Methoxychlor and its metabolite HPTE inhibit rat neurosteroidogenic 3α-hydroxysteroid dehydrogenase and retinol dehydrogenase 2

被引:4
作者
Mao, Baiping [1 ,2 ]
Wu, Chengyun [3 ,4 ]
Zheng, Wenwen [1 ,2 ]
Shen, Qiuxia [1 ,2 ]
Wang, Yiyan [1 ,2 ]
Wang, Qiufan [1 ,2 ]
Lin, Han [1 ,2 ]
Li, Xiaoheng [1 ,2 ]
Sun, Jianliang [5 ]
Ge, Ren-Shan [1 ,2 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Anesthesiol, Wenzhou 325027, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 2, Dept Resp Med, Wenzhou, Peoples R China
[4] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Peoples R China
[5] Zhejiang Univ, Sch Med, Hangzhou Peoples Hosp 1, Hangzhou Hosp,Dept Anesthesia, Hangzhou 310006, Zhejiang, Peoples R China
关键词
Methoxychlor; HPTE; Neurosteroid; 3 alpha-Hydroxysteroid dehydrogenase; Retinol dehydrogenase 2; 3-BETA-HYDROXYSTEROID DEHYDROGENASE; 11-BETA-HYDROXYSTEROID DEHYDROGENASE; DIHYDRODIOL DEHYDROGENASE; PESTICIDE METHOXYCHLOR; LEYDIG-CELLS; IN-VITRO; EXPRESSION; MOUSE; 2,2-BIS(P-HYDROXYPHENYL)-1,1,1-TRICHLOROETHANE; TESTOSTERONE;
D O I
10.1016/j.neulet.2018.08.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Methoxychlor is primarily used as an insecticide and it is widely present in the environment. The objective of the present study was to investigate the direct effects of methoxychlor and its metabolite hydroxychlor (HPTE) on rat neurosteroidogenic 3 alpha-hydroxysteroid dehydrogenase (AKR1C14) and retinol dehydrogenase 2 (RDH2) activities. Rat AKR1C14 and RDH2 were cloned and expressed in COS-1 cells, and the effects of methoxychlor and HPTE on these enzymes were measured. HPTE was more potent to inhibit AKR1C14 and RDH2 activities than methoxychlor, with IC50 values of 2.602 +/- 0.057 mu M and 20.473 +/- 0.049 mu M, respectively, while those of methoxychlor were over 100 mu M. HPTE competitively inhibited AKR1C14 and RDH2 when steroid substrates were used, while it showed a mode of mixed inhibition on these enzymes when NADPH/NAD(+) were used. We elucidated the binding mode of methoxychlor and HPTE to the crystal structure of AKR1C14 by molecular docking and found that HPTE had higher affinity with the enzyme than methoxychlor. In conclusion, HPTE is more potent than methoxychlor to inhibit both AKR1C14 and RDH2.
引用
收藏
页码:169 / 174
页数:6
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