...
首页> 外文期刊>Molecular pain >TRPM8 mechanism of autonomic nerve response to cold in respiratory airway
【24h】

TRPM8 mechanism of autonomic nerve response to cold in respiratory airway

机译:自主神经对呼吸道寒冷的反应机制

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Breathing cold air without proper temperature exchange can induce strong respiratory autonomic responses including cough, airway constriction and mucosal secretion, and can exacerbate existing asthma conditions and even directly trigger an asthma attack. Vagal afferent fiber is thought to be involved in the cold-induced respiratory responses through autonomic nerve reflex. However, molecular mechanisms by which vagal afferent fibers are excited by cold remain unknown. Using retrograde labeling, immunostaining, calcium imaging, and electrophysiological recordings, here we show that a subpopulation of airway vagal afferent nerves express TRPM8 receptors and that activation of TRPM8 receptors by cold excites these airway autonomic nerves. Thus activation of TRPM8 receptors may provoke autonomic nerve reflex to increase airway resistance. This putative autonomic response may be associated with cold-induced exacerbation of asthma and other pulmonary disorders, making TRPM8 receptors a possible target for prevention of cold-associated respiratory disorders.
机译:呼吸冷空气而没有适当的温度交换会引起强烈的呼吸自主反应,包括咳嗽,气道收缩和粘膜分泌,并可能加剧现有的哮喘病,甚至直接引发哮喘发作。迷走神经传入纤维被认为通过自主神经反射参与了感冒诱发的呼吸反应。然而,迷走神经传入纤维被冷激发的分子机制仍然未知。使用逆行标记,免疫染色,钙成像和电生理学记录,此处我们显示气道迷走神经传入神经的亚群表达TRPM8受体,而TRPM8受体受冷激活会激发这些气道自主神经。因此,激活TRPM8受体可能会引起自主神经反射,从而增加气道阻力。这种假定的自主反应可能与感冒诱发的哮喘发作加重和其他肺部疾病有关,使TRPM8受体成为预防感冒相关呼吸系统疾病的可能靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号