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Volume 19, Issue 6 (November 2017) 19, 672–679; 10.4103/1008-682X.192637

Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms

Ozlem Atli1, Merve Baysal1, Gozde Aydogan-Kilic2, Volkan Kilic2, Seyda Ucarcan2, Burak Karaduman1, Sinem Ilgin1

1 Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Anadolu University, Eskisehir 26470, Turkey
2 Department of Biology, Faculty of Science, Anadolu University, Eskisehir 26470, Turkey

Correspondence: Dr. O Atli (oatli@anadolu.edu.tr)

Date of Submission 28-Mar-2016 Date of Decision 24-May-2016 Date of Acceptance 11-Oct-2016 Date of Web Publication 13-Dec-2016


This study was conducted to clarify the toxic effects of sertraline (SRT) on the reproductive system of male rats and to elucidate the underlying mechanisms. Rats were treated orally with SRT at doses of 5, 10, and 20 mg kg−1 for 28 consecutive days. At the end of the treatment period, sperm concentration, sperm motility, and sperm morphology were investigated by computer-assisted sperm analysis system whereas sperm DNA damage was detected by comet assay. The oxidative status of the testes was investigated, and a histopathological examination was conducted. Serum testosterone, follicle-stimulating hormone (FSH), and luteinizing hormone (LH) levels were measured to determine the effects of SRT on the spermatogenesis process. One-way ANOVA, post-hoc Dunnett's T3 test for the sperm comet assay, and post-hoc Tukey's test for the others were performed for statistical analysis. The results showed that SRT caused an increase in sperm DNA damage and induced histopathological lesions in all groups treated with SRT. There was abnormal sperm morphology and increased malondialdehyde (MDA) in the 10 mg kg−1 treatment group. More dramatic changes were observed in the 20 mg kg−1 treatment group. Decreased sperm count was accompanied by a significant increase in abnormal sperm morphology, DNA damage, and degeneration in cellular-tubular structures. Serum LH and testosterone levels were elevated in the 20 mg kg−1 treatment group. Decreased glutathione (GSH) and increased MDA were signs of enhanced oxidative stress (OS). In conclusion, SRT induced testicular toxicity in a dose-dependent manner and OS is suggested as a crucial mechanism.

Keywords: DNA damage; oxidative stress; reproductive toxicity; sertraline

Keywords: DNA damage; oxidative stress; reproductive toxicity; sertraline

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