Institute of Animal Molecular Biotechnology and Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Institute of Animal Molecular Biotechnology and Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Environ Pollut. 2020 Aug;263(Pt A):114573. doi: 10.1016/j.envpol.2020.114573. Epub 2020 Apr 18.
Epidemiological relationships between pesticide use and male infertility have been suggested for a long time. Etoxazole (ETX), an oxazoline pesticide, has been extensively used for pest eradication. It is considered relatively safe and has low mammalian toxicity because it specifically inhibits chitin synthesis. However, ETX may have toxic effects on the reproductive system. In this study, we examined the effects of ETX on the reproductive system using mouse testis cell lines (TM3 for Leydig cells and TM4 for Sertoli cells) and C57BL/6 male mice. We confirmed that ETX has anti-proliferative effects on the TM3 and TM4 cell lines. Moreover, ETX induced mitochondrial dysfunction and hampers calcium homeostasis. Western blot analysis of MAPK and Akt signaling cascades was performed to demonstrate the mode of action of ETX at a molecular level. Moreover, ETX induced misregulation of genes related to testicular function. Upon oral administration of ETX in C57BL/6 male mice, testis weight was reduced and transcriptional expression related to testis function was altered. These results indicate that ETX induces testicular toxicity by inducing mitochondrial dysfunction and calcium imbalance and regulating gene expression.
长期以来,人们一直认为农药的使用与男性不育之间存在流行病学关系。乙氧唑(ETX)是一种恶唑啉类农药,被广泛用于消灭害虫。由于其特异性抑制几丁质合成,因此被认为相对安全且对哺乳动物毒性低。然而,ETX 可能对生殖系统有毒性作用。在这项研究中,我们使用小鼠睾丸细胞系(TM3 用于间质细胞,TM4 用于支持细胞)和 C57BL/6 雄性小鼠研究了 ETX 对生殖系统的影响。我们证实 ETX 对 TM3 和 TM4 细胞系具有抗增殖作用。此外,ETX 诱导线粒体功能障碍并干扰钙稳态。进行 MAPK 和 Akt 信号通路的 Western blot 分析,以从分子水平上证明 ETX 的作用模式。此外,ETX 诱导与睾丸功能相关的基因失调。在 C57BL/6 雄性小鼠中口服 ETX 后,睾丸重量减轻,与睾丸功能相关的转录表达发生改变。这些结果表明,ETX 通过诱导线粒体功能障碍和钙失衡以及调节基因表达来诱导睾丸毒性。