CTL公司*
精子
促黄体激素
生殖系统
氧化应激
睾酮(贴片)
精子活力
内科学
男科
内分泌学
激素
DNA损伤
生物
生殖毒性
毒性
医学
免疫学
免疫系统
CD8型
DNA
遗传学
作者
Sinem Ilgın,Gözde Kılıç,Merve Baysal,Volkan Kılıç,Büşra Korkut,Şeyda Uçarcan,Özlem Atlı
出处
期刊:Teratology
[Wiley]
日期:2017-03-31
卷期号:109 (7): 475-485
被引量:25
摘要
Background Citalopram hydrobromide (CTL) has been shown to cause sexual dysfunction; however, its reproductive toxicity potential has not been sufficiently elucidated in men. Therefore, we aimed to clarify the toxic effects of CTL on the reproductive system of male rats. Methods For this purpose, CTL was administered at 5, 10, and 20 mg/kg/day to rats orally for 28 days. Sperm concentration, motility, and morphology were investigated using a computer‐assisted sperm analysis system, and sperm DNA damage was detected using a Comet assay. The testes were histopathologically examined. Serum follicle‐stimulating hormone, luteinizing hormone, and testosterone levels were measured and the oxidative status of testes was investigated. Results Our results showed that sperm concentration was reduced, and abnormal sperm morphology and sperm DNA damage were increased in CTL‐administered groups. Additionally, histopathological changes were observed in the testes of CTL‐administered rats. Luteinizing hormone levels were increased in CTL‐administered groups, while testosterone levels were increased in the 5 and 10 mg/kg CTL‐administered groups. Decreased glutathione signaled enhanced oxidative stress in the 10 and 20 mg/kg CTL‐administered groups. Conclusion Thus, we concluded that CT induced testicular damage in male rats; this testicular damage was accompanied by oxidative stress and hormonal changes, which are considered as the important causes of reproductive disorders. Birth Defects Research 109:475–485, 2017. © 2017 Wiley Periodicals, Inc.
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