Suppr超能文献

血管紧张素受体与去甲肾上腺素神经调节:功能偶联的影响

Angiotensin receptors and norepinephrine neuromodulation: implications of functional coupling.

作者信息

Gelband C H, Sumners C, Lu D, Raizada M K

机构信息

Department of Physiology, College of Medicine, University of Florida, Gainesville 32610, USA.

出版信息

Regul Pept. 1998 Feb 27;73(3):141-7. doi: 10.1016/s0167-0115(97)11050-3.

Abstract

The objective of this review is to examine the role of neuronal angiotensin II (Ang II) receptors in vitro. Two types of G protein-coupled Ang II receptors have been identified in cardiovascularly relevant areas of the brain: the AT1 and the AT2. We have utilized neurons in culture to study the signaling mechanisms of AT1 and AT2 receptors. Neuronal AT1 receptors are involved in norepinephrine (NE) neuromodulation. NE neuromodulation can be either evoked or enhanced. Evoked NE neuromodulation involves AT1 receptor-mediated, losartan-dependent, rapid NE release, inhibition of K+ channels and stimulation of Ca2+ channels. AT1 receptor-mediated enhanced NE neuromodulation involves the Ras-Raf-MAP kinase cascade and ultimately leads to an increase in NE transporter, tyrosine hydroxylase and dopamine beta-hydroxylase mRNA transcription. Neuronal AT2 receptors signal via a Gi protein and are coupled to activation of PP2A and PLA2 and stimulation of K+ channels. Finally, putative cross-talk pathways between AT1 and AT2 receptors will be discussed.

摘要

本综述的目的是研究神经元血管紧张素II(Ang II)受体在体外的作用。在大脑与心血管相关的区域已鉴定出两种类型的G蛋白偶联Ang II受体:AT1和AT2。我们利用培养的神经元来研究AT1和AT2受体的信号传导机制。神经元AT1受体参与去甲肾上腺素(NE)的神经调节。NE神经调节可以被诱发或增强。诱发的NE神经调节涉及AT1受体介导的、氯沙坦依赖性的快速NE释放、钾通道抑制和钙通道刺激。AT1受体介导的增强NE神经调节涉及Ras-Raf-MAP激酶级联反应,并最终导致NE转运体、酪氨酸羟化酶和多巴胺β-羟化酶mRNA转录增加。神经元AT2受体通过Gi蛋白发出信号,并与PP2A和PLA2的激活以及钾通道的刺激偶联。最后,将讨论AT1和AT2受体之间可能的相互作用途径。

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