Effect of aqueous extract of Asparagus officinalis on some Antioxidants in Rats Exposed to Oxidative Stress induced by Hydrogen peroxide
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Abstract
The current study dealt with using of hydrogen peroxide with 0.5% with drinking water to induce state of oxidative stress in male rats and estimate the ability of different concentrations of the aqueous extract of asparagus officinalis to reduce the effects of oxidative stress during periods 0,15,30 days by measuring the following parameters in serum: Glutathione(GSH), Malondialdehyde (MDA), the activity of super oxide dismutase enzyme (SOD) and the peroxynitrate radical (ONOO).
Fifty male rats with the age of 3-4 months and weight of 300-400 gm were distributed into 5 groups: group (1): control group received drinking tap water, group (2): treated with H2O2 0.5% in drinking water, group (3): treated with H2O2 and asparagus officinalis 5%, group (4): treated with H2O2 and asparagus officinalis 10%, group (5): treated with H2O2 and asparagus officinalis 20% . Hydrogen peroxide treatment led to a significant decrease (P <0.05) of the GSH and SOD activities and increase of the MDA and ONOO levels in the serum during treatment periods compared with the control group. The results of using different concentrations of aqueous extract of asparagus on rats revealed similar effects but not identical in the protection from the oxidative stress induced by Hydrogen Peroxide , because its effect was affected on the level of GSH, SOD, MDA and ONOO levels in the blood serum in different experiment period.
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References
1- Germplasm Resources Information Network, United States Department of Agriculture Agricultural Research Service, Beltsville Area [12 Sep 2012].
2- Al-Snafi, A.E. (2013). Encyclopedia of the constituents and pharmacological effects of Iraqi medicinal plants. Thi qar University.
3- Vinson, J.A.; Hao, Y.; Su, X; Zubik, L.(1998). Phenol antioxidant quantity and quality in foods: vegetables. J Agric Food Chem, 46(9), 3630-3634.
4- Tsushida. T,; Suzuki, M. ;Kurogi M. (1994). Evaluation of antioxidant activity of vegetable extracts and determination of some active compounds. J Jap Soc Food Sci Technol, 41, 1994, 611-618.
5- Maeda, T.; Kakuta, H.; Sonoda, S.; Ueno, R.; Suzuki, T.; Oosawa, K. (2005). Antioxidation capacities of extracts from green, purple, and white asparagus spears related to polyphenol concentration. Hortic Sci, 40, 1221-1224.
6- Pitkin, R.M.(2007). Folate and neural tube defects. The American Journal of Clinical Nutrition 85(1): 285S-288S.
7- Ye, M.; Li, R.; Liao, H.; Liao, X.; Huang, G. (1994). Pharmacological study on Asparagus officinalis Linn. Zhongguo Zhong Yao Za Zhi, 19(4), 240-242.
8- Jang, D.S.; Cuendet, M.; Fong, H.; Pezzuto, J.M.; Kinghorn, A.D. (2004). Constituents of Asparagus officinalis evaluated for inhibitory activity against cyclooxygenase-2. J Agric Food Chem, 52 (8), 2218-2222.
9- Bing, G. and Zongjie, Z.(1994). The protecting effect of asparagus on the rat liver injured by CCl4. Journal of Guiyang Medical College, 19 (1), 10-12.
10- Sakaguchi, Y.; Ozaki, Y.; Miyajima, I.; Yamaguchi, M.; Fukui, Y.; Iwasa, K.; Motoki, S. (2008). Major anthocyanins from purple asparagus (Asparagus officinalis). Phytochemistry, 69(8), 1763-1766.
11- Schilcher, H. and Rau, H. (1988). Nachweis der aquaretischen Wirkung von Birkenblatterund Goldrutenauszugen im Tierversuch. Urologe [B], 28, 274-280.
12- Lu, J.H. (2013). The effects of cooked whole asparagus (Asparagus officinalis L.) and its purified bioactive, rutin, on symptoms of DSS-induced acute colitis and recovery in C57BL/6 mice. MSc thesis, University of Guelph, Guelph, Ontario, Canada.
14- Tietz, N.W. (1999). Textbook of clinical chemistry. 3rd ed. C.A. Burtis, E.R. Ashwood, W.B. Saunders. Pp: 819-861,1245-1250.
15- Brown, M. S. and Goldstein, K. (1983). Ann. Rev. Biochem. 52, 223. Cited by Al Zamely et al., 2001. oxidative stress in prostate cancer patients. MCS. Kufa University College Of Medicine.
16- Beuge, J. A. and Aust, S. D. (1978). Estimation of serum malondialdehyde level. Methods in Enzymology. Academic Press, London, 51: 302.
17- Vanuffelen, B.E.; Van Derzec, J.; Deskoster, B.M.(1998). Biochem. J. 330, 719. Cited by AL-Zamely et al., 2001. The level of malondialdehyde after activation with (H2O2 and CuSO4) and inhibition by Desferoxamine and Molisidomine in serum of patient with acute myocardial infarction. National J. of chemistry, 139-148.
18- Hsu, C. H.; Chi, B. C.; Liu, M. Y. ; Li, J. H. ; Chen, C. J. ; Chen, R. Y. (2002). Phosphine-induced oxidative damage in rats: role of glutathione. Toxicology, 30: 179(1-2): 5-8.
19- Reed, D. J. and Fariss, M. W. (1994). Glutathions depletion and susceptibility. Pharmacol. Reviews, 36: 255-355.
20- Martin, R. N.; Stokes, G. B. ;Masters, C. L. (1985). Regulation of the multiple molecular forms of rat liver glucose-6-Phosphate dehydrogenase by insulin and dietary restriction. Biochem. Biophys. Res. Commun., 127: 136-142.
21- Halliwell, B. and Chirico, S. (1993). lipid peroxidation: Its mechanism, measurement, and signficance. Am. J. Clin. Nutr., 57: 715S-725S.
23- Kwon, K.H. (2005). Dietary rutin, but not its aglycone quercetin, ameliorates dextran sulfate sodium-induced experimental colitis in mice: attenuation of pro-inflammatory gene expression. Biochemical pharmacology. 69(3): 395-406.
24- Demirkol, O.; Adams, C.; Ercal, N. (2004). Biologicallyimportant thiols in various vegetables and fruits. J. Agric. Food Chem. 52: 8151- 8154.
25- Abdou, H. and El Mazoudy, R.(2010). Oxidative damage, hyperlipidemia and histological alterations of cardiac and skeletal muscles induced by different doses of diazinon in female rats. J. Hazard.Mater. 182, 273–278.
26- Anila, L. and Vijayalakshmi, N. (2003). Antioxidant action of flavonoids from Mangifera indica and Emblica officinalis in hypercholesterolemic rats. Food Chemistry, pp.569–574.
28- Kerai, M.; Waterfield, C.; Kenyon, S.; Asker, D.; Timbrell, J. (1999). Reversal of ethanol-induced hepatic Steatosis and lipid peroxidation by taurine:A study in Rats. Alcohol and Alcoholism, 34(4): 529-541.
29- Stenvinkel, P.; Diczfalusg, U.; Lindholm, B.; Heimburger, O. (2004). Phosphelipid plasmalogen, asurrogate marker of oxidative Stress, is associated with increased cardiovascular mortality. Nephrol. Dial. Tranplant., 19(4): 972-976.
30- Opoku, A.; Ndlovu, S.; Terblanche, L.; Hutchings, A.(2007). In vivo hepatoprotective effects of Rhoicissus tridentata subsp. cuneifolia, a traditional Zulu medicinal plant, against CCl –induced acute liver injury in rats. S. Afr. J. Bot., 73: 372-377.
31- Necla, K. T.; Murat, G.; Feti, T.; Gulcin, A. (2005). Peroxynitrite induced decrease in Nat -Kt-ATPase activity is restored by taurine. Biochem. world . J. Gastroenterol., 11(23): 3554-3557.
32- Dukic, N. M. (2003). Antioxidants in health and diseases. Atherosclerosis, 15(2): 423-611.
33- Saikat, S. and Raja, C. (2011). Oxidative Stress: Diagnostics, Prevention and Therapy. American Chemical Society Vol. 1083, 31-37.