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孕烯醇酮和孕酮代谢产物对马胎盘3β-羟基类固醇脱氢酶(3β-HSD)活性的调节作用。

Modulation of 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) activity in the equine placenta by pregnenolone and progesterone metabolites.

作者信息

Chavatte P M, Rossdale P D, Tait A D

机构信息

Department of Paediatrics, University of Cambridge, Addenbrooke's Hospital, UK.

出版信息

Equine Vet J. 1995 Sep;27(5):342-7. doi: 10.1111/j.2042-3306.1995.tb04068.x.

Abstract

The purpose of this study was to measure 3beta-HSD activity in the equine placenta and to assess the effect of fetal and maternal blood plasma progestagens on 3beta-HSD activity was measured in 8 late gestation (collected by caesarian section at 250 to 320 days) and 7 term (collected by caesarian section at 250 to 320 days) and 7 term (collected at birth) equine placentae using a tritium release assay with [3alpha-3H] pregnenolone as substrate. Mean +/- s.d. Km(app) and Vmax for term placentae were in general higher than for late gestation placentae (0.129 +/- 0.217 micromol/l and 23.85 +/- 9.1 nmol/mg/h respectively vs. 0.016 +/- 0.048 micromol/l and 17.36 +/- 20.9 nmol/mg/h) but there was no statistical difference between them. Inhibition studies were performed on 3 term placentae and 3 late gestation ones. Steroid concentrations used for inhibition studies were close to blood plasma concentrations (0.5 to 2 micromol/l). 3beta-hydroxy compounds (5alpha-pregnene-3beta, 20alpha-diol and 3beta-hydroxy-5alpha-pregnan-20-one) showed noncompetitive or mixed inhibition. Mean Ki(app) of 0.7 micromol/l. Inhibition was competitive with 20alpha-hydroxy-5alpha-pregnan-3-one with a mean Ki(app) of 0.1 micromol/l.

摘要

本研究的目的是测定马胎盘组织中3β-羟类固醇脱氢酶(3β-HSD)的活性,并评估胎儿和母体血浆孕激素对其活性的影响。使用以[3α-³H]孕烯醇酮为底物的氚释放试验,对8个妊娠晚期(妊娠250至320天通过剖宫产采集)、7个足月(妊娠250至320天通过剖宫产采集)以及7个足月(出生时采集)的马胎盘组织进行了3β-HSD活性测定。足月胎盘组织的平均±标准差Km(app)和Vmax总体上高于妊娠晚期胎盘组织(分别为0.129±0.217 μmol/L和23.85±9.1 nmol/mg/h,而妊娠晚期胎盘组织分别为0.016±0.048 μmol/L和17.36±20.9 nmol/mg/h),但两者之间无统计学差异。对3个足月胎盘组织和3个妊娠晚期胎盘组织进行了抑制研究。用于抑制研究的类固醇浓度接近血浆浓度(0.5至2 μmol/L)。3β-羟基化合物(5α-孕烯-3β,20α-二醇和3β-羟基-5α-孕烷-20-酮)表现出非竞争性或混合性抑制作用,平均Ki(app)为0.7 μmol/L。20α-羟基-5α-孕烷-3-酮表现出竞争性抑制作用,平均Ki(app)为0.1 μmol/L。

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