Wang Yiyan, Dong Yaoyao, Fang Yinghui, Lv Yao, Zhu Qiqi, Li Xiaoheng, Lian Qingquan, Ge Ren-Shan
Department of Anesthesiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Endocr Connect. 2019 Jul;8(7):1061-1069. doi: 10.1530/EC-19-0288.
Glucocorticoid hormone might cause intrauterine growth restriction. The glucocorticoid-metabolizing enzyme 11β-hydroxysteroid dehydrogenase 2 (HSD11B2) in the placenta eliminates excess levels of glucocorticoids during pregnancy. The aim of the current study was to define the effects of diethylstilbestrol (DES) on HSD11B2 activity in the mammalian placentas and identify its mode of action. Rat and human placental microsomal HSD11B2 were incubated with different concentrations of DES, and IC50 values were determined. The mode of action was analyzed by incubation of DES together with substrates, glucocorticoid and NAD+. DES suppressed rat and human HSD11B2 with IC50 values of 5.33 and 12.62 μM, respectively. DES was a competitive inhibitor of rat and human HSD11B2 when steroid substrates were added, while it was an uncompetitive inhibitor when cofactor NAD+ was exposed. Oral administration of DES (0.5 mg/kg) to the rat delayed the cortisol metabolism in adult female Sprague-Dawley rats, as indicated by the increases in cortisol's elimination half-life, maximum concentration and area under the curve. In conclusion, DES is a potent HSD11B2 inhibitor, possibly contributing to the intrauterine growth restriction.
糖皮质激素可能会导致胎儿宫内生长受限。胎盘中的糖皮质激素代谢酶11β-羟基类固醇脱氢酶2(HSD11B2)在孕期可消除过量的糖皮质激素。本研究的目的是确定己烯雌酚(DES)对哺乳动物胎盘HSD11B2活性的影响,并确定其作用模式。将大鼠和人胎盘微粒体HSD11B2与不同浓度的DES一起孵育,并测定IC50值。通过将DES与底物、糖皮质激素和NAD+一起孵育来分析其作用模式。DES抑制大鼠和人HSD11B2,其IC50值分别为5.33和12.62μM。添加类固醇底物时,DES是大鼠和人HSD11B2的竞争性抑制剂,而当辅因子NAD+存在时,它是非竞争性抑制剂。给大鼠口服DES(0.5mg/kg)会延迟成年雌性Sprague-Dawley大鼠的皮质醇代谢,这表现为皮质醇消除半衰期、最大浓度和曲线下面积增加。总之,DES是一种有效的HSD11B2抑制剂,可能导致胎儿宫内生长受限。