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免疫纯化的促卵泡激素刺激格拉夫卵泡中环状AMP积累和类固醇生成以及诱导大鼠卵子成熟和排卵的能力。

Capacity of immunologically purified FSH to stimulate cyclic AMP accumulation and steroidogenesis in Graafian follicles and to induce ovum maturation and ovulation in the rat.

作者信息

Tsafriri A, Lieberman M E, Koch Y, Bauminger S, Chobsieng P, Zor U, Lindner H R

出版信息

Endocrinology. 1976 Mar;98(3):655-61. doi: 10.1210/endo-98-3-655.

Abstract

Reference preparations of ovine follicle-stimulating hormone (NIH-FSH-S8 and S9; 10-50 mug/ml) induced ovum maturation and stimulated cyclic AMP formation, as well as progesterone and 17beta-estradiol secretion, by rat Graafian follicles in vitro. These actions of NIH-FSH were retained after immunoabsorption of any contaminating luteinizing hormone (LH) present in the preparations, by treatment with an antiserum to the beta-subunit of purified ovine LH (anti-betaLH). In contrast, the corresponding biological actions of NIH-LH-S18 (0.5-10 mug/ml) were abolished by treatment with this anti-betaLH serum. A highly purified FSH preparation (64-96 CD, 0.25 mug/ml) also triggered oocytic meiosis and increased follicular progesterone secretion in vitro. Intraperitoneal (ip) administration of anti-betaLH-treated NIH-FSH-S9 (50 mug/rat at 1430 h) consistently induced ovulation in proestrous rats in which the endogenous gonadotropin surge had been blocked by ip injection of either Nembutal (1345 h) or antiserum to the LH-releasing hormone (1200 h). Injection (ip) of anti-betaLH serum on its own into proestrous rats at 1200 h prevented ovum maturation and follicular rupture. We conclude that currently available reference preparations of ovine FSH possess the capacity to stimulate follicular adenylate cyclase, steroidogenesis, and ovum maturation in vitro, as well as ovulation in vivo, in the rat, and that this capacity cannot be attributed to contamination with material immunochemically identical with LH. However, it is inferred that the physiological triggering of ovulation and related events in this species depends principally on LH.

摘要

绵羊促卵泡激素的标准品(NIH-FSH-S8和S9;10 - 50微克/毫升)可诱导大鼠格拉夫卵泡在体外成熟,并刺激环磷酸腺苷的生成,以及孕酮和17β - 雌二醇的分泌。在用抗纯化绵羊促黄体生成素β亚基抗血清(抗βLH)处理以免疫吸附制剂中存在的任何污染性促黄体生成素(LH)后,NIH-FSH的这些作用得以保留。相比之下,用这种抗βLH血清处理后,NIH-LH-S18(0.5 - 10微克/毫升)相应的生物学作用被消除。一种高度纯化的FSH制剂(64 - 96 CD,0.25微克/毫升)在体外也能触发卵母细胞减数分裂并增加卵泡孕酮分泌。在动情前期大鼠中,内源性促性腺激素高峰已被腹腔注射戊巴比妥(1345小时)或促黄体生成素释放激素抗血清(1200小时)阻断,腹腔注射(ip)经抗βLH处理的NIH-FSH-S9(50微克/只,1430小时)能持续诱导排卵。在1200小时将抗βLH血清单独腹腔注射到动情前期大鼠体内可防止卵子成熟和卵泡破裂。我们得出结论,目前可用的绵羊FSH标准品具有在体外刺激卵泡腺苷酸环化酶、类固醇生成和卵子成熟以及在大鼠体内诱导排卵的能力,并且这种能力不能归因于与LH免疫化学性质相同的物质污染。然而,可以推断该物种排卵及相关事件的生理触发主要取决于LH。

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