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Isoflurane depolarizes bronchopulmonary C neurons by inhibiting transient A-type and delayed rectifier potassium channels.异氟醚通过抑制瞬时 A 型和延迟整流钾通道使支气管肺 C 神经元去极化。
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2
Activation of opioid μ-receptors, but not δ- or κ-receptors, switches pulmonary C-fiber-mediated rapid shallow breathing into an apnea in anesthetized rats.阿片μ受体的激活而非δ或κ受体的激活可将麻醉大鼠肺部 C 纤维介导的快速浅呼吸转换为呼吸暂停。
Respir Physiol Neurobiol. 2012 Sep 30;183(3):211-7. doi: 10.1016/j.resp.2012.06.032. Epub 2012 Jul 11.
3
8-OH-DPAT abolishes the pulmonary C-fiber-mediated apneic response to fentanyl largely via acting on 5HT1A receptors in the nucleus tractus solitarius.8-OH-DPAT 主要通过作用于孤束核中的 5-HT1A 受体而消除芬太尼引起的肺 C 纤维介导的呼吸暂停反应。
Am J Physiol Regul Integr Comp Physiol. 2012 Aug 15;303(4):R449-58. doi: 10.1152/ajpregu.00016.2012. Epub 2012 Jun 13.
4
Cardio-respiratory reflexes evoked by phenylbiguanide in rats involve vagal afferents which are not sensitive to capsaicin.苯丁胍诱发大鼠的心肺反射涉及不敏感于辣椒素的迷走传入纤维。
Acta Physiol (Oxf). 2010 Sep;200(1):87-95. doi: 10.1111/j.1748-1716.2010.02105.x. Epub 2010 Mar 10.
5
Mechanisms of eosinophil major basic protein-induced hyperexcitability of vagal pulmonary chemosensitive neurons.嗜酸性粒细胞主要碱性蛋白诱导迷走神经肺化学敏感神经元兴奋性增高的机制
Am J Physiol Lung Cell Mol Physiol. 2009 Mar;296(3):L453-61. doi: 10.1152/ajplung.90467.2008. Epub 2009 Jan 9.
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Activation of 5-hydroxytryptamine type 3 receptor-expressing C-fiber vagal afferents inhibits retrotrapezoid nucleus chemoreceptors in rats.激活表达5-羟色胺3型受体的C纤维迷走神经传入纤维可抑制大鼠延髓后外侧网状核化学感受器。
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Central pathways of pulmonary and lower airway vagal afferents.肺和下呼吸道迷走神经传入的中枢通路。
J Appl Physiol (1985). 2006 Aug;101(2):618-27. doi: 10.1152/japplphysiol.00252.2006. Epub 2006 Apr 27.
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Understanding nausea and vomiting in advanced cancer.了解晚期癌症患者的恶心与呕吐。
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Functional and histological studies of the vagus nerve and its branches to the heart, lungs and abdominal viscera in the cat.猫迷走神经及其至心脏、肺和腹部脏器分支的功能与组织学研究
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Functional morphology and physiological properties of bronchopulmonary C-fiber afferents.支气管肺C纤维传入神经的功能形态学和生理学特性
Anat Rec A Discov Mol Cell Evol Biol. 2003 Jan;270(1):17-24. doi: 10.1002/ar.a.10005.

异氟烷通过抑制麻醉大鼠 5-HT3 受体功能抑制苯并胍胺介导的支气管肺 C 纤维介导的呼吸暂停反应。

Isoflurane inhibits bronchopulmonary C-fiber-mediated apneic response to phenylbiguanide by depressing 5-HT3 receptor function in anesthetized rats.

机构信息

Pathophysiology Program, Lovelace Respiratory Research Institute, 2425 Ridgecrest Drive, SE, Albuquerque, NM 87108, United States.

出版信息

Neurosci Lett. 2013 Sep 27;552:1-4. doi: 10.1016/j.neulet.2013.07.024. Epub 2013 Jul 26.

DOI:10.1016/j.neulet.2013.07.024
PMID:23896531
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3857219/
Abstract

A previous study by the authors has shown that isoflurane (ISO), a commonly used volatile anesthetic, has an excitatory effect on bronchopulmonary C-fibers (PCFs). Since selective stimulation of PCFs by action on local 5-HT3 receptors could evoke an apnea, this current study addresses whether inhalation of ISO would facilitate the PCF 5-HT3 receptor-mediated apneic response and, if so, how. In anesthetized and spontaneously breathing rats, inhalation of 5% ISO markedly inhibited the apneic response to intra-atrium injection of phenylbiguanide (PBG, 25 μg/kg), a 5-HT3 receptor agonist, which was contrary to the hypothesis. Extracellular recording of the nodose ganglion neurons in anesthetized, paralyzed and ventilated rats revealed that ISO attenuated the PBG-elicited excitation of pulmonary C neurons. Furthermore, using the patch clamp technique, it was found that ISO depressed the PBG-induced inward current of the pulmonary C neurons labeled with 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) instilled previously into the lungs. These results suggest that ISO inhibits PCF 5-HT3 channel functions, and thereby attenuates PCF excitatory response to PBG, likely contributing to the diminution of the PBG-induced apnea by ISO in rats.

摘要

作者之前的一项研究表明,异氟醚(ISO)是一种常用的挥发性麻醉剂,对支气管肺 C 纤维(PCF)具有兴奋作用。由于局部 5-HT3 受体的作用选择性刺激 PCF 可引起呼吸暂停,因此本研究旨在探讨吸入 ISO 是否会促进 PCF 5-HT3 受体介导的呼吸暂停反应,如果是,其机制如何。在麻醉和自主呼吸的大鼠中,吸入 5%的 ISO 可显著抑制心房内注射苯并胍(PBG,25μg/kg)引起的呼吸暂停反应,这与假设相反。在麻醉、麻痹和通气的大鼠的神经节神经元的细胞外记录显示,ISO 减弱了 PBG 诱发的肺 C 神经元的兴奋。此外,使用膜片钳技术,发现 ISO 抑制了先前注入肺内并用 1,1'-二辛基-3,3,3',3'-四甲基吲哚羰花青高氯酸盐(DiI)标记的肺 C 神经元中 PBG 诱导的内向电流。这些结果表明,ISO 抑制 PCF 5-HT3 通道功能,从而减弱 PCF 对 PBG 的兴奋反应,可能有助于 ISO 减轻大鼠中 PBG 诱导的呼吸暂停。