Department of Clinical Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University , Yangling, China.
Key Laboratory of Animal Biotechnology of the Ministry of Agriculture, Northwest A&F University , Yangling, China.
J Toxicol Environ Health A. 2021 Feb 1;84(3):112-124. doi: 10.1080/15287394.2020.1841699. Epub 2020 Nov 4.
Zearalenone (ZEA), a mycotoxin, is known to impair reproductive capability by disrupting the synthesis and secretion of testosterone by Leydig cells (LCs), although the mechanism is unknown. Robust rhythmicity of circadian clock and steroidogenic genes were identified in LCs. The aim of this study was to examine whether ZEA significantly attenuated the transcription of core clock genes (, and ) as well as steroidogenic genes (, and ) in mouse testis Leydig cell line (TM3). Western blotting confirmed declines in BMAL1, NR1D1, and StAR protein levels. ZEA also suppressed secreted testosterone levels. In primary LCs, isolated from PER2::LUCIFERASE reporter gene knock in mice, ZEA diminished the amplitude of expression, and induced a phase shift and period extension. In primary LCs, ZEA also suppressed the expression levels of core clock and steroidogenic genes, reduced protein levels of BMAL1, and decreased testosterone secretion. expression of core clock and steroidogenic genes were reduced in testes of mice exposed to ZEA for 1 week leading to decreased serum testosterone levels. In summary, data suggest that ZEA may impair testosterone synthesis through attenuation of the circadian clock in LCs culminating in reproductive dysfunction in male mammals .
玉米赤霉烯酮(ZEA)是一种真菌毒素,已知通过破坏睾丸间质细胞(LCs)中睾丸酮的合成和分泌来损害生殖能力,但具体机制尚不清楚。LCs 中存在节律性很强的生物钟和类固醇生成基因。本研究旨在研究 ZEA 是否会显著减弱小鼠睾丸间质细胞瘤系(TM3)中核心时钟基因(,和)以及类固醇生成基因(,和)的转录。Western blot 证实 BMAL1、NR1D1 和 StAR 蛋白水平下降。ZEA 还抑制了分泌型睾丸酮水平。在 PER2::LUCIFERASE 报告基因敲入小鼠分离的原代 LCs 中,ZEA 减弱了表达的振幅,并诱导相位偏移和周期延长。在原代 LCs 中,ZEA 还抑制了核心时钟和类固醇生成基因的表达水平,降低了 BMAL1 蛋白水平,并减少了睾丸酮的分泌。暴露于 ZEA 1 周的小鼠睾丸中核心时钟和类固醇生成基因的表达减少,导致血清睾丸酮水平降低。总之,数据表明 ZEA 可能通过减弱 LCs 中的生物钟来损害睾丸酮的合成,从而导致雄性哺乳动物生殖功能障碍。