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性腺甾体3α-羟基-4-孕烯-20-酮对垂体前叶细胞促卵泡激素分泌的选择性抑制作用

Selective suppression of follicle-stimulating hormone secretion in anterior pituitary cells by the gonadal steroid 3 alpha-hydroxy-4-pregnen-20-one.

作者信息

Wood P H, Wiebe J P

机构信息

Department of Zoology, University of Western Ontario, London, Canada.

出版信息

Endocrinology. 1989 Jul;125(1):41-8. doi: 10.1210/endo-125-1-41.

Abstract

The effect of 3 alpha-hydroxy-4-pregnen-20-one (3HP), a Sertoli cell steroid, on the secretion of gonadotropins from rat anterior pituitary cells in culture was examined and subsequently compared with the action of other gonadal steroids and steroids structurally related to 3HP. Pituitary cells from randomly cycling, sexually mature female rats were isolated and maintained in culture 72 h before use. On the day of treatment, medium was changed, steroids (10(-16)-10(-4) M) and/or LHRH (10(-8) M) were added, and cells were allowed to incubate for a further 24 h. Medium was then examined for gonadotropin content by RIA. 3HP treatment of anterior pituitary cells resulted in a significant reduction of both basal and LHRH-induced FSH secretion, while LH secretion was unaffected. The lowest effective dose of 3HP (10(-16) M) significantly decreased basal FSH secretion to 65.6% of control levels. The lowest effective dose of 3HP that significantly inhibited (by 31%) LHRH-induced FSH secretion was 10(-14) M 3HP. Maximum suppression by 3HP of basal FSH secretion occurred between 10(-10)-10(-8) M, and maximum suppression of LHRH-induced secretion occurred at 10(-12) M. None of the other gonadal steroids tested (progesterone, testosterone, 5 alpha-dihydrotestosterone, 17 beta-estradiol, 20 alpha-hydroxy-4-pregnen-3-one, and 5 alpha-pregnane-3,20-dione) had a similar selective effect on FSH secretion; progesterone, testosterone, and 17 beta-estradiol actually resulted in increased FSH release, and 5 alpha-pregnane-3,20-dione resulted in significant increase in basal LH. A number of metabolites and structural variations of 3HP were examined in this in vitro system at concentrations of 10(-12)-10(-6) M, and none exhibited a similar selective FSH-suppressing activity as 3HP. The data suggest that the selective FSH-suppressing effect of 3HP seen previously in vivo and here in vitro is due to 3HP itself and not the result of a metabolite of this molecule.

摘要

研究了支持细胞类固醇3α-羟基-4-孕烯-20-酮(3HP)对培养的大鼠垂体前叶细胞促性腺激素分泌的影响,并随后将其与其他性腺类固醇以及与3HP结构相关的类固醇的作用进行了比较。从随机发情、性成熟的雌性大鼠中分离出垂体细胞,并在使用前在培养中维持72小时。在处理当天,更换培养基,加入类固醇(10⁻¹⁶ - 10⁻⁴ M)和/或促性腺激素释放激素(LHRH,10⁻⁸ M),并使细胞再孵育24小时。然后通过放射免疫分析(RIA)检测培养基中的促性腺激素含量。用3HP处理垂体前叶细胞导致基础和LHRH诱导的促卵泡激素(FSH)分泌均显著降低,而促黄体生成素(LH)分泌未受影响。3HP的最低有效剂量(10⁻¹⁶ M)可使基础FSH分泌显著降低至对照水平的65.6%。显著抑制(31%)LHRH诱导的FSH分泌的3HP最低有效剂量为10⁻¹⁴ M 3HP。3HP对基础FSH分泌的最大抑制作用发生在10⁻¹⁰ - 10⁻⁸ M之间,对LHRH诱导分泌的最大抑制作用发生在10⁻¹² M。所测试的其他性腺类固醇(孕酮、睾酮、5α-二氢睾酮、17β-雌二醇、20α-羟基-4-孕烯-3-酮和5α-孕烷-3,20-二酮)均未对FSH分泌产生类似的选择性作用;孕酮、睾酮和17β-雌二醇实际上导致FSH释放增加,5α-孕烷-3,20-二酮导致基础LH显著增加。在该体外系统中,以10⁻¹² - 10⁻⁶ M的浓度检测了3HP的多种代谢产物和结构变体,没有一种表现出与3HP类似的选择性抑制FSH的活性。数据表明,先前在体内和此处体外观察到的3HP对FSH的选择性抑制作用是由于3HP本身,而不是该分子代谢产物的结果。

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