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皮质类固醇对人呼吸道黏液糖蛋白体外分泌的影响。

The effects of corticosteroids on mucous glycoprotein secretion from human airways in vitro.

作者信息

Marom Z, Shelhamer J, Alling D, Kaliner M

出版信息

Am Rev Respir Dis. 1984 Jan;129(1):62-5. doi: 10.1164/arrd.1984.129.1.62.

Abstract

In order to examine the mechanisms by which corticosteroids may benefit some patients with bronchorrhea, cultured human airways releasing [3H]glucosamine labeled mucous glycoproteins were exposed to corticosteroids, and mucus release was examined. Both dexamethasone and methylprednisolone produced dose-related suppression of the spontaneous release of radiolabeled mucous glycoproteins. The inhibitory effects of dexamethasone were maximal after 18 to 24 h and returned to control levels by 34 h. In order to study the effects of dexamethasone on stimulated mucus release, airways were exposed to dexamethasone and to the mucus secretagogues, histamine or 5-monohydroxyeicosatetraenoic acid. Both of these secretagogues stimulated radiolabeled mucous glycoprotein release from airways that had never been exposed to corticosteroids, as well as in a reduced fashion from corticosteroid-treated airways. The reduced mucus release caused by secretagogues from dexamethasone-treated airways appeared to reflect a lowered baseline secretion rate rather than a specific inhibition of either secretagogue.

摘要

为了研究皮质类固醇可能使一些支气管溢液患者受益的机制,将释放[3H]氨基葡萄糖标记的粘液糖蛋白的培养人气道暴露于皮质类固醇,并检测粘液释放情况。地塞米松和甲泼尼龙均产生了与剂量相关的对放射性标记粘液糖蛋白自发释放的抑制作用。地塞米松的抑制作用在18至24小时后达到最大,并在34小时时恢复到对照水平。为了研究地塞米松对刺激的粘液释放的影响,将气道暴露于地塞米松以及粘液促分泌剂组胺或5-单羟基二十碳四烯酸。这两种促分泌剂均刺激了从未暴露于皮质类固醇的气道中放射性标记的粘液糖蛋白释放,以及以降低的方式刺激了经皮质类固醇处理的气道中的释放。地塞米松处理的气道中促分泌剂引起的粘液释放减少似乎反映了基线分泌率降低,而不是对任何一种促分泌剂的特异性抑制。

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