López-López José Ramón, Pérez-García M Teresa
Departamento de Bioquímica y Biología Molecular y Fisiología, Facultad de Medicina e Instituto de Biología y Genética Molecular, Universidad de Valladolid y Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Respir Physiol Neurobiol. 2007 Jul 1;157(1):65-74. doi: 10.1016/j.resp.2007.01.022. Epub 2007 Mar 4.
Hypoxic inhibition of K(+) channels has been documented in many native chemoreceptor cells, and is crucial to initiate reflexes directed to improve tissue O(2) supply. In the carotid body (CB) chemoreceptors, there is a general consensus regarding the facts that a decrease in P(O2) leads to membrane depolarization, increase of Ca(2+) entry trough voltage-dependent Ca(2+) channels and Ca(2+)-dependent release of neurotransmitters. Central to this pathway is the modulation by hypoxia of K(+) channels that triggers depolarization. However, the details of this process are still controversial, and even the molecular nature of these oxygen-sensitive K(+) (K(O2)) channels in the CB is hotly debated. Clearly there are inter-species differences, and even in the same preparation more that one K(O2) may be present. Here we recapitulate our present knowledge of the role of voltage dependent K(+) channels as K(O2) in the CB from different species, and their functional contribution to cell excitability in response to acute and chronic exposure to hypoxia.
缺氧对钾离子通道的抑制作用已在许多天然化学感受器细胞中得到证实,并且对于启动旨在改善组织氧供应的反射至关重要。在颈动脉体(CB)化学感受器中,关于以下事实存在普遍共识:氧分压(P(O2))降低会导致膜去极化、通过电压依赖性钙通道的钙内流增加以及钙依赖性神经递质释放。该途径的核心是缺氧对钾离子通道的调节,从而引发去极化。然而,这一过程的细节仍存在争议,甚至CB中这些氧敏感钾离子(K(O2))通道的分子性质也备受热议。显然存在种间差异,甚至在同一实验制剂中可能存在不止一种K(O2)通道。在此,我们概述了目前关于电压依赖性钾离子通道作为不同物种CB中的K(O2)通道的作用,以及它们在急性和慢性缺氧暴露下对细胞兴奋性的功能贡献的认识。