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离子型和代谢型受体介导的气道感觉神经激活。

Ionotropic and metabotropic receptor mediated airway sensory nerve activation.

作者信息

Lee Min-Goo, Kollarik Marian, Chuaychoo Benjamas, Undem Bradley J

机构信息

Johns Hopkins Asthma and Allergy Center, 5501-Hopkins Bayview Circle, Baltimore, MD 21224, USA.

出版信息

Pulm Pharmacol Ther. 2004;17(6):355-60. doi: 10.1016/j.pupt.2004.09.025.

Abstract

There are several receptors capable of inducing activating generator potentials in cough-associated afferent terminals in the airways. The chemical receptors leading to generator potentials can be subclassified into ionotropic and metabotropic types. An ionotropic receptor has an agonist-binding domain, and also serves directly as an ion channel that is opened upon binding of the agonist. Examples of ionotropic receptors found in airway sensory nerve terminals include receptors for serotonin (5-HT3 receptors), ATP (P2X receptors), acetylcholine (nicotinic receptors), receptors for capsaicin and related vanilloids (TRPV1 receptors), and acid receptors (acid sensing ion channels). Afferent nerve terminals can also be depolarized via activation of metabotropic or G-protein coupled receptors (GPCRs). Among the GPCRs that can lead to activation of airway afferent fibers include bradykinin B2 and adenosine A1 receptors. The signaling events leading to GPCR-mediated membrane depolarization are more complex than that seen with ionotropic receptors. The GPCR-mediated effects are thought to occur through classical second messenger systems such as activation of phospholipase C. This may lead to membrane depolarization through interaction with specific ionotropic receptors (such as TRPV1) and/or various types of calcium activated channels.

摘要

有几种受体能够在气道中与咳嗽相关的传入神经末梢诱导激活发生器电位。导致发生器电位的化学感受器可分为离子型和代谢型。离子型受体有一个激动剂结合域,并且直接作为一个在激动剂结合时打开的离子通道。在气道感觉神经末梢发现的离子型受体的例子包括5-羟色胺受体(5-HT3受体)、ATP受体(P2X受体)、乙酰胆碱受体(烟碱受体)、辣椒素及相关香草酸受体(TRPV1受体)和酸受体(酸敏感离子通道)。传入神经末梢也可通过代谢型或G蛋白偶联受体(GPCR)的激活而发生去极化。可导致气道传入纤维激活的GPCR包括缓激肽B2受体和腺苷A1受体。导致GPCR介导的膜去极化的信号事件比离子型受体所见的更为复杂。GPCR介导的效应被认为是通过经典的第二信使系统发生的,如磷脂酶C的激活。这可能通过与特定的离子型受体(如TRPV1)和/或各种类型的钙激活通道相互作用而导致膜去极化。

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