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在原代培养中,孕酮对大鼠垂体前叶促肾上腺皮质激素抑制β-内啡肽释放的抗糖皮质激素作用的证明。

Demonstration of an antiglucocorticoid action of progesterone on the corticosterone inhibition of beta-endorphin release by rat anterior pituitary in primary culture.

作者信息

Abou Samra A B, Loras B, Pugeat M, Tourniaire J, Bertrand J

出版信息

Endocrinology. 1984 Oct;115(4):1471-5. doi: 10.1210/endo-115-4-1471.

Abstract

The effects of progesterone or 17 alpha-hydroxyprogesterone on corticosterone regulation of beta-endorphin (beta-end) release have been studied in vitro using primary culture of rat anterior pituitaries. Incubation of pituitary cells with ovine corticotropin-releasing factor (CRF) for 2 h resulted in a dose-dependent increase in beta-end release. Maximal stimulation was obtained with 200 ng/ml CRF. Preincubation for 2 h with corticosterone resulted in a dose-dependent inhibition of CRF-induced beta-end release. When the cultures were preincubated for 2 h with 200 ng/ml corticosterone and increasing concentrations (1, 10, 100, 1,000, and 10,000 ng/ml) of progesterone, a significant decrease in the corticosterone feedback action was observed with 100 ng/ml progesterone. Complete inhibition of the action of 200 ng/ml corticosterone was achieved with 10,000 ng/ml progesterone. Moreover, when the cultures were preincubated with increasing concentrations of corticosterone in the presence of 100 ng/ml progesterone, the ED50 of corticosterone increased significantly from 212 +/- 36 to 940 +/- 42 ng/ml (mean +/- SEM; P less than 0.01). Under the same conditions, 17 alpha-hydroxyprogesterone had no effect. These data demonstrate that progesterone antagonizes the corticosterone feedback inhibition of beta-end release by rat anterior pituitary.

摘要

利用大鼠垂体前叶原代培养物在体外研究了孕酮或17α-羟孕酮对促肾上腺皮质激素释放因子(CRF)调节β-内啡肽(β-end)释放的影响。垂体细胞与羊促肾上腺皮质激素释放因子(CRF)孵育2小时导致β-end释放呈剂量依赖性增加。200 ng/ml CRF可获得最大刺激。与皮质酮预孵育2小时导致CRF诱导的β-end释放呈剂量依赖性抑制。当培养物用200 ng/ml皮质酮和递增浓度(1、10、100、1000和10000 ng/ml)的孕酮预孵育2小时时,观察到100 ng/ml孕酮可使皮质酮的反馈作用显著降低。10000 ng/ml孕酮可完全抑制200 ng/ml皮质酮的作用。此外,当培养物在100 ng/ml孕酮存在下用递增浓度的皮质酮预孵育时,皮质酮的半数有效剂量(ED50)从212±36显著增加至940±42 ng/ml(平均值±标准误;P<0.01)。在相同条件下,17α-羟孕酮无作用。这些数据表明,孕酮可拮抗大鼠垂体前叶皮质酮对β-end释放的反馈抑制作用。

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