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体外促性腺激素对催乳素介导的孕酮分泌的调节作用

Gonadotrophic regulation of prolactin mediated progesterone secretion in vitro.

作者信息

Alexander J S, Crisp T M

出版信息

Acta Endocrinol (Copenh). 1985 Oct;110(2):251-6. doi: 10.1530/acta.0.1100251.

Abstract

The effects of preincubating rat granulosa cells with FSH, LH, and Prl on subsequent Prl mediated progesterone secretion were investigated. Granulosa cells were isolated from ovarian follicles 50 h after injection of 5 IU PMSG and were then plated on poly-L-lysine coated coverslips in serum supplemented medium. Cells were preincubated for 24 h in the absence of hormones (control) or with the addition of either 0.25, 2.5, 25 ng/ml rat FSH or rat LH, or 1 microgram/ml rat Prl. Following the preincubation period, cells were maintained for an additional 6 or 8 days in the presence or absence of 1 microgram/ml Prl. When cells were preincubated with FSH or LH, only the two higher concentrations (2.5 and 25 ng/ml) stimulated significantly more progesterone secretion than control cultures during the 24 h preincubation period. For each series of preincubations, cells cultured for 6 or 8 days in the presence of Prl secreted significantly more progesterone at each day of culture than cells cultured without Prl. Cells preincubated and cultured with Prl secreted only 3-7-fold more progesterone than cells preincubated in control medium and then cultured with Prl. Preincubation with FSH or LH promoted a 20-45-fold increase in Prl mediated progesterone secretion compared to control preincubation cultures that also subsequently were cultured with Prl. The magnitude of Prl mediated progesterone secretion observed through 6 days of culturing was dose dependent on the preincubation concentration of FSH or LH.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了用促卵泡激素(FSH)、促黄体生成素(LH)和催乳素(Prl)预孵育大鼠颗粒细胞对随后Prl介导的孕酮分泌的影响。在注射5国际单位孕马血清促性腺激素(PMSG)50小时后,从卵巢卵泡中分离出颗粒细胞,然后将其接种在涂有聚-L-赖氨酸的盖玻片上,置于补充血清的培养基中。细胞在无激素(对照)的情况下预孵育24小时,或添加0.25、2.5、25纳克/毫升大鼠FSH或大鼠LH,或1微克/毫升大鼠Prl。预孵育期后,细胞在有或无1微克/毫升Prl的情况下再维持培养6或8天。当细胞用FSH或LH预孵育时,在24小时预孵育期内,只有两个较高浓度(2.5和25纳克/毫升)刺激孕酮分泌显著多于对照培养物。对于每一系列预孵育,在有Prl存在的情况下培养6或8天的细胞,在培养的每一天分泌的孕酮都显著多于无Prl培养的细胞。用Prl预孵育和培养的细胞分泌的孕酮仅比在对照培养基中预孵育然后用Prl培养的细胞多3 - 7倍。与同样随后用Prl培养的对照预孵育培养物相比,用FSH或LH预孵育可促进Prl介导的孕酮分泌增加20 - 45倍。通过6天培养观察到的Prl介导的孕酮分泌量在剂量上取决于FSH或LH的预孵育浓度。(摘要截短至250字)

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