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

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 concent...

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Main Authors: Ozlem Atli, Merve Baysal, Gozde Aydogan-Kilic, Volkan Kilic, Seyda Ucarcan, Burak Karaduman, Sinem Ilgin
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Asian Journal of Andrology
Subjects:
Online Access:http://www.ajandrology.com/article.asp?issn=1008-682X;year=2017;volume=19;issue=6;spage=672;epage=679;aulast=
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author Ozlem Atli
Merve Baysal
Gozde Aydogan-Kilic
Volkan Kilic
Seyda Ucarcan
Burak Karaduman
Sinem Ilgin
author_facet Ozlem Atli
Merve Baysal
Gozde Aydogan-Kilic
Volkan Kilic
Seyda Ucarcan
Burak Karaduman
Sinem Ilgin
author_sort Ozlem Atli
collection DOAJ
description 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.
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spelling doaj.art-450246ce2bc84af0a0d4e4153c8e8c752022-12-21T17:43:05ZengWolters Kluwer Medknow PublicationsAsian Journal of Andrology1008-682X1745-72622017-01-0119667267910.4103/1008-682X.192637Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanismsOzlem AtliMerve BaysalGozde Aydogan-KilicVolkan KilicSeyda UcarcanBurak KaradumanSinem IlginThis 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.http://www.ajandrology.com/article.asp?issn=1008-682X;year=2017;volume=19;issue=6;spage=672;epage=679;aulast=DNA damage; oxidative stress; reproductive toxicity; sertraline
spellingShingle Ozlem Atli
Merve Baysal
Gozde Aydogan-Kilic
Volkan Kilic
Seyda Ucarcan
Burak Karaduman
Sinem Ilgin
Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
Asian Journal of Andrology
DNA damage; oxidative stress; reproductive toxicity; sertraline
title Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
title_full Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
title_fullStr Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
title_full_unstemmed Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
title_short Sertraline-induced reproductive toxicity in male rats: evaluation of possible underlying mechanisms
title_sort sertraline induced reproductive toxicity in male rats evaluation of possible underlying mechanisms
topic DNA damage; oxidative stress; reproductive toxicity; sertraline
url http://www.ajandrology.com/article.asp?issn=1008-682X;year=2017;volume=19;issue=6;spage=672;epage=679;aulast=
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AT gozdeaydogankilic sertralineinducedreproductivetoxicityinmaleratsevaluationofpossibleunderlyingmechanisms
AT volkankilic sertralineinducedreproductivetoxicityinmaleratsevaluationofpossibleunderlyingmechanisms
AT seydaucarcan sertralineinducedreproductivetoxicityinmaleratsevaluationofpossibleunderlyingmechanisms
AT burakkaraduman sertralineinducedreproductivetoxicityinmaleratsevaluationofpossibleunderlyingmechanisms
AT sinemilgin sertralineinducedreproductivetoxicityinmaleratsevaluationofpossibleunderlyingmechanisms