Canning Brendan J
Johns Hopkins Asthma and Allergy Center, Baltimore, MD 21224, USA.
J Appl Physiol (1985). 2006 Sep;101(3):971-85. doi: 10.1152/japplphysiol.00313.2006. Epub 2006 May 25.
Autonomic nerves in most mammalian species mediate both contractions and relaxations of airway smooth muscle. Cholinergic-parasympathetic nerves mediate contractions, whereas adrenergic-sympathetic and/or noncholinergic parasympathetic nerves mediate relaxations. Sympathetic-adrenergic innervation of human airway smooth muscle is sparse or nonexistent based on histological analyses and plays little or no role in regulating airway caliber. Rather, in humans and in many other species, postganglionic noncholinergic parasympathetic nerves provide the only relaxant innervation of airway smooth muscle. These noncholinergic nerves are anatomically and physiologically distinct from the postganglionic cholinergic parasympathetic nerves and differentially regulated by reflexes. Although bronchopulmonary vagal afferent nerves provide the primary afferent input regulating airway autonomic nerve activity, extrapulmonary afferent nerves, both vagal and nonvagal, can also reflexively regulate autonomic tone in airway smooth muscle. Reflexes result in either an enhanced activity in one or more of the autonomic efferent pathways, or a withdrawal of baseline cholinergic tone. These parallel excitatory and inhibitory afferent and efferent pathways add complexity to autonomic control of airway caliber. Dysfunction or dysregulation of these afferent and efferent nerves likely contributes to the pathogenesis of obstructive airways diseases and may account for the pulmonary symptoms associated with extrapulmonary disorders, including gastroesophageal reflux disease, cardiovascular disease, and rhinosinusitis.
在大多数哺乳动物物种中,自主神经可介导气道平滑肌的收缩和舒张。胆碱能副交感神经介导收缩,而肾上腺素能交感神经和/或非胆碱能副交感神经介导舒张。基于组织学分析,人类气道平滑肌的交感肾上腺素能神经支配稀疏或不存在,在调节气道管径方面作用很小或不起作用。相反,在人类和许多其他物种中,节后非胆碱能副交感神经是气道平滑肌唯一的舒张性神经支配。这些非胆碱能神经在解剖学和生理学上与节后胆碱能副交感神经不同,并受到反射的差异性调节。尽管支气管肺迷走传入神经是调节气道自主神经活动的主要传入输入,但肺外传入神经,包括迷走神经和非迷走神经,也可反射性调节气道平滑肌的自主张力。反射可导致一种或多种自主传出通路的活动增强,或基线胆碱能张力的降低。这些平行的兴奋性和抑制性传入和传出通路增加了气道管径自主控制的复杂性。这些传入和传出神经的功能障碍或调节异常可能导致阻塞性气道疾病的发病机制,并可能解释与肺外疾病相关的肺部症状,包括胃食管反流病、心血管疾病和鼻窦炎。