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西酞普兰诱导雄性大鼠生殖毒性。

Citalopram Induces Reproductive Toxicity in Male Rats.

机构信息

Anadolu University, Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Eskisehir, Turkey.

Anadolu University, Faculty of Science, Department of Biology, Eskisehir, Turkey.

出版信息

Birth Defects Res. 2017 Apr 17;109(7):475-485. doi: 10.1002/bdr2.1010. Epub 2017 Mar 31.

Abstract

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.

摘要

背景

氢溴酸西酞普兰(CTL)已被证明会引起性功能障碍;然而,其在男性中的生殖毒性潜力尚未得到充分阐明。因此,我们旨在阐明 CTL 对雄性大鼠生殖系统的毒性作用。

方法

为此,我们将 CTL 以 5、10 和 20mg/kg/天的剂量通过口服方式给予大鼠 28 天。使用计算机辅助精子分析系统检测精子浓度、活力和形态,使用 Comet assay 检测精子 DNA 损伤。对睾丸进行组织病理学检查。测量血清卵泡刺激素、黄体生成素和睾酮水平,并研究睾丸的氧化状态。

结果

我们的结果表明,CTL 给药组的精子浓度降低,畸形精子形态和精子 DNA 损伤增加。此外,CTL 给药组大鼠的睾丸出现了组织病理学变化。CTL 给药组的黄体生成素水平升高,而 5 和 10mg/kg CTL 给药组的睾酮水平升高。谷胱甘肽减少表明 10 和 20mg/kg CTL 给药组的氧化应激增强。

结论

因此,我们得出结论,CTL 诱导雄性大鼠睾丸损伤;这种睾丸损伤伴随着氧化应激和激素变化,这被认为是生殖障碍的重要原因。出生缺陷研究 109:475-485,2017. © 2017 威利父子出版公司

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