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Garlic modulates lipid peroxidation and antioxidant status during N-Nitrosodiethylamine-induced hepatic tumorigenesis

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Abstract

Effects of garlic (Allium sativum Linn.) on circulatory lipid peroxidation and antioxidant status were evaluated in N-Nitrosodiethylamine-induced hepatocarcinogenesis in male rats. Enhanced lipid peroxidation in the circulation of N-Nitrosodiethylamine (NDEA) treated rats was accompanied by a significant decrease in the levels of Β carotene, ascorbic acid, vitamin E, reduced glutathione (GSH), glutathione peroxidase (GPx), superoxide dismutase (SOD) and catalase (CAT). Garlic administered rats experienced a significant reduction in lipid peroxidation with a simultaneous elevation in antioxidant levels. Researchers hypothesize that the presence of organosulphur compounds could have decreased lipid peroxidation and increased antioxidant levels in NDEA administered rats.

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References

  1. Schaff ZS, Lapis K, Henson DE (1993) Liver. In: Hensan DE, Albores Saavedra J (eds), Pathology of Incipient Neoplasma. Philadelphia: Saunders, pp 151–166.

    Google Scholar 

  2. Tricker AR, Pfundstein B, Theobald E, Preussman R, Spiegenhalder B (1991) Mean daily intake of volatile N-nitrosamines from foods and beverages in West Germany in 1989–90. Food Chem Toxicol 29: 729–732.

    Google Scholar 

  3. Scanlan RA (1983) Formation and occurrence of nitrosamines in food. Cancer Res (Suppl) 43: 2435S–2440S.

    Google Scholar 

  4. Cerutti PA (1985) Prooxidant states and tumor promotion. Science 227: 375–381.

    Google Scholar 

  5. Ames BN (1989) Endogeneous oxidative DNA damage, aging and cancer. Free Radic Res Comm 7: 121–128.

    Google Scholar 

  6. Dausch JG, Nixon DW (1990) Garlic: A review of its relationship to malignant disease. Prev Med 19: 346–361.

    Google Scholar 

  7. Agarwal KC (1996) Therapeutic actions of garlic constituents. Med Res Rev 16: 111–124.

    Google Scholar 

  8. Yeh YY, Yeh SM (1994) Garlic reduces plasma lipids by inhibiting hepatic cholesterol and tricylglycerol synthesis. Lipids 29: 189–193.

    Google Scholar 

  9. Gao CM, Takezaki T, Ding JH, Li MS, Tajima K (1999) Protective effect of allium vegetables against both esophageal and stomach cancer: A simultaneous case reference study of a high epidemic area in Jiangsu province, China. Jap J Cancer Res 90: 614–621.

    Google Scholar 

  10. Siegers CP, Steffen B, Robke A, Pentz P (1999) The effects of garlic preparations against human tumor cell proliferation. Phytomedicine 6: 7–11.

    Google Scholar 

  11. Hayes JD, Pulford DJ (1995) The glutathione S-transferase supergene family: Regula-tion of GST and the contribution of the isoenzymes to cancer chemoprevention and drug resistance. Crit Rev Biochem Mol Biol 30: 445–600.

    Google Scholar 

  12. Jeena JK, Joy KL, Kuttan R (1999) Effect of Emblica officinalis, Phyllanthus amarus and Picrorhiza kurroa on N-nitrosodiethylamine induced hepatocarcinogenesis. Cancer Lett 29: 43–48.

    Google Scholar 

  13. Singh SP, Abraham SK, Kesavan PC (1996) Radioprotection of mice following garlic pretreatment. Br J Cancer 74: 102–104.

    Google Scholar 

  14. Yagi K (1978) Lipid peroxides and human disease. Chem Physiol Lipids 45: 337–351.

    Google Scholar 

  15. Donnan SK (1950) The thiobarbituric acid test applied to tissues from rats treated in various ways. J Biol Chem 182: 415–419.

    Google Scholar 

  16. Ellman GL (1959) Tissue sulfhydryl groups. Arch Biochem Biophys 82: 70–77.

    Google Scholar 

  17. Bayfield RK, Cole ER (1980) Colorimetric estimation of vitamin A with trichloroacetic acid. Meth Enzymol 67: 189–195.

    Google Scholar 

  18. Baker H, Frank O, De Angelis B, Feingold SE (1980) Plasma tocopherol in man at various times after ingesting free (or) acetylated tocopherol. Nutr Rep Int 21: 521–536.

    Google Scholar 

  19. Omaye ST, Turnbull TD, Sauberlich HE (1979) Selected method for the determination of ascorbic acid in animal cells, tissues and fluids. In: McCormick D, Wright DL (eds), Methods in Enzymology. New York: Academic Press, pp 3–11.

    Google Scholar 

  20. Kakkar P, Das B, Viswanathan PN (1984) A modified spectrophotometric assay of superoxide dismutase. Indian J Biochem Biophys 21: 130–132.

    Google Scholar 

  21. Rotruck JT, Pope AL, Ganther HE, Swanson AB, Hafeman DG, Hoekstra WG (1973) Selenium: Biochemical roles as components of glutathione peroxidase. Science 179: 588–590.

    Google Scholar 

  22. Sinha KA (1972) Colorimetric assay of catalase. Anal Biochem 47: 389–394.

    Google Scholar 

  23. Drabkin DL, Austin JM (1932) Spectrophotometric studies, spectrophotometric con-stants for common haemoglobin derivatives in human, dog and rabbit food. J Biol Chem 98: 719–733.

    Google Scholar 

  24. Anis KV, Rajesh Kumar NV, Kuttan R (2001) Inhibition of chemical carcinogenesis by biberine in rats and mice. J Pharm Pharmacol 53: 763–768.

    Google Scholar 

  25. Dreher D, Junod AF (1996) Role of oxygen free radicals in cancer development. Eur J Cancer 32A: 30–38.

    Google Scholar 

  26. Bartsch H, Hietanen E, Malaveille C (1989) Carcinogenic nitrosamines: Free radical aspects of their action. Free Radic Biol Med 7: 637–644.

    Google Scholar 

  27. Leoppky RN, Li YE (1991) Nitrosamine activation and detoxification through free radicals and their derived cations. In: Neill IKO, Chen J, Bartsch H (eds), Relevance to Human Cancer of Nitroso Compounds, Tobacco and Mycotoxins. Lyon: IARC Scientific Publication No. 105, pp 375–382.

    Google Scholar 

  28. Vina RJ, Sacz ST, Vina C (1989) The pathological functions of glutathione. In: Mignel J, Quintanilla AT, Weber H (eds), Handbook of Free Radicals and Antioxidants in Biomedicine. Boca Raton: CRC Press, pp 121–132.

    Google Scholar 

  29. Niki E (1987) Interaction of ascorbate and á-tocopherol. Ann New York Acad Sci 498: 186–199.

    Google Scholar 

  30. Gerster H (1995) β-Carotene, vitamin E and vitamin C in different stages of experimental carcinogenesis. Eur J Clin Nutr 49: 155–168.

    Google Scholar 

  31. Morrissey PA, Quin PB, Sheehy PJA (1994) Newer aspects of micronutrients in chronic disease: Vitamin E. Proc Natr Soc 53: 571–582.

    Google Scholar 

  32. Fridovich I (1975) Superoxide dismutase. Ann Rev Biochem 44: 147–159.

    Google Scholar 

  33. Mark D, Betram H, Linzuo L, Kuypers FA (1991) Erythrocyte defense against H2O2. Pre-eminent importance of catalase. J Lab Clin Med 118: 7–16.

    Google Scholar 

  34. Eaton JW (1991) Catalase and peroxidase and glutathione and hydrogen peroxide: Mysteries of the bestiary. J Lab Clin Med 118: 3–4.

    Google Scholar 

  35. Corrocher R, Carasil M, Bellisola G et al. (1986) Severe impairment of antioxidant systems in hepatoma. Cancer 58: 1658–1662.

    Google Scholar 

  36. Prasad K, Laxdal VA, Yu M, Raney BL (1996) Evaluation of hydroxyl radical scavenging property of garlic. Mol Cell Biochem 154: 55–63.

    Google Scholar 

  37. Wei Z, Lau BHS (1998) Garlic inhibits free radical generation and augments antioxidant activity in vascular endothelial cells. Nutr Res 18: 61–70.

    Google Scholar 

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Sundaresan, S., Subramanian, P. Garlic modulates lipid peroxidation and antioxidant status during N-Nitrosodiethylamine-induced hepatic tumorigenesis. Plant Foods Hum Nutr 58, 1–8 (2003). https://doi.org/10.1023/B:QUAL.0000040343.85471.24

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