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钾离子通道开放和钠钾ATP酶活性在沙丁胺醇诱导的气道舒张中的作用。

Role of K+ channel opening and Na(+)-K+ ATPase activity in airway relaxation induced by salbutamol.

作者信息

Tamaoki J, Tagaya E, Chiyotani A, Yamawaki I, Konno K

机构信息

First Department of Medicine, Tokyo Women's Medical College, Japan.

出版信息

Life Sci. 1994;55(11):PL217-23. doi: 10.1016/0024-3205(94)90050-7.

Abstract

To determine the role of K+ channel opening and Na(+)-K+ ATPase activity in the beta-adrenoceptor-mediated relaxation of airway smooth muscle, we studied canine bronchial segments under isometric conditions in vitro. Relaxant responses to salbutamol were not altered by glibenclamide or apamin but inhibited by charybdotoxin, where significant inhibition was observed only at salbutamol concentrations of less than 10(-6) M. In contrast, only the relaxations induced by salbutamol at 3 x 10(-6) M and greater were sensitive to ouabain. Relaxations produced by low and high concentrations of salbutamol were selectively attenuated by charybdotoxin and ouabain, respectively, in a concentration-dependent manner. These results suggest that both Ca(2+)-activated K+ channel and Na(+)-K+ ATPase may be operative in the airway relaxation induced by low and high concentrations of the beta-adrenergic agonist, respectively.

摘要

为了确定钾离子通道开放和钠钾ATP酶活性在β肾上腺素能受体介导的气道平滑肌舒张中的作用,我们在体外等长条件下研究了犬支气管节段。格列本脲或阿帕明未改变对沙丁胺醇的舒张反应,但被大蝎毒素抑制,仅在沙丁胺醇浓度低于10⁻⁶ M时观察到显著抑制。相比之下,仅3×10⁻⁶ M及更高浓度的沙丁胺醇诱导的舒张对哇巴因敏感。低浓度和高浓度沙丁胺醇产生的舒张分别被大蝎毒素和哇巴因以浓度依赖的方式选择性减弱。这些结果表明,钙激活钾离子通道和钠钾ATP酶可能分别在低浓度和高浓度β肾上腺素能激动剂诱导的气道舒张中起作用。

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