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血管紧张素II在口渴、钠食欲、认知和记忆方面的神经元作用。

The neuronal role of angiotensin II in thirst, sodium appetite, cognition and memory.

作者信息

Mosimann R, Imboden H, Felix D

机构信息

Division of Neurobiology, University of Berne, Switzerland.

出版信息

Biol Rev Camb Philos Soc. 1996 Nov;71(4):545-59. doi: 10.1111/j.1469-185x.1996.tb01284.x.

Abstract

Within the past two decades, a great deal has been learnt about the renin-angiotensin system in the brain. The renin-angiotensin system is one of the best-studied enzyme-neuropeptide systems in the brain. The diversity of localization of this peptide throughout the brain has implied a variety of potential functions. Besides its classical role in the regulation of blood pressure and body-fluid homeostasis, it has more subtle functions involving complex mechanisms such as learning and memory. The profound effects on behaviour produced by angiotensin are of broad interest to neuroscientists. The mechanisms of action differ depending on whether angiotensin is locally synthesized and whether regulation is governed by neural or metabolic inputs impinging on the neurones. Its central action is mediated through peptidergic receptors present on neurones. The description of the receptor subtypes AT1 and AT2 for angiotensin II and the development of non-peptidic specific angiotensin receptor subtype antagonists have opened a new area in this field of research. The AT1 site, which preferentially binds to angiotensin II and angiotensin III, appears to mediate the classical angiotensin functions concerned with maintenance of blood pressure and body-fluid control. In addition, most of the behavioural effects described so far are linked with AT1, although so-called psychotropic effects are presumed to be mediated by receptor systems other than the known specific angiotensin receptors. In fact, evidence for the existence of such receptors with high-affinity binding has been reported. The central action of angiotensin II mediated by AT2 is as yet unclear. Most reports concerning this receptor subtype suggest a role in differentiation and development, since the number of binding sites is higher in fetal and young rats than in adults. Furthermore, the neuronal effect of angiotensin II in the inferior olivary nucleus which is blocked specifically by AT2 antagonists suggests an involvement in motor control. Over the next few years we should find answers to many of the questions currently unanswered about angiotensin function and, given the rapid progress in research on this neuropeptide, it may serve as a model for the action of peptides on neuronal function in general.

摘要

在过去二十年中,人们对大脑中的肾素-血管紧张素系统已有很多了解。肾素-血管紧张素系统是大脑中研究最为深入的酶-神经肽系统之一。这种肽在大脑中的定位多样性暗示了其多种潜在功能。除了在调节血压和体液平衡方面的经典作用外,它还具有涉及学习和记忆等复杂机制的更微妙功能。血管紧张素对行为产生的深远影响引起了神经科学家的广泛关注。其作用机制因血管紧张素是局部合成的,以及调节是否受影响神经元的神经或代谢输入控制而有所不同。它的中枢作用是通过神经元上存在的肽能受体介导的。血管紧张素 II 的受体亚型 AT1 和 AT2 的描述以及非肽类特异性血管紧张素受体亚型拮抗剂的开发,为该研究领域开辟了一个新方向。AT1 位点优先与血管紧张素 II 和血管紧张素 III 结合,似乎介导了与维持血压和体液控制相关的经典血管紧张素功能。此外,迄今为止描述的大多数行为效应都与 AT1 相关,尽管所谓的精神otropic 效应被认为是由已知的特异性血管紧张素受体以外的受体系统介导的。事实上,已经报道了存在具有高亲和力结合的此类受体的证据。由 AT2 介导的血管紧张素 II 的中枢作用尚不清楚。关于该受体亚型的大多数报告表明其在分化和发育中起作用,因为胎儿和幼鼠中的结合位点数量高于成年鼠。此外,血管紧张素 II 在延髓下橄榄核中的神经元效应被 AT2 拮抗剂特异性阻断,表明其参与运动控制。在接下来的几年里,我们应该能够找到许多目前关于血管紧张素功能尚未解答的问题的答案,而且鉴于对这种神经肽的研究进展迅速,它可能总体上作为肽对神经元功能作用的一个模型。

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