Department of Anesthesiology, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, 325003, China.
Department of Pharmacy, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, 325003, China.
Chemosphere. 2020 Apr;245:125597. doi: 10.1016/j.chemosphere.2019.125597. Epub 2019 Dec 10.
Acephate is an organophosphate pesticide. It is widely used. However, whether it inhibits androgen synthesis and metabolism remains unclear. In the current study, we investigated the effect of acephate on the inhibition of androgen synthetic and metabolic pathways in rat immature Leydig cells after 3-h culture. Acephate inhibited basal androgen output in a dose-dependent manner with the inhibition starting at 0.5 μM. It significantly inhibited luteinizing hormone and 8-Br-cAMP stimulated androgen output at 50 μM. It significantly inhibited progesterone-mediated androgen output at 50 μM. Further study demonstrated that acephate down-regulated the expression of Hsd3b1 and its protein at ≥ 0.5 μM, Lhcgr at 5 μM and Star at 50 μM. Acephate directly blocked rat testicular HSD3B1 activity at 50 μM. Acephate did not affect other androgen synthetic and metabolic enzyme activities as well as ROS production, proliferation, and apoptosis of immature Leydig cells. In conclusion, acephate targets LHCGR, STAR, and HSD3B1, thus blocking androgen synthesis in rat immature Leydig cells and HSD3B1 is being the most sensitive target of acephate.
乙酰甲胺磷是一种有机磷农药。它被广泛使用。然而,它是否抑制雄激素的合成和代谢仍不清楚。在本研究中,我们研究了乙酰甲胺磷在 3 小时培养后对大鼠未成熟莱迪希细胞雄激素合成和代谢途径的抑制作用。乙酰甲胺磷以剂量依赖的方式抑制基础雄激素的产生,抑制作用从 0.5 μM 开始。它在 50 μM 时显著抑制黄体生成素和 8-Br-cAMP 刺激的雄激素产生。它在 50 μM 时显著抑制孕酮介导的雄激素产生。进一步的研究表明,乙酰甲胺磷在≥0.5 μM 时下调 Hsd3b1 及其蛋白的表达,在 5 μM 时下调 Lhcgr 的表达,在 50 μM 时下调 Star 的表达。乙酰甲胺磷在 50 μM 时直接阻断大鼠睾丸 HSD3B1 的活性。乙酰甲胺磷不影响其他雄激素合成和代谢酶的活性以及未成熟莱迪希细胞的 ROS 产生、增殖和凋亡。总之,乙酰甲胺磷靶向 LHCGR、STAR 和 HSD3B1,从而阻断大鼠未成熟莱迪希细胞中的雄激素合成,HSD3B1 是乙酰甲胺磷最敏感的靶标。