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体外培养的猪卵巢卵泡细胞分泌雌二醇-17β和雄激素的研究

Estradiol-17 beta and androgen secretion by isolated porcine ovarian follicular cells in vitro.

作者信息

Tsang B K, Moon Y S, Armstrong D T

出版信息

Can J Physiol Pharmacol. 1982 Aug;60(8):1112-8. doi: 10.1139/y82-160.

Abstract

The cellular sources and gonadotropic regulation of porcine ovarian estrogen and androgen were assessed by culturing isolated granulosa cells and thecal cells from medium size follicles (4-6 mm diameter) separately for 24 h in a chemically defined medium containing gonadotropins and (or) testosterone. At the end of the culture period, estradiol-17 beta (estradiol) and androgens in the media were determined by radioimmunoassays. Production of estradiol by granulosa cells without an exogenous aromatizable androgen was low in the absence or presence of a highly purified preparation of either follicle-stimulating hormone (FSH. 0.25 microgram/mL) or luteinizing hormone (LH. 1 microgram/mL). Addition of testosterone or androstenedione (0.5 microM), but not dihydrotestosterone or pregnenolone, significantly increased estradiol secretion. Additional increases were observed when FSH, LH, prostaglandin E2, or dibutyryl cyclic 3'.5'-adenosine monophosphate was present. Production of estradiol by thecal cells was low in the presence or absence of exogenous testosterone, and was essentially unaffected by the presence of gonadotropins. Thecal cells, however, released large amounts of androstenedione and smaller amounts of testosterone and other androgens during 24-h culture and the production of these androgens was stimulated by LH but not by FSH. Androgen secretion by granulosa cells was negligible when compared with the theca and was unaffected by gonadotropins. It is concluded that the theca is the prime site for follicular androgen biosynthesis by the porcine ovarian follicle, and, upon LH stimulation, may provide androgen precursors for estradiol production by granulosa cells.

摘要

通过在含有促性腺激素和(或)睾酮的化学限定培养基中分别培养来自中等大小卵泡(直径4 - 6毫米)的分离颗粒细胞和卵泡膜细胞24小时,评估了猪卵巢雌激素和雄激素的细胞来源及促性腺激素调节。培养期结束时,通过放射免疫测定法测定培养基中的雌二醇 - 17β(雌二醇)和雄激素。在不存在或存在高度纯化的促卵泡激素(FSH,0.25微克/毫升)或促黄体生成素(LH,1微克/毫升)制剂的情况下,无外源性可芳香化雄激素时颗粒细胞产生的雌二醇水平较低。添加睾酮或雄烯二酮(0.5微摩尔),而非双氢睾酮或孕烯醇酮,可显著增加雌二醇分泌。当存在FSH、LH、前列腺素E2或二丁酰环磷腺苷时,观察到进一步增加。在存在或不存在外源性睾酮的情况下,卵泡膜细胞产生的雌二醇水平较低,并且基本上不受促性腺激素存在的影响。然而,卵泡膜细胞在24小时培养期间释放大量雄烯二酮以及少量睾酮和其他雄激素,并且这些雄激素的产生受到LH而非FSH的刺激。与卵泡膜相比,颗粒细胞的雄激素分泌可忽略不计,并且不受促性腺激素的影响。结论是,卵泡膜是猪卵巢卵泡中卵泡雄激素生物合成的主要部位,并且在LH刺激下,可能为颗粒细胞产生雌二醇提供雄激素前体。

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