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首页> 外文期刊>Molecular Aspects of Medicine: An Interdisciplinary Review Journal >Oxygen-sensing by arterial chemoreceptors: Mechanisms and medical translation
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Oxygen-sensing by arterial chemoreceptors: Mechanisms and medical translation

机译:动脉化学感受器的氧气感应:机制和医学翻译

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摘要

Acute O2 sensing is necessary for the activation of cardiorespiratory reflexes (hyperventilation and sympathetic activation), which permit the survival of individuals under hypoxic environments (e.g. high altitude) or medical conditions presenting with reduced capacity for gas exchange between the lung alveoli and the blood. Changes in blood O2 tension are detected by the arterial chemoreceptors, in particular the carotid body (CB), which act in concert with the adrenal medulla (AM) to facilitate rapid adaptations to hypoxia. The field of arterial chemoreception has undergone a considerable expansion in recent years, with many of the fundamental observations made at the molecular and cellular levels serving to improve our understanding of the pathogenesis of numerous medical disorders, and even to propose advances in the treatment strategies. In this review, after a short historical preface, we describe the current model of chemosensory transduction based on the modulation of membrane K+ channels by O2 in specialized chemoreceptor cells. Recent progress in elucidating the molecular mechanisms underlying the modulation of ion channels by O2 tension, which involves mitochondrial complex I, is also discussed. The discovery in the last few years of a specific population of neural crest-derived stem cells in the CB explains the reversible growth of this organ, an intriguing and unusual property of this type of neuronal tissue that contributes to acclimatization under chronic hypoxia. The essential homeostatic role of the CB-AM axis is clearly evident in newly generated mouse models that reach adulthood, albeit with CB and AM atrophy. These animals exhibit a marked intolerance to even mild hypoxia. CB inhibition or over-activation can have important medical consequences. Respiratory depression by general anesthetics or by opioid use is a common clinical condition that frequently causes death in susceptible individuals. An exaggerated sympathetic outflow due to over-activation of the CB-AM axis may contribute to the pathogenesis of several highly prevalent medical conditions, such as chronic heart failure, obstructive sleep apnea, obesity, metabolic syndrome, and diabetes. A detailed understanding of the molecular mechanisms underlying acute O2 sensing may help in the design of more efficient therapeutic approaches to combat these disorders. 2015 Elsevier Ltd. All rights reserved.
机译:急性O2感测是激活心肺反射(过度通气和交感神经激活)的激活,这允许在缺氧环境下存活(例如高海拔)或在肺部肺泡和血液之间的气体交换能力降低的情况下呈现的医疗条件。血液O2张力的变化由动脉化学感受器检测,特别是颈体(CB),其与肾上腺髓质(AM)一起行动,以促进快速适应缺氧。近年来,动脉化学素的领域经历了相当大的扩张,许多基本观测结果在分子和细胞水平上进行了用于改善我们对大量医学障碍的发病机制的理解,甚至提出治疗策略的进步。在本综述中,经过短暂的历史序言,我们描述了基于膜K +通道的调节在专用化学聚细胞中的膜K +通道的当前模型。还讨论了通过O2张力调节离子通道的分子机制的最新进展,这涉及线粒体复合物I的离子通道的调节。 CB中最近几年的发现在特定的神经嵴衍生的干细胞中的特定群体解释了这种器官的可逆生长,这种类型的神经元组织的有趣和不寻常的性质,这有助于在慢性缺氧下的适应性化。 CB-AM轴的基本稳态作用在新生的小鼠模型中显而易见的,该模型达到成年,虽然是Cb和萎缩。这些动物表现出显着的不耐受性甚至轻度缺氧。 Cb抑制或过度激活可以具有重要的医疗后果。通用麻醉剂或阿片类药物的呼吸抑制是一种常见的临床状况,经常导致易感个体死亡。由于CB-AM轴的过度激活而夸大的交感神经流出可能有助于若干高度普遍的医疗病症的发病机制,例如慢性心力衰竭,阻塞性睡眠呼吸暂停,肥胖,代谢综合征和糖尿病。详细了解急性O2感测的分子机制可以有助于设计更有效的治疗方法来解决这些疾病。 2015 Elsevier Ltd.保留所有权利。

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