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孕中期人羊水细胞培养物无法将C19类固醇芳香化。

Inability of second trimester human amniotic fluid cell cultures to aromatize C19-steroids.

作者信息

O'Shannessy D J, Renwick A G

出版信息

J Inherit Metab Dis. 1985;8(1):25-32. doi: 10.1007/BF01805481.

Abstract

Amniotic fluid (AF) and fibroblast (F) cell types, derived from human amniotic fluid by amniocentesis in the second trimester, were cultured using media of varying composition and their ability to transform C19-steroids to oestrogens was investigated by fluorimetry, radioimmunoassay, tritium release and measurement of cytochrome P450. Although the cells were shown to be metabolically active by the presence of mitotic figures, the incorporation of tritiated leucine into protein and the production of the beta-subunit of hCG, no evidence of aromatization was obtained despite the inclusion in the medium of a number of steroids known to be transformed to oestrogens in several in vivo and in vitro preparations. The addition of reported stimulants of aromatase activity, viz. hCG, FSH, diethylstilbestrol, prostaglandins E2 and F2 alpha and dibutyryl cyclic AMP, was without effect.

摘要

通过妊娠中期羊膜穿刺术从人羊水获得的羊水(AF)和成纤维细胞(F)细胞类型,使用不同成分的培养基进行培养,并通过荧光测定法、放射免疫测定法、氚释放以及细胞色素P450的测量来研究它们将C19 - 类固醇转化为雌激素的能力。尽管通过有丝分裂图的存在、将氚标记的亮氨酸掺入蛋白质以及人绒毛膜促性腺激素β亚基的产生表明细胞具有代谢活性,但尽管在培养基中加入了许多已知在几种体内和体外制剂中可转化为雌激素的类固醇,仍未获得芳香化的证据。添加已报道的芳香化酶活性刺激剂,即人绒毛膜促性腺激素、促卵泡激素、己烯雌酚、前列腺素E2和F2α以及二丁酰环磷酸腺苷,均无效果。

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