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J Biomed Biotechnol ; 2012: 362049, 2012.
Article in English | MEDLINE | ID: mdl-22675250

ABSTRACT

The aim of this study was to evaluate the protective effects of Ginkgo biloba (GB) against testicular damage and oxidative stress as well as caudal sperm indices in a cisplatin- (CIS-) induced rodent model. Adult male Wistar rats were given vehicle, single i.p. dose of CIS alone (10 mg/kg), GB alone (200 mg g/kg every day for five days), or single dose of CIS followed by GB (50, 100, or 200 mg/kg every day for five days). On day 6, after the first drug treatment oxidative and apoptotic testicular toxicity was evaluated. CIS-treated rats displayed decreased weights of testes and epididymis as well as caudal sperm count and motility. This reproductive toxicity was accompanied with increased germ-cell degeneration in seminiferous tubules and increased germ-cell apoptosis, increased testicular MDA levels and MPO activity, and decreased SOD and CAT activities in testes. Intensive expressions of COX-2, iNOS, and NF-κB p65 in testicular tissues were detected in CIS-treated group. Oral GB administrations at all doses to CIS-treated rats effectively alleviated all of the CIS-induced toxicity in reproductive system. The present results provide further insights into the mechanisms of protection against CIS-induced reproductive toxicity and confirm the essential antioxidant potential of a GB extract.


Subject(s)
Cisplatin/toxicity , Ginkgo biloba/chemistry , Plant Extracts/pharmacology , Protective Agents/pharmacology , Testis/drug effects , Testis/pathology , Analysis of Variance , Animals , Drug Interactions , Epididymis/drug effects , Immunohistochemistry , In Situ Nick-End Labeling , Male , Organ Size/drug effects , Oxidative Stress/drug effects , Rats , Rats, Wistar , Sperm Motility/drug effects
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