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气道上皮衍生的舒张因子:是臆想、现实还是幼稚?

Airway epithelium-derived relaxing factor: myth, reality, or naivety?

机构信息

Department of Pharmacology and Pharmacy, University of Hong Kong, Hong Kong, China.

出版信息

Am J Physiol Cell Physiol. 2013 May 1;304(9):C813-20. doi: 10.1152/ajpcell.00013.2013. Epub 2013 Jan 16.

Abstract

The presence of a healthy epithelium can moderate the contraction of the underlying airway smooth muscle. This is, in part, because epithelial cells generate inhibitory messages, whether diffusible substances, electrophysiological signals, or both. The epithelium-dependent inhibitory effect can be tonic (basal), synergistic, or evoked. Rather than a unique epithelium-derived relaxing factor (EpDRF), several known endogenous bronchoactive mediators, including nitric oxide and prostaglandin E2, contribute. The early concept that EpDRF diffuses all the way through the subepithelial layers to directly relax the airway smooth muscle appears unlikely. It is more plausible that the epithelial cells release true messenger molecules, which alter the production of endogenous substances (nitric oxide and/or metabolites of arachidonic acid) by the subepithelial layers. These substances then diffuse to the airway smooth muscle cells, conveying epithelium dependency.

摘要

健康的上皮组织可以调节气道平滑肌的收缩。这部分是因为上皮细胞会产生抑制性信号,无论是扩散物质、电生理信号还是两者兼有。上皮组织依赖性的抑制作用可以是紧张性的(基础的)、协同性的或诱发的。并非有一种独特的上皮衍生性舒张因子(EpDRF),几种已知的内源性支气管活性介质,包括一氧化氮和前列腺素 E2,也有贡献。早期的概念认为 EpDRF 会扩散穿过黏膜下层,直接松弛气道平滑肌,这似乎不太可能。更有可能的是,上皮细胞释放真正的信使分子,改变黏膜下层产生内源性物质(一氧化氮和/或花生四烯酸的代谢物)的方式。这些物质随后扩散到气道平滑肌细胞,传递上皮依赖性。

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