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多种哺乳动物促性腺激素对培养的大鼠颗粒细胞雌激素和孕酮分泌的影响。

Effect of diverse mammalian gonadotropins on estrogen and progesterone production by cultured rat granulosa cells.

作者信息

Hsueh A J, Erickson G F, Papkoff H

出版信息

Arch Biochem Biophys. 1983 Sep;225(2):505-11. doi: 10.1016/0003-9861(83)90060-7.

Abstract

The ability of gonadotropins from six mammalian species to stimulate estrogen and progesterone production was investigated in granulosa cells of hypophysectomized estrogen-primed immature female rats. Granulosa cells were cultured for 2 days in the presence of delta 4-androstenedione (10(-7) M) with or without various gonadotropin preparations. Treatment with follitropin (follicle-stimulating hormone, FSH) from human, rat, ovine, porcine, equine, and bovine origins resulted in dose-dependent increases in steroidogenesis from negligible amounts to maximal levels of approximately 4-8 and 12-30 ng/10(5) cells for estrogen and progesterone, respectively. The ED50 values of the FSH preparations for stimulation of steroidogenesis were: human: 1-4 ng/ml; ovine: 2.5-30 ng/ml; rat: 1.6-4.0 ng/ml; porcine: 7.5-20 ng/ml; equine 2.5-6 ng/ml; and bovine greater than 100 ng/ml. Lutropin (luteinizing hormone, LH) from rat, ovine, bovine, and porcine origins, human chorionic gonadotropin (hCG), the alpha-subunit of human FSH and the beta-subunit of human LH were ineffective in stimulating steroidogenesis, indicating the specificity of the assay system for FSH. In a high concentration (600 ng/ml), the beta-subunit of human FSH-stimulated steroidogenesis to a small extent. Furthermore, pregnant mare serum gonadotropin and equine LH also caused a dose-dependent stimulation of estrogen and progesterone production, the half-maximal response values (ED50) being 1.8-4 and 7.5-10 ng/ml, respectively. This is consistent with previous in vivo and in vitro findings, showing the potent FSH activities of these hormones. Thus, the cultured rat granulosa cell system provides a sensitive assay for measuring FSH activities of gonadotropins from various mammalian species.

摘要

在切除垂体并用雌激素预处理的未成熟雌性大鼠的颗粒细胞中,研究了六种哺乳动物来源的促性腺激素刺激雌激素和孕酮产生的能力。颗粒细胞在存在或不存在各种促性腺激素制剂的情况下,于δ4-雄烯二酮(10^(-7) M)存在下培养2天。用人、大鼠、绵羊、猪、马和牛来源的促卵泡素(促卵泡激素,FSH)处理,导致类固醇生成呈剂量依赖性增加,雌激素和孕酮分别从可忽略不计的量增加到约4 - 8 ng/10^5细胞和12 - 30 ng/10^5细胞的最大水平。FSH制剂刺激类固醇生成的半数有效剂量(ED50)值分别为:人:1 - 4 ng/ml;绵羊:2.5 - 30 ng/ml;大鼠:m1.6 - 4.0 ng/ml;猪:7.5 - 20 ng/ml;马:2.5 - 6 ng/ml;牛:大于100 ng/ml。大鼠、绵羊、牛和猪来源的促黄体素(促黄体生成素,LH)、人绒毛膜促性腺激素(hCG)、人FSH的α亚基和人LH的β亚基在刺激类固醇生成方面无效,表明该检测系统对FSH具有特异性。在高浓度(600 ng/ml)下,人FSH的β亚基对类固醇生成有一定程度的刺激作用。此外,孕马血清促性腺激素和马LH也引起雌激素和孕酮产生的剂量依赖性刺激,半数最大反应值(ED50)分别为1.8 - 4 ng/ml和7.5 - 10 ng/ml。这与先前的体内和体外研究结果一致,表明这些激素具有强大的FSH活性。因此,培养的大鼠颗粒细胞系统为测量各种哺乳动物来源促性腺激素的FSH活性提供了一种灵敏检测方法。

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