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褪黑素对六价铬诱导的精原细胞潜在的双重保护作用。

Potential dual protective effects of melatonin on spermatogonia against hexavalent chromium.

机构信息

Key Laboratory for Animal Genetics, Breeding and Reproduction of Shaanxi Province, College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, China.

College of Veterinary Medicine, Shaanxi Stem Cell Engineering and Technology Center, Northwest A&F University, Yangling, Shaanxi 712100, China.

出版信息

Reprod Toxicol. 2022 Aug;111:92-105. doi: 10.1016/j.reprotox.2022.05.009. Epub 2022 May 26.

DOI:10.1016/j.reprotox.2022.05.009
PMID:35643323
Abstract

Hexavalent chromium (Cr (VI)) is a widely used metal and has been shown to cause male reproductive abnormalities. However, the underlying mechanisms for the Cr (VI)-induced reproductive toxicity remain incompletely understood. In this study, we investigated the spermatogonial damage caused by Cr (VI) as well as the protective effect of melatonin against Cr (VI)-triggered toxicity. We observed that Cr (VI) caused spermatogonial damage in a time- and dose-dependent manner. Results further showed that melatonin could protect spermatogonia from Cr (VI)-triggered damage via elimination of reactive oxygen species (ROS) as well as via suppression of ATM-p53 phosphorylation and the mitogen-activated protein kinase (MAPK) pathway. Prior administration of melatonin also prevented the Cr (VI)-caused enrichment of H3K9me3 in the Mad1, Mad2 and Bcl2 gene promoter regions, precluding the G/M arrest and apoptosis in spermatogonia. Taken together, this study demonstrates that melatonin can effectively protect spermatogonia against the damage and against the histone modification changes induced by Cr (VI). This, along with the uncovered molecular mechanism, provide important implications for male infertility induced by environmental pollution.

摘要

六价铬(Cr(VI))是一种广泛使用的金属,已被证明会导致男性生殖异常。然而,Cr(VI) 引起的生殖毒性的潜在机制仍不完全清楚。在这项研究中,我们研究了 Cr(VI) 引起的精原细胞损伤以及褪黑素对 Cr(VI)触发毒性的保护作用。我们观察到 Cr(VI) 以时间和剂量依赖的方式引起精原细胞损伤。结果进一步表明,褪黑素可以通过消除活性氧 (ROS) 以及抑制 ATM-p53 磷酸化和丝裂原活化蛋白激酶 (MAPK) 途径来保护精原细胞免受 Cr(VI) 引发的损伤。褪黑素的预先给药还可以防止 Cr(VI) 引起 Mad1、Mad2 和 Bcl2 基因启动子区域 H3K9me3 的富集,从而阻止精原细胞的 G/M 阻滞和凋亡。总之,这项研究表明,褪黑素可以有效地保护精原细胞免受 Cr(VI) 引起的损伤和组蛋白修饰变化的影响。这一发现及其揭示的分子机制为环境污染引起的男性不育提供了重要的启示。

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