Ameliorative effects of rutin against cisplatin-induced reproductive toxicity in male rats

Springer Science and Business Media LLC - Tập 18 - Trang 1-11 - 2018
Sarwat Jahan1, Asma Munawar1, Suhail Razak1,2, Sara Anam1, Qurat Ul Ain1, Hizb Ullah1, Tayyaba Afsar3, Mahmoud Abulmeaty2, Ali Almajwal2
1Reproductive physiology laboratory, Department of animal sciences, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan
2Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia
3Department of Biochemistry, Faculty of Biological SciencesQuaid-i-Azam University, Islamabad, Pakistan

Tóm tắt

Cisplatin (CP) or cis-diammine dichloroplatinum (II) is a platinum based standard antineoplastic drug which is used against variety of solid tumors and neoplasms. The present study aimed to evaluate the shielding effects of rutin against CP induced testicular toxicity in rats. 28 male rats were divided into four groups. First group was given saline orally while second group received intra-peritoneal (i.p) injection of cisplatin (7 mg/kg) on day first and received saline for next 13 days. Third group received i.p injection of cisplatin at day one and treated with rutin (75 mg/kg) orally for next 13 days. Fourth group was treated with rutin orally for 13 days. Animals were sacrificed on 14th day and reproductive organs were analyzed for various parameters. Cisplatin treatment resulted in a significant decrease in daily sperm production, decrease in head length and % DNA in head, reduction of epithelial cell height, tubular diameter, reduction of the number of spermatogonia, spermatocytes and spermatids, increase in the thiobarbituric acid reactive substances (TBARS) and oxidative stress in testicular tissues, and change of the intra-testicular testosterone concentrations. Rutin co-treatment resulted in reversing cisplatin effect on DNA damage, sperm count, histological and biochemical parameters. These results indicated that rutin co-treatment could ameliorate cisplatin-induced reproductive toxicity in male rats.

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