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艾森曼格综合征的气道结构与功能

Airway structure and function in Eisenmenger's syndrome.

作者信息

McKay K O, Johnson P R, Black J L, Glanville A R, Armour C L

机构信息

Departments of Pharmacology and Pharmacy, University of Sydney; and the Cardiopulmonary Transplant Unit, St. Vincent's Hospital, Darlinghurst, New South Wales, Australia.

出版信息

Am J Respir Crit Care Med. 1998 Oct;158(4):1245-52. doi: 10.1164/ajrccm.158.4.9711105.

Abstract

The responsiveness of airways from patients with Eisenmenger's syndrome (n = 5) was compared with that in airways from organ donors (n = 10). Enhanced contractile responses to cholinergic stimulation were found in airways from patients with Eisenmenger's syndrome. The maximal responses to acetylcholine, carbachol, and parasympathetic nerve stimulation in airway tissue from these patients were 221%, 139%, and 152%, respectively, of the maximal responses obtained in donor tissue. Further, relaxation responses to isoproterenol and levocromakalim were absent (n = 2) or markedly impaired (n = 3) in airways from patients with Eisenmenger's syndrome. This attenuated relaxation response was nonspecific in that it was also absent after vasoactive intestinal peptide, sodium nitroprusside, papaverine, and electrical field application. These observations can most likely be explained by a decrease in intrinsic smooth muscle tone, as precontraction of airways revealed relaxation responses that were equivalent to those obtained in donor tissues. Morphometric analysis of tissues used for the functional studies revealed no differences in the airway dimensions (internal perimeter) or airway wall components (e.g., smooth muscle, cartilage) or total area to explain these observations. Although the mechanism for this observed decrease in intrinsic airway smooth muscle tone is not certain, it may be due to alteration in the substructure of the airway wall or, alternatively, may result from the continued release of depressant factors in the vicinity of the smooth muscle which permanently alters smooth muscle responsiveness.

摘要

将艾森曼格综合征患者(n = 5)的气道反应性与器官供体的气道反应性(n = 10)进行了比较。发现艾森曼格综合征患者的气道对胆碱能刺激的收缩反应增强。这些患者气道组织中对乙酰胆碱、卡巴胆碱和副交感神经刺激的最大反应分别为供体组织中最大反应的221%、139%和152%。此外,艾森曼格综合征患者的气道对异丙肾上腺素和左西孟旦的舒张反应缺失(n = 2)或明显受损(n = 3)。这种减弱的舒张反应是非特异性的,因为在应用血管活性肠肽、硝普钠、罂粟碱和电场后也不存在。这些观察结果很可能可以用内在平滑肌张力降低来解释,因为气道预收缩显示出与供体组织中获得的舒张反应相当的舒张反应。对用于功能研究的组织进行形态计量分析发现,气道尺寸(内周长)、气道壁成分(如平滑肌、软骨)或总面积没有差异来解释这些观察结果。虽然观察到的气道内在平滑肌张力降低的机制尚不确定,但可能是由于气道壁亚结构的改变,或者可能是由于平滑肌附近持续释放抑制因子,从而永久性地改变了平滑肌反应性。

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