supplementation: a study in male smokers and nonsmokers with matched dietary antioxidant intakes. Am J Clin Nutr 71, 530-536 (2000). return 23. Ross,M.A. et al. Plasma-Concentrations of Carotenoids and Antioxidant Vitamins in Scottish Males - Influences of Smoking. Eur J Clin Nutr 49, 861-865 (1995). return 24. Northrop-Clewes,C.A. & Thurnham,D.I. Monitoring micronutrients in cigarette smokers. Clinica Chimica Acta 377, 14-38 (2007).. return 25. Nienhuis,A.W. Vitamin-C and Iron. New England Journal of Medicine 304, 170-171 (1981). return 26. Fraga,C.G. & Oteiza,P.I. Iron toxicity and antioxidant nutrients. Toxicology 180, 23-32 (2002). return 27. Adams,P.C. Population screening for hemochromatosis. Hepatology 29, 1324-1327 (1999). return 28. Hellman,N.L. & Burns,J.J. Metabolism of L-ascorbic acid-1-C14 in man. J. Biol. Chem. 230, 923-930 (1958). return 29. Chalmers,A.H., Cowley,D.M. & Brown,J.M. A possible etiological role for ascorbate in calculi formation. Clin. Chem. 32, 333-336 (1986). return 30. Baxmann,A.C., De,O.G.M. & Heilberg,I.P. Effect of vitamin C supplements on urinary oxalate and pH in calcium stone-forming patients. Kidney Int. 63, 1066-1071 (2003). return 31. Curhan,G.C., Willett,W.C., Rimm,E.B. & Stampfer,M.J. A prospective study of the intake of vitamins C and B6, and the risk of kidney stones in men. J. Urol. 155, 1847-1851 (1996). return 32. Curhan,G.C., Willett,W.C., Speizer,F.E. & Stampfer,M.J. Intake of vitamins B6 and C and the risk of kidney stones in women. J. Am. Soc. Nephrol. 10, 840-845 (1999). return 33. Cameron,E. & Campbell,A. The orthomolecular treatment of cancer. II. Clinical trial of high-dose ascorbic acid supplements in advanced human cancer. Chem Biol Interact 9, 285-315 (1974). return 34. Cameron,E. & Pauling,L. Supplemental ascorbate in the supportive treatment of cancer: Prolongation of survival times in terminal human cancer. Proc Natl Acad Sci USA 73, 3685-3689 (1976). return 35. Cameron,E. & Pauling,L. Supplemental ascorbate in the supportive treatment of cancer: reevaluation of prolongation of survival times in terminal human cancer. Proc Natl Acad Sci USA 75, 4538-4542 (1978). return 36. Moertel,C.G. 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 312, 137-141 (1985). return 37. Li,Y. & Schellhorn,H.E. Can ageing-related degenerative diseases be ameliorated through administration of vitamin C at pharmacological levels? Med Hypotheses (2006). return 38. Li,Y. & Schellhorn,H.E. New developments and novel therapeutic perspectives for vitamin C. J. Nutr. 137, 2171-2184 (2007). return 39. Buettner,G.R. The Pecking Order of Free-Radicals and Antioxidants - Lipid-Peroxidation, Alpha-Tocopherol, and Ascorbate. Archives of Biochemistry and Biophysics 300, 535-543 (1993). return 40. Deng,X.S., Tuo,J.S., Poulsen,H.E. & Loft,S. Prevention of oxidative DNA damage in rats by Brussels sprouts. Free Radical Research 28, 323-333 (1998). return 41. Fraga,C.G. et al. Ascorbic-Acid Protects Against Endogenous Oxidative Dna Damage in Human Sperm. Proc Natl Acad Sci USA 88, 11003-11006 (1991). return 42. Rehman,A., Bourne,L.C., Halliwell,B. & Rice-Evans,C.A. Tomato consumption modulates oxidative DNA damage in humans. Biochemical and Biophysical Research Communications 262, 828-831 (1999). return 43. Thompson,H.J. et al. Effect of increased vegetable and fruit consumption on markers of oxidative cellular damage. Carcinogenesis 20, 2261-2266 (1999). return 44. Chen,Q. et al. Pharmacologic ascorbic acid concentrations selectively kill cancer cells: Action as a pro-drug to deliver hydrogen peroxide to tissues. Proc Natl Acad Sci USA 102, 13604-13609 (2005). return 45. Catani,M.V. et al. Ascorbate up-regulates MLH1 (Mut L homologue-1) and p73: implications for the cellular response to DNA damage. Biochemical Journal 364, 441-447 (2002). return 46. Bowie,A.G. & O'Neill,L.A. Vitamin C inhibits NF-kappa B activation by TNF via the activation of p38 mitogen-activated protein kinase. J Immunol 165, 7180-7188 (2000). return 47. Carcamo,J.M., Pedraza,A., Borquez-Ojeda,O. & Golde,D.W. Vitamin C suppresses TNF alpha-induced NF kappa B activation by inhibiting I kappa B alpha phosphorylation. Biochemistry 41, 12995-13002 (2002). return 48. Han,S.S. et al. L-ascorbic acid represses constitutive activation of NF-kappaB and COX-2 expression in human acute myeloid leukemia, HL-60. J Cell Biochem 93, 257-270 (2004). return 49. Thomas,C.G., Vezyraki,P.E., Kalfakakou,V.P. & Evangelou,A.M. Vitamin C transiently arrests cancer cell cycle progression in S phase and G2/M boundary by modulating the kinetics of activation and the subcellular localization of Cdc25C phosphatase. Journal of Cellular Physiology 205, 310-318 (2005). return 50. Gao,P. et al. HIF-dependent antitumorigenic effect of antioxidants in vivo. Cancer Cell 12, 230-238 (2007). return 51. Knowles,H.J., Raval,R.R., Harris,A.L. & Ratcliffe,P.J. Effect of ascorbate on the activity of hypoxia-inducible factor in cancer cells. Cancer Res. 63, 1764-1768 (2003). return 52. Leo,C., Giaccia,A.J. & Denko,N.C. The hypoxic tumor microenvironment and gene expression. Semin. Radiat. Oncol. 14, 207-214 (2004). return 53. Vaupel,P. The role of hypoxia-induced factors in tumor progression. Oncologist. 9 Suppl 5, 10-17 (2004). return 54. Harris,A.L. Hypoxia - A key regulatory factor in tumour growth. Nature Reviews Cancer 2, 38-47 (2002). return 55. Block,G., Norkus,E., Hudes,M., Mandel,S. & Helzlsouer,K. Which plasma antioxidants are most related to fruit and vegetable consumption? Am J Epidermiol 154, 1113-1118 (2001). return 56. Joshipura,K.J. et al. The effect of fruit and vegetable intake on risk for coronary heart disease. Ann Intern Med 134, 1106-1114 (2001). return 57. Liu,S. et al. Fruit and vegetable intake and risk of cardiovascular disease: the Women's Health Study. Am J Clin Nutr 72, 922-928 (2000). return 58. Muntwyler,J., Hennekens,C.H., Manson,J.E., Buring,J.E. & Gaziano,J.M. Vitamin supplement use in a low-risk population of US male physicians and subsequent cardiovascular mortality. Arch Intern Med 162, 1472-1476 (2002). return 59. Stocker,R. & Keaney,J.F. Role of oxidative modifications in atherosclerosis. Physiol Rev 84, 1381-1478 (2004). return 60. de Villiers,W.J.S. & Smart,E.J. Macrophage scavenger receptors and foam cell formation. J Leukoc Biol 66, 740-746 (1999). return 61. Li,A.C. & Glass,C.K. The macrophage foam cell as a target for therapeutic intervention. Nat Med 8, 1235-1242 (2002). return 62. Parthasarathy,S., Quinn,M.T., Schwenke,D.C., Carew,T.E. & Steinberg,D. Oxidative Modification of Beta-Very Low-Density Lipoprotein - Potential Role in Monocyte Recruitment and Foam Cell-Formation. Arteriosclerosis 9, 398-404 (1989). return 63. Quinn,M.T., Parthasarathy,S., Fong,L.G. & Steinberg,D. Oxidatively modified low density lipoproteins: a potential role in recruitment and retention of monocyte/macrophages during atherogenesis. Proc Natl Acad Sci USA 84, 2995-2998 (1987). return 64. Ross,R. Atherosclerosis is an inflammatory disease. Am Heart J 138, S419-S420 (1999). return 65. Stoll,G. & Bendszus,M. Inflammation and atherosclerosis - Novel insights into plaque formation and destabilization. Stroke 37, 1923-1932 (2006). return 66. Dimmeler,S., Haendeler,J., Galle,J. & Zeiher,A.M. Oxidized low-density lipoprotein induces apoptosis of human endothelial cells by activation of CPP32-like proteases - A mechanistic clue to the 'response to injury' hypothesis. Circulation 95, 1760-1763 (1997). return 67. Harada-Shiba,M., Kinoshita,M., Kamido,H. & Shimokado,K. Oxidized low density lipoprotein induces apoptosis in cultured human umbilical vein endothelial cells by common and unique mechanisms. J Biol Chem 273, 9681-9687 (1998). return 68. Retsky,K.L., Freeman,M.W. & Frei,B. Ascorbic acid oxidation product(s) protect human low density lipoprotein against atherogenic modification. Anti- rather than prooxidant activity of vitamin C in the presence of transition metal ions. J Biol Chem 268, 1304-1309 (1993). return 69. Griffiths,H., Rayment,S., Shaw,J., Lunec,J. & Woollard,K. Dietary supplementation with vitamin C but not vitamin E reduces constitutive expression of ICAM-1 in peripheral blood monocytes of normal subjects with low plasma vitamin C levels. Free Radic Biol Med 35, S35 (2003). return 70. Mo,S.J., Son,E.W., Rhee,D.K. & Pyo,S. Modulation of TNF-alpha-induced ICAM-1 expression, NO and H2O2 production by alginate, allicin and ascorbic acid in human endothelial cells. Arch Pharm Res 26, 244-251 (2003). return 71. Rayment,S.J., Shaw,J., Woollard,K.J., Lunec,J. & Griffiths,H.R. Vitamin C supplementation in normal subjects reduces constitutive ICAM-1 expression. Biochem Biophys Res Commun 308, 339-345 (2003). return 72. Son,E.W., Mo,S.J., Rhee,D.K. & Pyo,S. Vitamin C blocks TNF-alpha-induced NF-kappaB activation and ICAM-1 expression in human neuroblastoma cells. Arch Pharm Res 27, 1073-1079 (2004). return 73. Asmis,R. & Wintergerst,E.S. Dehydroascorbic acid prevents apoptosis induced by oxidized low-density lipoprotein in human monocyte-derived macrophages. Eur J Biochem 255, 147-155 (1998). return 74. Siow,R.C.M., Richards,J.P., Pedley,K.C., Leake,D.S. & Mann,G.E. Vitamin C protects human vascular smooth muscle cells against apoptosis induced by moderately oxidized LDL containing high levels of lipid hydroperoxides. Arterioscler Thrombosis Vasc Biol 19, 2387-2394 (1999). return 75. Baker,R.A., Milstien,S. & Katusic,Z.S. Effect of vitamin C on the availability of tetrahydrobiopterin in human endothelial cells. J Cardiovasc Pharm 37, 333-338 (2001). return 76. Heller,R. et al. L-ascorbic acid potentiates endothelial nitric oxide synthesis via a chemical stabilization of tetrahydrobiopterin. J Biol Chem 276, 40-47 (2001). return 77. Huang,A., Vita,J.A., Venema,R.C. & Keaney,J.F. Ascorbic acid enhances endothelial nitric-oxide synthase activity by increasing intracellular tetrahydrobiopterin. J Biol Chem 275, 17399-17406 (2000). return 78. Marui,N. et al. Vascular Cell-Adhesion Molecule-1 (Vcam-1) Gene-Transcription and Expression Are Regulated Through An Antioxidant Sensitive Mechanism in Human Vascular Endothelial-Cells. J Clin Invest 92, 1866-1874 (1993). return 79. Ignarro,L.J., Buga,G.M., Wood,K.S., Byrns,R.E. & Chaudhuri,G. Endothelium-Derived Relaxing Factor Produced and Released from Artery and Vein Is Nitric-Oxide. Proc Natl Acad Sci USA 84, 9265-9269 (1987). return 80. de Sousa,M.G. et al. Ascorbic acid improves impaired venous and arterial endothelium-dependent dilation in smokers. Acta Pharmacol Sin 26, 447-452 (2005). return 81. Plantinga,Y. et al. Supplementation with vitamins C and E improves arterial stiffness and endothelial function in essential hypertensive patients. Am J Hyper 20, 392-397 (2007). return 82. Carr,A.C., Zhu,B.Z. & Frei,B. Potential antiatherogenic mechanisms of ascorbate (vitamin C) and alpha-tocopherol (vitamin E). Circ Res 87, 349-354 (2000). return 83. Antoniades,C. et al. Effects of antioxidant vitamins C and E on endothelial function and thrombosis/fibrinolysis system in smokers. Thromb Haemost 89, 990-995 (2003). return 84. Engler,M.M. et al. Antioxidant vitamins C and E improve endothelial function in children with hyperlipidemia: Endothelial Assessment of Risk from Lipids in Youth (EARLY) Trial. Circulation 108, 1059-1063 (2003). return 85. Fang,J.C. et al. Effect of vitamins C and E on progression of transplant-associated arteriosclerosis: a randomised trial. Lancet 359, 1108-1113 (2002). return 86. Liu,L.P. & Meydani,M. Combined vitamin C and E supplementation retards early progression of arteriosclerosis in heart transplant patients. Nutr Rev 60, 368-371 (2002). return 87. Tousoulis,D. et al. Effects of combined administration of vitamins C and E on reactive hyperemia and inflammatory process in chronic smokers. Atherosclerosis 170, 261-267 (2003). return 88. Guo,X.M. et al. Creation of engineered cardiac tissue in vitro from mouse embryonic stem cells. Circulation 113, 2229-2237 (2006). return 89. Takahashi,T. et al. Ascorbic acid enhances differentiation of embryonic stem cells into cardiac myocytes. Circulation 107, 1912-1916 (2003). return |
|||||||||||||||||||||||||||||||||||||||||||||||||
|
|
|
|
||||||||||||||||||||||||||||||||||||||||||||||||
|
NEWS SEARCH CONTENTS MEDITORIAL ASK DISCUSS REGISTER HELP HOME |
||||||||||||||||||||||||||||||||||||||||||||||||||
© 2008 interMDnet Corporation. All Rights Reserved. PRIVACY POLICY |
||||||||||||||||||||||||||||||||||||||||||||||||||