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促黄体生成素释放介质对垂体促性腺细胞的脱敏作用。

Desensitization of pituitary gonadotropes by mediators of LH release.

作者信息

Chang J P, Graeter J S, Catt K J

机构信息

Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, Bethesda, MD 20892.

出版信息

Biochem Biophys Res Commun. 1988 Jun 30;153(3):919-24. doi: 10.1016/s0006-291x(88)81315-9.

Abstract

Desensitization of pituitary gonadotropes by exposure to 10 nM gonadotropin-releasing hormone (GnRH) for 6 h severely impaired the luteinizing hormone (LH) response to a second 3-h treatment with GnRH, and reduced the secretory responses to 50 microM arachidonic acid (AA), 100 nM tetradecanoyl phorbol-13-acetate (TPA), and AA + TPA. Pretreatment with AA blocked subsequent responses to AA but not to other secretagogues. Pretreatment with TPA attenuated the LH response to TPA, but not to GnRH, AA, and AA + TPA. After exposure to AA + TPA, all subsequent responses were abolished. Each of the secretagogues reduced GnRH receptor binding, but only GnRH-induced receptor loss and desensitization were reversed by simultaneous incubation with a GnRH antagonist. Similar results were obtained when 16-h pretreatment periods were used, or when the data were normalized for the concomitant reduction of cellular LH content. These findings indicate that GnRH-receptor loss and depletion of LH content are not the sole causes of GnRH-induced desensitization. Receptor uncoupling and impairment of AA- and protein kinase C-dependent pathways may also be involved in this process.

摘要

垂体促性腺细胞经10 nM促性腺激素释放激素(GnRH)处理6小时后发生脱敏,严重损害了促黄体生成素(LH)对第二次3小时GnRH处理的反应,并降低了对50 μM花生四烯酸(AA)、100 nM十四酰佛波醇-13-乙酸酯(TPA)以及AA + TPA的分泌反应。用AA预处理可阻断随后对AA的反应,但不影响对其他促分泌剂的反应。用TPA预处理可减弱LH对TPA的反应,但不影响对GnRH、AA以及AA + TPA的反应。暴露于AA + TPA后,所有随后的反应均被消除。每种促分泌剂均降低GnRH受体结合,但只有与GnRH拮抗剂同时孵育才能逆转GnRH诱导的受体丢失和脱敏。当采用16小时预处理期,或对伴随的细胞LH含量降低进行数据归一化处理时,也获得了类似结果。这些发现表明,GnRH受体丢失和LH含量减少并非GnRH诱导脱敏的唯一原因。受体解偶联以及AA和蛋白激酶C依赖性途径的损害可能也参与了这一过程。

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