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人胎盘中6-羟基孕酮的形成及其对人绒毛膜促性腺激素的反应。

Formation of 6-hydroxylated progesterone in the human placenta and response to hCG.

作者信息

Tabei T, Troen P

出版信息

J Clin Endocrinol Metab. 1975 Apr;40(4):697-704. doi: 10.1210/jcem-40-4-697.

Abstract

The in vitro metabolism of 7alpha-3-H-pregnenolone by five term human placentas obtained from repeat cesarean section was studied. Incubations were carried out either with minced tissue for 1 h or by organ culture for 6 h and 24 h. Twenty-one experiments were performed to determine the effect of human chorionic gonadotropin (hCG), human placental lactogen (hPL), and heat-inactivated hCG on the metabolism of pregnenolone. The major radioactive product was progesterone (40-60%); unchanged pregnenolone accounted for only 5-15% of the radioactivity. 3-H-6beta-OH-progesterone was found and rigorously identified. In control experiments 6beta-OH-progesterone was 2-4% of the radioactivity. In the presence of hCG there was a significant (P smaller than 0.005) 2-3-fold increase of 3-H-6beta-OH-progesterone in the 1-h mince incubations and the 24-h organ cultures. There was no increase of 3-H-6beta-OH-progesterone over control values with hCG after 6-h organ cultures; with heat-inactivated hCG; or with hPL. These findings provide additional data that hCG affects steroid metabolism in the human placenta. In addition, 3-H-6alpha-OH-progesterone was found and rigorously identified in yields of approximately 0.5-1%. The effect of hCG on 6alpha-hydroxylation was not determined. This appears to be the first demonstration of 6alpha-hydroxylation of C21 steroids by human tissue.

摘要

研究了从重复剖宫产获得的五个足月人胎盘对7α-3-H-孕烯醇酮的体外代谢。采用切碎组织孵育1小时或器官培养6小时和24小时的方式进行实验。进行了21项实验,以确定人绒毛膜促性腺激素(hCG)、人胎盘催乳素(hPL)和热灭活hCG对孕烯醇酮代谢的影响。主要放射性产物是孕酮(40%-60%);未变化的孕烯醇酮仅占放射性的5%-15%。发现并严格鉴定了3-H-6β-羟基孕酮。在对照实验中,6β-羟基孕酮占放射性的2%-4%。在hCG存在的情况下,在1小时切碎组织孵育和24小时器官培养中,3-H-6β-羟基孕酮显著增加(P小于0.005),增加了2-3倍。在6小时器官培养后,使用热灭活hCG或hPL时,3-H-6β-羟基孕酮没有超过对照值的增加。这些发现提供了更多数据,表明hCG会影响人胎盘的类固醇代谢。此外,还发现并严格鉴定了3-H-6α-羟基孕酮,产量约为0.5%-1%。未确定hCG对6α-羟基化的影响。这似乎是首次证明人体组织对C21类固醇进行6α-羟基化。

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