The effects of aqueous extract of white tea on serum antioxidant enzymes in rats exposed to arsenic
Subject Areas :
Veterinary Clinical Pathology
mohammadhassan rasoulifard
1
,
felor zargari
2
1 - گروه زیست شناسی، واحد اهر، دانشگاه آزاد اسلامی، اهر، ایران.
2 - گروه علوم پزشکی، واحد مرند، دانشگاه آزاد اسلامی، مرند، ایران.
Received: 2015-08-15
Accepted : 2015-10-19
Published : 2015-08-23
Keywords:
Antioxidant enzymes,
Oxidative stress,
Arsenic,
White tea,
Abstract :
Oxidative stress is a condition is which the biological system's ability to detoxify and eliminate harmful effects of free radicals is not sufficient and oxidative damages to cells or tissues leads to the development of diseases such as cancer, arteriosclerosis and degenerative changes. Phenolic compounds due to their high antioxidant capacity, have an important role in health and increase the antioxidant defense against oxidative stress. The aim of this study was to evaluate the effect of aqueous extract of white tea on status of antioxidant enzymes (SOD, CAT and GPx), MDA (malondialdehyde) and TAC (total antioxidant capacity) in rats treated with sodium arsenite. In this study, 32 adult male rats weighing 200-250 g were used in four groups of eight. The first group included healthy normal rats (control group), the second group of rats were treated with sodium arsenite (100 ppm in drinking water) the third group of rats were treated with aqueous extract of white tea at a concentration of 1/5%, via gavage, the fourth group of rats were treated with aqueous extract of white tea (1/5%) via gavage with sodium arsenite (100 ppm in drinking water). The rats were killed at the end of the 28th day of treatment and blood samples were collected and the antioxidant enzymes of CAT (catalase), SOD (superoxide dismutase), GPx (glutathione peroxidase), and MDA and TAC were measured. The results indicate that the aqueous extract of white tea significantly increased the activities of SOD, GPx, CAT and TAC and decreased MDA concentration (p<0.05). The results showed consummation of white tea decreased the oxidative stress of arsenic by increasing the activity of antioxidant enzymes and potentiation of antioxidant defense system.
References:
· Aebi, H. (1984). Catalase in vitro. Methods in Enzymology, 105: 121-126.
· Abolfathi, A.A., Mohajeri, D., Rezaie, A. and Nazeri, M. (2012). Protective effects of green tea extract against hepatic tissue injury in streptozotocin-induced diabetic rats. Evidence-Based Complementary and Alternative Medicine 2012.
· Ahlam, A.M., Al-Shiekh, A., Al-Shati, M.B., Mohammed, A.A. and Sarhan, F.M. (2014). Effect of white tea extract on antioxidant enzyme activities of streptozotocin–induced diabetic rats, 30(5): 270-275.
· Almajano, M., Vila, I. and Ginés, S. (2011). Neuro-protective effects of white tea against oxidative stress-induced toxicity in striatal cells. Neurotoxicity Research, 20(4): 372-378.
· Anderson, R.A. and Polansky, M.M. (2002). Tea enhances insulin activity. Journal of Agricultural and Food Chemistry, 50(24): 7182-7186.
· Azram, S., Hadi, N., Khan, N. and Hadi, S. (2004). Pro-oxidant property of green tea polyphenols, epicatechin and epicatechin-3-gallate: implications of anticancer properties. Toxicology, In Vitro, 18: 555-561.
· Celik, I.L., Gallicchio, K., Boyd, T.K., Lam, G. and Tao, X. (2008). Arsenic in drinking water and lung cancer: a systematic review. Environmental Research, 108(1): 48-55.
· Chou, C.C., Lin, L.L. and Chung, K.T. (1999). Antimicrobial activity of tea as affected by the degree of fermentation and manufacturing season. International Journal of Food Microbiology, 48(2): 125-130.
· Ghosh, D.S., Ghosh, S., Sarkar, A., Ghosh, N. and Das Saha, k. (2010). Quercetin in vesicular delivery systems: evaluation in combating arsenic-induced acute liver toxicity associated gene expression in rat model. Chemico- Biological Interactions, 186(1): 61-7.
· Jain, A., Shimoi, K., Nakamura, Y., Kada, T. and Hara, Y. (1989). Crude tea extracts decrease the mutagenic activity of N-methyl-N-nitro-N-nitrosoguanidine in vitro and in intra-gastric tract of rats. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 210(1): 1-8.
Katiyar, S.K., Agarwal, R., Zaim, M.T. and Mukhtar, H. (1993). Protection against N-nitrosodiethylamine and benzo[a] pyrene-induced forestomach and lung tumorigenesis in A/J mice by green tea. Carcinogenesis, 14(5): 849-855.
· Lapenna, D., Ciofani, G., Pierdomenico, S.D., Giamberardino, M.A. and Cuccurullo, F. (2001). Reaction conditions affecting the relationship between thiobarbituric acid reactivity and lipid peroxides in human plasma. Free Radical Biology and Medicine, 31(3): 331-335.
· Mandelker, L. and Vajdovich, P. (2011). Studies on veterinary medicine. Humana press, 2(5): 192-197.
· Martinez, V.D., Vucic, M., Adonis, L. and Lam W.L. (2011). Arsenic biotransformation as a cancer promoting factor by inducing DNA damage and disruption of repair mechanisms. Molecular Biology International, 5(9): 365-373.
· Maron, D.J., Cai, N.S., Wu, Z.G. and Li, Y.H. (2003). Cholesterol-lowering effect of a theaflavin-enriched green tea extract: a randomized controlled trial. Archives of Internal Medicine, 163(12): 1448.
· McCord, J.M. and Fridovich, I. (1969). Superoxide dismutase. An enzymatic function for erythrocuprein (hemocuprein). The Journal of Biological Chemistry, 244(22): 6049-6055.
Mukhtar, H. and Ahmad, N. (1999). Cancer chemoprevention: future holds in multiple agents. Toxicology and Applied Pharmacology, 158(3): 207-210.
· Nakagawa, T. and Yokozawa, T. (2002). Direct scavenging of nitric oxide and superoxide by green tea. Food and Chemical Toxicology, 40(12): 1745-1750.
· Ortsäter, H., Grankvist, N., Wolfram, S., Kuehn, N. and Sjöholm, A. (2012). Diet supplementation with green tea extract epigallocatechin gallate prevents progression to glucose intolerance in db/db mice. Nutrition and Metabolism, 9(1): 11.
· Paglia, D.E. and Valentine, W.N. (1967). Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. Journal of Laboratory and Clinical Medicine, 70(1): 158-169.
Rietveld, A. and Wiseman, S. (2003). Antioxidant effects of tea: evidence from human clinical trials. The Journal of nutrition, 133(10): 3285S-3292S.
· Sano, M., Suzuki, M., Miyase, T., Yoshino, K. and Maeda-Yamamoto M. (1999). Novel anti-allergic catechin derivatives isolated from oolong tea. Journal of Agricultural and Food Chemistry, 47(5): 1906-1910.
· Santana-Rios, G., Orner, G.A., Amantana, A. and Provost, C. (2001). Potent antimutagenic activity of white tea in comparison with green tea in the Salmonella assay. Mutation Research-Genetic Toxicology and Environmental Mutagenesis, 495(1): 61-74.
· Skryzdlewska, E., Ostrowska, J., Stankiewicz, A. and Fabisszewski, R. (2002). Green tea as a potent antioxidant in alcohol intoxication. Addiction Biology, 7: 307-314.
· Vijaya Bhaskar Reddy, M., Sudheer, P., Sasikala, P., Sreenivasula Reddy, S., Hemadri Reddy, A., et al. (2011). Effect of trans-placental and lactational exposure to arsenic on male reproduction in mice. Journal of Reproduction and Infertility, 2(3): 41-45.
· Vinson, J.A., Dabbagh, Y.A., Serry, M.M. and Jang, J. (1995). Plant flavonoids, especially tea flavonols, are powerful antioxidants using an in vitro oxidation model for heart disease. Journal of Agricultural and Food Chemistry, 43(11): 2800.
· Weber, J.M., Ruzindana-Umunyana, A., Imbeault, L. and Sircar, S. (2003). Inhibition of adenovirus infection and adenain by green tea catechins. Antiviral Research, 58(2): 167-173.
· Yen, G.C., Chen, H.Y. and Peng, H.H. (1997). Antioxidant and pro-oxidant effects of various tea extracts. Journal of Agricultural and Food Chemistry, 45(1): 30-34.
· Yoshino, K., Tomita, I., Sano, M., Oguni, I. and Hara, Y. (1994). Effects of long-term dietary supplement of tea polyphenols on lipid peroxide levels in rats. Age, 17(3): 79-85.