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阴离子转运抑制剂二异丙基氟磷酸(DIDS)可从肝微粒体中释放钙离子。

Inhibitor of anion transport, DIDS, releases Ca2+ from hepatic microsomes.

作者信息

Kimura S, Robison B C, Kraus-Friedmann N

机构信息

Department of Physiology and Cell Biology, University of Texas Health Science Center, School of Medicine, Houston 77225.

出版信息

Biochem Biophys Res Commun. 1988 Feb 29;151(1):396-401. doi: 10.1016/0006-291x(88)90606-7.

Abstract

Addition of 4,4'-diisothiocyanostilbene-2, 2'-disulfonic acid (DIDS) to Ca2+ loaded hepatic microsomal vesicles evoked a dose-dependent release of the accumulated Ca2+. Ca2+ uptake was also inhibited. The effects of DIDS do not seem to be due to the inhibitions of either Cl- or proton fluxes. The results indicate that DIDS inhibits Ca2+ uptake and releases Ca2+ by inhibiting the Ca2+-ATPase and the formation of the phosphorylated intermediate of the enzyme, and that it might interact with a specific site on the vesicle which is involved in the translocation of Ca2+ across the microsomal and mitochondrial membranes.

摘要

向负载Ca2+的肝微粒体囊泡中添加4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)会引起累积Ca2+的剂量依赖性释放。Ca2+摄取也受到抑制。DIDS的作用似乎并非由于对Cl-或质子通量的抑制。结果表明,DIDS通过抑制Ca2+-ATP酶及其磷酸化中间体的形成来抑制Ca2+摄取并释放Ca2+,并且它可能与囊泡上参与Ca2+跨微粒体和线粒体膜转运的特定位点相互作用。

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