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人支气管上皮衍生抑制因子

Epithelium-derived inhibitory factor in human bronchus.

作者信息

Fernandes L B, Preuss J M, Paterson J W, Goldie R G

机构信息

Department of Pharmacology, University of Western Australia, Perth.

出版信息

Eur J Pharmacol. 1990 Oct 23;187(3):331-6. doi: 10.1016/0014-2999(90)90360-i.

Abstract

The potencies of histamine and methacholine were significantly increased by approximately 2- and 5-fold respectively in human non-diseased isolated bronchi on removal of the epithelium. In contrast, no increases in spasmogen potency were observed following epithelium removal in bronchi obtained from a sample of asthmatic human lung. The failure of epithelium removal to increase asthmatic bronchial sensitivity to histamine may have been due to a reduction in the release of an epithelium-derived inhibitory factor (EpDIF) resulting from disease-induced epithelial damage. A co-axial bioassay system in which endothelium-denuded rat aorta was used as the assay tissue was used to detect the release of a vasorelaxant EpDIF from human bronchial tissue. Histamine (100 microM) and methacholine (25 microM), in the presence of indomethacin (5 microM), reduced phenylephrine-induced tone in endothelium-denuded rat aorta in co-axial assemblies by 75 +/- 11 and 67 +/- 9% respectively. Removal of the bronchial epithelium abolished these responses, indicating that they were mediated by an EpDIF. It is possible that human airway smooth muscle is sensitive to this vasorelaxant EpDIF and that the absence of the source of this factor following epithelium removal caused the increases in sensitivity to spasmogens. Alternatively, the human bronchial epithelium may also release an EpDIF selective for airway smooth muscle.

摘要

在去除上皮后,人非病变离体支气管中组胺和乙酰甲胆碱的效力分别显著增加了约2倍和5倍。相比之下,从哮喘患者肺样本中获取的支气管在去除上皮后,未观察到致痉剂效力增加。去除上皮未能增加哮喘支气管对组胺的敏感性,可能是由于疾病引起的上皮损伤导致上皮衍生抑制因子(EpDIF)释放减少。使用以去内皮大鼠主动脉为检测组织的同轴生物检测系统,来检测人支气管组织中血管舒张性EpDIF的释放。在吲哚美辛(5 microM)存在的情况下,组胺(100 microM)和乙酰甲胆碱(25 microM)分别使同轴组件中去内皮大鼠主动脉的苯肾上腺素诱导张力降低了75±11%和67±9%。去除支气管上皮消除了这些反应,表明它们是由EpDIF介导的。有可能人气道平滑肌对这种血管舒张性EpDIF敏感,并且去除上皮后该因子来源的缺失导致了对致痉剂敏感性的增加。或者,人支气管上皮也可能释放对气道平滑肌有选择性的EpDIF。

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