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内源性哇巴因的生理效应:细胞内钙库的调控与细胞反应性

Physiological effects of endogenous ouabain: control of intracellular Ca2+ stores and cell responsiveness.

作者信息

Blaustein M P

机构信息

Department of Physiology, University of Maryland School of Medicine, Baltimore 21201.

出版信息

Am J Physiol. 1993 Jun;264(6 Pt 1):C1367-87. doi: 10.1152/ajpcell.1993.264.6.C1367.

Abstract

Ouabain is a well-known compound but a newly discovered adrenal cortical hormone that plays a role in cell Na+ regulation and in whole body salt and water balance. Ouabain may also be a paracrine hormone and may be secreted by some central nervous system neurons as well as by other types of cells. This article focuses on the cellular mechanisms that underlie the physiological (and pathophysiological) effects of ouabain. Ouabain directly inhibits the plasmalemmal Na+ pump in a variety of cell types. Low ouabain concentrations cause, in the steady state, a modest rise in the cytosolic Na+ concentration but only a minimal decline in membrane potential. All Na+ gradient-dependent processes may thereby be affected, albeit to only a small extent. Most important, however, is the secondary redistribution of Ca2+, mediated by Na(+)-Ca2+ exchange, that should slightly increase the cytosolic free Ca2+ concentration ([Ca2+]cyt). As a result of Ca2+ sequestration in intracellular stores [the endoplasmic and/or sarcoplasmic reticulum (ER/SR)], however, a new steady state is achieved with a slightly increased [Ca2+]cyt but a substantially augmented Ca2+ store; thus the ER/SR effectively acts as a Ca2+ amplifier. This extra stored Ca2+ is then available for mobilization whenever the cells are activated. Cytosolic Ca2+ is a key signaling mechanism in virtually all cells: it controls numerous physiological processes such as contraction, secretion, and excitability. Thus ouabain may modulate cell responsiveness via its influence on ER/SR Ca2+ stores. With these principles in mind, we examine evidence that endogenous ouabain may play a role in numerous physiological and pathophysiological processes associated with altered fluid and electrolyte metabolism and deviations from the normal blood pressure-blood volume relationship. We discuss the possible participation of ouabain in the regulation of vascular tone and then consider the putative role of ouabain in several forms of hypertension, congestive heart failure, thyroid and adrenocortical dysfunction, and diabetes mellitus, as well as in the adaptation to high altitude.

摘要

哇巴因是一种广为人知的化合物,但却是一种新发现的肾上腺皮质激素,它在细胞钠离子调节以及全身盐和水平衡中发挥作用。哇巴因也可能是一种旁分泌激素,可能由一些中枢神经系统神经元以及其他类型的细胞分泌。本文重点关注哇巴因生理(和病理生理)效应背后的细胞机制。哇巴因能直接抑制多种细胞类型的质膜钠泵。在稳态下,低浓度的哇巴因会使胞质钠离子浓度适度升高,但膜电位仅轻微下降。所有依赖钠离子梯度的过程可能因此受到影响,尽管程度较小。然而,最重要的是由钠钙交换介导的钙离子二次重分布,这会使胞质游离钙离子浓度([Ca2+]cyt)略有增加。然而,由于钙离子被隔离在细胞内储存库[内质网和/或肌浆网(ER/SR)]中,会达到一个新的稳态,此时[Ca2+]cyt略有增加,但钙离子储存库大幅增大;因此,ER/SR实际上起到了钙离子放大器的作用。每当细胞被激活时,这些额外储存的钙离子就可用于动员。胞质钙离子实际上是所有细胞中的关键信号机制:它控制着许多生理过程,如收缩、分泌和兴奋性。因此,哇巴因可能通过影响ER/SR钙离子储存库来调节细胞反应性。基于这些原理,我们研究了内源性哇巴因可能在与液体和电解质代谢改变以及偏离正常血压-血容量关系相关的众多生理和病理生理过程中发挥作用的证据。我们讨论了哇巴因在血管张力调节中的可能参与情况,然后考虑了哇巴因在几种高血压、充血性心力衰竭、甲状腺和肾上腺皮质功能障碍、糖尿病以及高原适应中的假定作用。

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