Acephate interferes with androgen synthesis in rat immature Leydig cells

被引:14
作者
Wang, Yiyan [1 ,2 ]
Dong, Yaoyao [2 ,3 ]
Wu, Siwen [1 ,2 ]
Zhu, Qiqi [1 ,2 ]
Li, Xiaoheng [1 ,2 ]
Liu, Shiwen [1 ,2 ]
Huang, Tongliang [1 ,2 ]
Li, Huitao [1 ,2 ]
Ge, Ren-Shan [1 ,2 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Anesthesiol, Wenzhou 325003, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325003, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 2, Dept Pharm, Wenzhou 325003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Steroidogenesis; Acephate; Rat immature Leydig cells; Steroidogenic enzymes; Luteinizing hormone receptor; 3 beta-hydroxysteroid dehydrogenase isoform 1; LUTEINIZING-HORMONE RECEPTORS; GENE-EXPRESSION; IN-VIVO; DIFFERENTIATION; DEHYDROGENASE; DIMETHOATE; VITRO; STAR;
D O I
10.1016/j.chemosphere.2019.125597
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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 mu M. It significantly inhibited luteinizing hormone and 8-Br-cAMP stimulated androgen output at 50 mu M. It significantly inhibited progesterone-mediated androgen output at 50 mu M. Further study demonstrated that acephate down-regulated the expression of Hsd3b1 and its protein at >= 0.5 mu M, Lhcgr at 5 mu M and Star at 50 mu M. Acephate directly blocked rat testicular HSD3B1 activity at 50 mu M. 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. (C) 2019 Elsevier Ltd. All rights reserved.
引用
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页数:11
相关论文
共 29 条
  • [11] The (+)- and (-)-gossypols potently inhibit both 3β-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase 3 in human and rat testes
    Hu, Guo-Xin
    Zhou, Hong-Yu
    Li, Xing-Wang
    Chen, Bing-Bing
    Xiao, Ye-Chen
    Lian, Qing-Quan
    Liang, Guang
    Kim, Howard H.
    Zheng, Zhi-Qiang
    Hardy, Dianne O.
    Ge, Ren-Shan
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2009, 115 (1-2) : 14 - 19
  • [12] Jasuja N. D., 2013, African Journal of Pharmacy and Pharmacology, V7, P1554
  • [13] Joshi S. C., 2012, Research Journal of Pharmaceutical, Biological and Chemical Sciences, V3, P137
  • [14] Joshi S. C., 2012, INT J RES PHARM BIOM, V3, P286
  • [15] LePage JT, 2005, J AOAC INT, V88, P1788
  • [16] Effects of Etomidate on the Steroidogenesis of Rat Immature Leydig Cells
    Liu, Hua-Cheng
    Zhu, Danyan
    Wang, Chan
    Guan, Hongguo
    Li, Senlin
    Hu, Cong
    Chen, Zhichuan
    Hu, Yuanyuan
    Lin, Han
    Lian, Qing-Quan
    Ge, Ren-Shan
    [J]. PLOS ONE, 2015, 10 (11):
  • [17] Regulation of the steroidogenic acute regulatory protein gene expression: present and future perspectives
    Manna, Pulak R.
    Dyson, Matthew T.
    Stocco, Douglas M.
    [J]. MOLECULAR HUMAN REPRODUCTION, 2009, 15 (06) : 321 - 333
  • [18] Constitutively active luteinizing hormone receptors:: Consequences of in vivo expression
    Meehan, Thomas P.
    Narayan, Prema
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2007, 260 : 294 - 300
  • [19] PAYNE AH, 1980, J BIOL CHEM, V255, P7118
  • [20] Acephate exposure during a perinatal life program to type 2 diabetes
    Ribeiro, Tatiane Aparecida
    Prates, Kelly Valerio
    Pavanello, Audrei
    Malta, Ananda
    Tofolo, Laize Peron
    Martins, Isabela Peixoto
    de Oliveira, Julio Cezar
    Miranda, Rosiane Aparecida
    Gomes, Rodrigo Mello
    Vieira, Elaine
    da Silva Franco, Claudineia Conationi
    Barella, Luiz Felipe
    Francisco, Flavio Andrade
    Alves, Vander Silva
    Silveira, Sandra da Silva
    Moreira, Veridiana Mota
    Fabricio, Gabriel Sergio
    Palma-Rigo, Kesia
    Sloboda, Deborah M.
    de Freitas Mathias, Paulo Cezar
    [J]. TOXICOLOGY, 2016, 372 : 12 - 21