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首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Toxic effects of zearalenone and alpha-zearalenol on the regulation of steroidogenesis and testosterone production in mouse Leydig cells.
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Toxic effects of zearalenone and alpha-zearalenol on the regulation of steroidogenesis and testosterone production in mouse Leydig cells.

机译:玉米赤霉烯酮和α-玉米赤霉烯醇对小鼠Leydig细胞中类固醇生成和睾丸激素产生的调节作用。

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摘要

Zearalenone (ZEA) and its derivative alpha-zearalenol (alpha-ZOL) are produced by fungi of the genus Fusarium and, after ingestion via contaminated cereals, may lead to animal fertility disturbances and other reproductive pathologies. The previous study demonstrated the toxic effects of ZEA and alpha-ZOL through disturbances in male fertility and other reproductive pathologies in mice. In this study, we further examined the direct biological effects of ZEA and alpha-ZOL on steroidogenesis production, primarily in Leydig cells of mice. Mature mouse Leydig cells were purified by Percoll gradient centrifugation and the cell purity was determined by 3beta-hydroxysteroid dehydrogenase (3beta-HSD) staining. To examine ZEA and alpha-ZOL-induced biological consequences, we measured testosterone secretion and transcription level of 3 key steroidogenic enzymes including 3beta-HSD-1, P450scc and StAR, in ZEA and alpha-ZOL/human chorionicgonadotropin (hCG) co-treated cells. Our results showed that ZEA and alpha-ZOL (10(-4)M, 10(-6)M and 10(-8)M) significantly suppressed hCG (10ng/ml)-induced testosterone secretion. The suppressive effect is correlated with a decrease in the level of transcription of 3beta-HSD-1, P450scc, and StAR (P<0.05).
机译:玉米赤霉烯酮(ZEA)及其衍生的α-玉米赤霉烯醇(α-ZOL)由镰刀菌属真菌产生,经污染谷物摄入后,可能导致动物繁殖障碍和其他生殖疾病。先前的研究证明了ZEA和α-ZOL通过干扰雄性生育力和小鼠其他生殖病理的毒性作用。在这项研究中,我们进一步检查了ZEA和α-ZOL对类固醇生成的直接生物学效应,主要是在小鼠的Leydig细胞中。通过Percoll梯度离心法纯化成熟的小鼠Leydig细胞,并通过3beta-羟类固醇脱氢酶(3beta-HSD)染色确定细胞纯度。为了检查ZEA和α-ZOL诱导的生物学后果,我们测量了ZEA和联合治疗的α-ZOL/人绒毛膜促性腺激素(hCG)中3种主要的类固醇生成酶(包括3beta-HSD-1,P450scc和StAR)的睾丸激素分泌和转录水平细胞。我们的结果表明ZEA和α-ZOL(10(-4)M,10(-6)M和10(-8)M)显着抑制了hCG(10ng / ml)诱导的睾丸激素分泌。抑制作用与3beta-HSD-1,P450scc和StAR的转录水平降低相关(P <0.05)。

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