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胰岛素对大鼠红细胞中钠/氢反向转运体的调节作用。

Insulin modulation of Na/H antiport in rat red blood cells.

作者信息

Rizvi S I, Incerpi S, Luly P

机构信息

Department of Biochemistry, University of Allahabad, India.

出版信息

Indian J Biochem Biophys. 1994 Apr;31(2):127-30.

PMID:7927433
Abstract

Red blood cells have been shown to possess specific insulin receptors, with characteristics similar to the receptors of typical target cells. The present work was carried out to study the modulation of amiloride sensitive Na/H antiport by insulin on rat red blood cells. The activity of the Na/H antiport was determined by a new technique which involves the measurement of the fluorescence of 2',7'-bis(2-carboxyethyl)-5,6-carboxyfluorescein (BCECF) loaded rbc's as function of their intracellular pH (pHi). Our results show that the antiport in red blood cells displays the same behaviour as in other cells and it is inhibited by amiloride. Insulin stimulates the antiport with a dose-dependence similar to other typical insulin effects: a maximum at 10 nM and a smaller effect at higher and lower hormone concentrations. Insulin effect on the antiport was completely abolished by amiloride (0.1 mM) and significantly inhibited by ouabain (1 mM) showing, also in red blood cells, the strict dependence of the Na/H antiport on the functioning of the Na pump.

摘要

已证实红细胞具有特定的胰岛素受体,其特性与典型靶细胞的受体相似。开展本研究是为了探讨胰岛素对大鼠红细胞中氨氯地平敏感的钠/氢逆向转运体的调节作用。钠/氢逆向转运体的活性通过一项新技术测定,该技术涉及测量负载2',7'-双(2-羧乙基)-5,6-羧基荧光素(BCECF)的红细胞的荧光,并将其作为细胞内pH(pHi)的函数。我们的结果表明,红细胞中的逆向转运体表现出与其他细胞相同的行为,且受氨氯地平抑制。胰岛素以类似于其他典型胰岛素效应的剂量依赖性刺激逆向转运体:在10 nM时达到最大值,在更高和更低的激素浓度下效应较小。氨氯地平(0.1 mM)完全消除了胰岛素对逆向转运体的作用,哇巴因(1 mM)显著抑制了该作用,这也表明在红细胞中,钠/氢逆向转运体严格依赖于钠泵的功能。

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