Suppr超能文献

雌激素对中枢神经系统(CNS)中钾通道G蛋白偶联受体激活的快速作用。

Rapid effects of estrogen on G protein-coupled receptor activation of potassium channels in the central nervous system (CNS).

作者信息

Kelly Martin J, Qiu Jian, Wagner Edward J, Rønnekleiv Oline K

机构信息

Department of Physiology and Pharmacology, L334 Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97201, USA.

出版信息

J Steroid Biochem Mol Biol. 2002 Dec;83(1-5):187-93. doi: 10.1016/s0960-0760(02)00249-2.

Abstract

Estrogen rapidly alters the excitability of hypothalamic neurons that are involved in regulating numerous homeostatic functions including reproduction, stress responses, feeding and motivated behaviors. Some of the neurons include neurosecretory neurons such as gonadotropin-releasing hormone (GnRH) and dopamine neurons, and local circuitry neurons such as proopiomelanocortin (POMC) and gamma-aminobutyric acid (GABA) neurons. We have elucidated several non-genomic pathways through which the steroid alters synaptic responses in these hypothalamic neurons. We have examined the modulation by estrogen of the coupling of various receptor systems to inwardly-rectifying and small-conductance, Ca(2+)-activated K(+) (SK) channels using intracellular sharp-electrode and whole-cell recording techniques in hypothalamic slices from ovariectomized female guinea pigs. Estrogen rapidly uncouples mu-opioid receptors from G protein-gated inwardly-rectifying K(+) (GIRK) channels in POMC neurons and GABA(B) receptors from GIRK channels in dopamine neurons as manifested by a reduction in the potency of mu-opioid and GABA(B) receptor agonists to hyperpolarize their respective cells. This effect is blocked by inhibitors of protein kinase A (PKA) and protein kinase C (PKC). In addition, after 24h following steroid administration in vivo, the GABA(B)/GIRK channel uncoupling observed in GABAergic neurons of the preoptic area is associated with reduced agonist efficacy. Conversely, estrogen enhances the efficacy of alpha(1)-adrenergic receptor agonists to inhibit apamin-sensitive SK currents in these preoptic GABAergic neurons, and does so in both a rapid and sustained fashion. Finally, we observed a direct, steroid-induced hyperpolarization of GnRH neurons. These findings indicate a richly complex yet coordinated steroid modulation of K(+) channel activity in hypothalamic (POMC, dopamine, GABA, GnRH) neurons that are involved in regulating numerous homeostatic functions.

摘要

雌激素能迅速改变下丘脑神经元的兴奋性,这些神经元参与调节多种稳态功能,包括生殖、应激反应、进食和动机行为。其中一些神经元包括神经分泌神经元,如促性腺激素释放激素(GnRH)和多巴胺能神经元,以及局部回路神经元,如阿黑皮素原(POMC)和γ-氨基丁酸(GABA)能神经元。我们已经阐明了几种非基因组途径,通过这些途径,类固醇可改变这些下丘脑神经元的突触反应。我们使用细胞内尖锐电极和全细胞记录技术,在去卵巢雌性豚鼠的下丘脑切片中,研究了雌激素对各种受体系统与内向整流和小电导、Ca(2+)激活的K(+)(SK)通道耦合的调节作用。雌激素能迅速使POMC神经元中的μ-阿片受体与G蛋白门控内向整流K(+)(GIRK)通道解偶联,使多巴胺能神经元中的GABA(B)受体与GIRK通道解偶联,表现为μ-阿片和GABA(B)受体激动剂使各自细胞超极化的效力降低。这种效应被蛋白激酶A(PKA)和蛋白激酶C(PKC)的抑制剂所阻断。此外,在体内给予类固醇24小时后,视前区GABA能神经元中观察到的GABA(B)/GIRK通道解偶联与激动剂效力降低有关。相反,雌激素增强了α(1)-肾上腺素能受体激动剂抑制这些视前区GABA能神经元中蜂毒明肽敏感的SK电流的效力,且这种增强作用是快速且持续的。最后,我们观察到GnRH神经元出现直接的、类固醇诱导的超极化。这些发现表明,下丘脑(POMC、多巴胺、GABA、GnRH)神经元中K(+)通道活性受到丰富复杂但协调的类固醇调节作用,这些神经元参与调节多种稳态功能。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验