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GT1促性腺激素释放激素(GnRH)神经元细胞系的多巴胺能调节:通过与腺苷酸环化酶正向偶联的D1受体刺激GnRH释放。

Dopaminergic regulation of the GT1 gonadotropin-releasing hormone (GnRH) neuronal cell lines: stimulation of GnRH release via D1-receptors positively coupled to adenylate cyclase.

作者信息

Martínez de la Escalera G, Gallo F, Choi A L, Weiner R I

机构信息

Department of Obstetrics, Gynecology and Reproductive Sciences, University of California School of Medicine, San Francisco 94143.

出版信息

Endocrinology. 1992 Dec;131(6):2965-71. doi: 10.1210/endo.131.6.1280208.

Abstract

The release of GnRH evoked by dopamine (DA) was studied in the GT1 GnRH neuronal cell lines. Superfusion of GT1-1 cells with DA or the D1-dopaminergic agonist SKF 38393, but not with the D2-dopaminergic agonist bromocriptine, increased 2-fold the amplitude of the spontaneous GnRH pulses. Treatment with DA for 30 min also stimulated GnRH release from static cultures of GT1-7 cells. This effect was mimicked by the selective D1-dopaminergic agonist SKF 38393 and blocked by the D1-dopaminergic antagonist SCH 23390. However, the D2-dopaminergic agonist bromocriptine had no effect, and the stimulation of GnRH release by DA was not blocked by the D2-dopaminergic antagonist spiroperidol. In parallel to the stimulation of GnRH release, DA also rapidly increased (first observed at 120 sec) in a dose-dependent fashion, the intracellular concentration of cAMP in isobutylmethylxanthine-pretreated GT1-7 cells. The pharmacological profile of the increase in cAMP was identical to that for GnRH release. The cAMP responses to DA and norepinephrine were lost after long term treatment with SKF 38393, i.e. heterologous desensitization. GT1 cells also express the mRNA for the dopamine- and cAMP-regulated phospho-protein (mol wt, 32,000; DARPP-32) only seen in cells expressing DA D1-receptors. These results demonstrate a direct stimulatory effect of DA on GnRH release via DA D1-receptors positively coupled to adenylate cyclase in GnRH neuronal cell lines.

摘要

在GT1促性腺激素释放激素(GnRH)神经元细胞系中研究了多巴胺(DA)诱发的GnRH释放情况。用DA或D1 - 多巴胺能激动剂SKF 38393对GT1 - 1细胞进行灌流,但不用D2 - 多巴胺能激动剂溴隐亭灌流,可使自发性GnRH脉冲的幅度增加2倍。用DA处理30分钟也能刺激GT1 - 7细胞静态培养物释放GnRH。这种效应可被选择性D1 - 多巴胺能激动剂SKF 38393模拟,并被D1 - 多巴胺能拮抗剂SCH 23390阻断。然而,D2 - 多巴胺能激动剂溴隐亭没有作用,并且DA对GnRH释放的刺激作用不会被D2 - 多巴胺能拮抗剂螺哌啶阻断。与GnRH释放的刺激作用同时,DA还能以剂量依赖的方式迅速增加(在120秒时首次观察到)异丁基甲基黄嘌呤预处理的GT1 - 7细胞内的环磷酸腺苷(cAMP)浓度。cAMP增加的药理学特征与GnRH释放的特征相同。在用SKF 38393长期处理后,对DA和去甲肾上腺素的cAMP反应消失,即发生了异源脱敏。GT1细胞还表达多巴胺和cAMP调节的磷蛋白(分子量32,000;DARPP - 32)的信使核糖核酸(mRNA),这种蛋白仅在表达DA D1受体的细胞中可见。这些结果表明,在GnRH神经元细胞系中,DA通过与腺苷酸环化酶正性偶联的DA D1受体对GnRH释放具有直接的刺激作用。

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