首页> 外文期刊>The Journal of Physiology >Synergistic interactions between airway afferent nerve subtypes regulating the cough reflex in guinea-pigs.
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Synergistic interactions between airway afferent nerve subtypes regulating the cough reflex in guinea-pigs.

机译:调节豚鼠咳嗽反射的气道传入神经亚型之间的协同相互作用。

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Cough initiated from the trachea and larynx in anaesthetized guinea-pigs is mediated by capsaicin-insensitive, mechanically sensitive vagal afferent neurones. Tachykinin-containing, capsaicin-sensitive C-fibres also innervate the airways and have been implicated in the cough reflex. Capsaicin-sensitive nerves act centrally and synergistically to modify reflex bronchospasm initiated by airway mechanoreceptor stimulation. The hypothesis that polymodal mechanoreceptors and capsaicin-sensitive afferent nerves similarly interact centrally to regulate coughing was addressed in this study. Cough was evoked from the tracheal mucosa either electrically (16 Hz, 10 s trains, 1-10 V) or by citric acid (0.001-2 m). Neither capsaicin nor bradykinin evoked a cough when applied to the trachea of anaesthetized guinea-pigs, but they substantially reduced the electrical threshold for initiating the cough reflex. The TRPV1 receptor antagonist capsazepine prevented the increased cough sensitivity induced by capsaicin. These effects of topically applied capsaicin and bradykinin were not due to interactions between afferent nerve subtypes within the tracheal wall or a direct effect on the cough receptors, as they were mimicked by nebulizing 1 mg ml(-1) bradykinin into the lower airways and by microinjecting 0.5 nmol capsaicin into nucleus of the solitary tract (nTS). Citric acid-induced coughing was also potentiated by inhalation of bradykinin. The effects of tracheal capsaicin challenge on cough were mimicked by microinjecting substance P (0.5-5 nmol) into the nTS and prevented by intracerebroventricular administration (20 nmol h(-1)) of the neurokinin receptor antagonists CP99994 or SB223412. Tracheal application of these antagonists was without effect. C-fibre activation may thus sensitize the cough reflex via central mechanisms.
机译:麻醉的豚鼠的气管和喉头引发的咳嗽是由对辣椒素不敏感的,机械敏感的迷走神经传入神经元介导的。含有速激肽的,对辣椒素敏感的C纤维也支配气道,并与咳嗽反射有关。辣椒素敏感的神经在中央和协同作用下改变由气道机械感受器刺激引起的反射性支气管痉挛。在这项研究中提出了多峰机械感受器和辣椒素敏感传入神经类似地集中调节咳嗽的假设。用电(16 Hz,10 s串,1-10 V)或柠檬酸(0.001-2 m)从气管粘膜引起咳嗽。当将辣椒素或缓激肽应用于麻醉的豚鼠的气管时,都不会引起咳嗽,但它们显着降低了开始咳嗽反射的电阈值。 TRPV1受体拮抗剂辣椒碱可防止辣椒素引起的咳嗽敏感性增加。局部应用辣椒素和缓激肽的这些作用不是由于气管壁内传入神经亚型之间的相互作用,也不是对咳嗽受体的直接作用,因为它们是通过将1 mg ml(-1)缓激肽雾化到下呼吸道并通过将0.5 nmol辣椒素微注​​射​​到孤立道(nTS)的核中。吸入缓激肽也可增强柠檬酸引起的咳嗽。气管辣椒素激发​​对咳嗽的影响可通过将P(0.5-5 nmol)物质微注射到nTS中来模拟,并通过脑室内施用(20 nmol h(-1))神经激肽受体拮抗剂CP99994或SB223412来预防。这些拮抗剂的气管施用没有效果。因此,C纤维激活可能通过中枢机制使咳嗽反射更为敏感。

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