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氧化性上皮损伤会导致人类外周气道反应过度。

Oxidative epithelial damage produces hyperresponsiveness of human peripheral airways.

作者信息

Hulsmann A R, Raatgeep H R, den Hollander J C, Stijnen T, Saxena P R, Kerrebijn K F, de Jongste J C

机构信息

Department of Pediatrics, Erasmus University, Rotterdam, The Netherlands.

出版信息

Am J Respir Crit Care Med. 1994 Feb;149(2 Pt 1):519-25. doi: 10.1164/ajrccm.149.2.8306055.

Abstract

The epithelium probably modulates airway smooth muscle responsiveness by producing relaxing factors, by inactivating agonists, or by acting as a physical barrier. In isolated airway strips, however, only a limited modulatory role of the epithelium has been found, and this may well be due to shortcomings of this airway model. The present study compares the modulatory role of the airway epithelium in human airway tubes and strips. In addition, since oxygen radicals may contribute to epithelial damage in asthma, oxidative damage to the airway epithelium was induced with luminally applied hydrogen peroxide (H2O2), and changes in responsiveness to the agonists histamine, methacholine, and salbutamol were measured. To examine whether intact epithelium acts as a barrier to histamine, the histamine concentration in the organ bath was measured in tubes with intact and damaged epithelium stimulated from the mucosal side. In airway strips, no differences in responsiveness were found between intact and epithelium-denuded airways for any of the three agonists. In contrast, the sensitivity of airway tubes to both histamine and methacholine was significantly lower with mucosal stimulation than with serosal stimulation (-log EC50: 4.87 and 4.92 versus 5.87 and 5.45 for histamine and methacholine, respectively, p < 0.001). No difference was found between the sensitivity to salbutamol of mucosally and serosally stimulated airways (-log EC50: 6.19 and 6.20, respectively). The modulation of the sensitivity to contractile agonists by the epithelium increased with increasing airway size, and was abolished after treatment with H2O2.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

上皮组织可能通过产生舒张因子、使激动剂失活或作为物理屏障来调节气道平滑肌反应性。然而,在离体气道条中,仅发现上皮组织具有有限的调节作用,这很可能是由于该气道模型存在缺陷。本研究比较了气道上皮组织在人气管和气道条中的调节作用。此外,由于氧自由基可能导致哮喘中的上皮损伤,因此通过向管腔内应用过氧化氢(H2O2)诱导气道上皮的氧化损伤,并测量对组胺、乙酰甲胆碱和沙丁胺醇等激动剂反应性的变化。为了研究完整上皮组织是否对组胺起屏障作用,在从黏膜侧刺激的完整上皮和受损上皮的气管中测量器官浴中的组胺浓度。在气道条中,对于三种激动剂中的任何一种,完整气道和去上皮气道之间的反应性均未发现差异。相比之下,黏膜刺激时气道对组胺和乙酰甲胆碱的敏感性明显低于浆膜刺激时(组胺和乙酰甲胆碱的-log EC50分别为4.87和4.92,而浆膜刺激时为5.87和5.45,p < 0.001)。黏膜刺激和浆膜刺激的气道对沙丁胺醇的敏感性之间未发现差异(-log EC50分别为6.19和6.20)。上皮组织对收缩性激动剂敏感性的调节作用随气道大小增加而增强,并且在用H2O2处理后消失。(摘要截短于250字)

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