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本文引用的文献

1
The voltage-gated sodium channel Na1.8 blocker A-803467 inhibits cough in the guinea pig.电压门控钠离子通道 Na1.8 阻断剂 A-803467 抑制豚鼠咳嗽。
Respir Physiol Neurobiol. 2019 Dec;270:103267. doi: 10.1016/j.resp.2019.103267. Epub 2019 Aug 6.
2
Targeting C-fibers for peripheral acting anti-tussive drugs.针对外周作用镇咳药的 C 纤维靶点。
Pulm Pharmacol Ther. 2019 Jun;56:15-19. doi: 10.1016/j.pupt.2019.03.002. Epub 2019 Mar 11.
3
The Role of Voltage-Gated Sodium Channels in Pain Signaling.电压门控钠离子通道在疼痛信号转导中的作用。
Physiol Rev. 2019 Apr 1;99(2):1079-1151. doi: 10.1152/physrev.00052.2017.
4
Lidocaine, a Non-selective Inhibitor of Voltage-Gated Sodium Channels, Blocks Chemically-Induced Cough in Awake Naïve Guinea Pigs.利多卡因,一种电压门控钠离子通道的非选择性抑制剂,可阻断清醒未致敏豚鼠的化学性咳嗽。
Adv Exp Med Biol. 2019;1160:1-9. doi: 10.1007/5584_2018_326.
5
Different role of TTX-sensitive voltage-gated sodium channel (Na 1) subtypes in action potential initiation and conduction in vagal airway nociceptors.不同型 TTX 敏感型电压门控钠离子通道(Na 1)亚型在迷走气道伤害感受器动作电位起始和传导中的作用。
J Physiol. 2018 Apr 15;596(8):1419-1432. doi: 10.1113/JP275698.
6
Melatonin attenuates chronic cough mediated by oxidative stress via transient receptor potential melastatin-2 in guinea pigs exposed to particulate matter 2.5.褪黑素通过瞬时受体电位香草酸亚型2减轻暴露于细颗粒物2.5的豚鼠中由氧化应激介导的慢性咳嗽。
Physiol Res. 2018 May 4;67(2):293-305. doi: 10.33549/physiolres.933654. Epub 2018 Jan 5.
7
Vagotomy decreases the neuronal activities of medulla oblongata and alleviates neurogenic inflammation of airways induced by repeated intra-esophageal instillation of HCl in guinea pigs.迷走神经切断术可降低豚鼠延髓的神经元活动,并减轻因反复经食管灌注盐酸所诱导的气道神经源性炎症。
Physiol Res. 2017 Dec 20;66(6):1021-1028. doi: 10.33549/physiolres.933574. Epub 2017 Sep 22.
8
Effects of a novel sodium channel blocker, GSK2339345, in patients with refractory chronic cough
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Cough and airway disease: The role of ion channels.咳嗽和气道疾病:离子通道的作用。
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强效钠离子电压门控通道阻滞剂缓解过度咳嗽的前景。

The Prospect for Potent Sodium Voltage-Gated Channel Blockers to Relieve an Excessive Cough.

机构信息

Department of Pathophysiology, Jessenius Faculty of Medicine, Comenius University, Martin, Slovakia.

出版信息

Physiol Res. 2020 Mar 27;69(Suppl 1):S7-S18. doi: 10.33549/physiolres.934395.

DOI:10.33549/physiolres.934395
PMID:32228007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8604057/
Abstract

An excessive, irritable, productive or non-productive coughing associated with airway inflammation belongs to pathological cough. Increased activation of airway vagal nociceptors in pathological conditions results from dysregulation of the neural pathway that controls cough. A variety of mediators associated with airway inflammation overstimulate these vagal airway fibers including C-fibers leading to hypersensitivity and hyperreactivity. Because current antitussives have limited efficacy and unwanted side effects there is a continual demand for the development of a novel more effective antitussives for a new efficacious and safe cough treatment. Therefore, inhibiting the activity of these vagal C-fibers represents a rational approach to the development of effective antitussive drugs. This may be achieved by blocking inflammatory mediator receptors or by blocking the generator potential associated with the specific ion channels. Because voltage-gated sodium channels (NaVs) are absolutely required for action potentials initiation and conduction irrespective of the stimulus, NaVs become a promising neural target. There is evidence that NaV1.7, 1.8 and 1.9 subtypes are predominantly expressed in airway cough-triggering nerves. The advantage of blocking these NaVs is suppressing C-fiber irrespective to stimuli, but the disadvantage is that by suppressing the nerves is may also block beneficial sensations and neuronal reflex behavior. The concept is that new antitussive drugs would have the benefit of targeting peripheral airway nociceptors without inhibiting the protective cough reflex.

摘要

与气道炎症相关的过度、烦躁、产生或不产生分泌物的咳嗽属于病理性咳嗽。在病理条件下,气道迷走神经伤害感受器的过度激活是由于控制咳嗽的神经通路失调所致。与气道炎症相关的各种介质过度刺激这些迷走气道纤维,包括 C 纤维,导致超敏性和高反应性。由于目前的镇咳药疗效有限且有不良副作用,因此不断需要开发新的、更有效的镇咳药来进行有效的、安全的咳嗽治疗。因此,抑制这些迷走 C 纤维的活性代表了开发有效镇咳药物的合理方法。这可以通过阻断炎症介质受体或阻断与特定离子通道相关的发生器潜能来实现。因为电压门控钠离子通道(NaVs)是无论刺激如何都绝对需要引发和传导动作电位的,因此 NaVs 成为了一个有前途的神经靶点。有证据表明,NaV1.7、1.8 和 1.9 亚型主要在气道咳嗽触发神经中表达。阻断这些 NaVs 的优点是抑制 C 纤维而不受刺激影响,但缺点是通过抑制神经也可能阻断有益的感觉和神经元反射行为。其理念是,新型镇咳药将具有靶向外周气道伤害感受器的优势,而不会抑制保护性咳嗽反射。