Chloride channel blockers inhibit Ca2+ uptake by the smooth muscle sarcoplasmic reticulum

被引:50
作者
Pollock, NS [1 ]
Kargacin, ME [1 ]
Kargacin, GJ [1 ]
机构
[1] Univ Calgary, Dept Physiol & Biophys, Calgary, AB T2N 4N1, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0006-3495(98)77617-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Despite the fact that Ca2+ transport into the sarcoplasmic reticulum (SR) of muscle cells is electrogenic, a potential difference is not maintained across the SR membrane. To achieve electroneutrality, compensatory charge movement must occur during Ca2+ uptake. To examine the role of Cl- in this charge movement in smooth muscle cells, Ca2+ transport into the SR of saponin-permeabilized smooth muscle cells was measured in the presence of various Cl- channel blockers or when l(-), Br-, or SO42- was substituted for Cl-. Calcium uptake was inhibited in a dose-dependent manner by 5-nitro-2-(3-phenylpropylamino) benzoic acid (NPPB) and by indanyioxyacetic acid 94 (R(+)-IAA-94), but not by niflumic acid or 4,4'-dinitrostilbene-2,2'-disulfonic acid (DNDS). Smooth muscle SR Ca2+ uptake was also partially inhibited by the substitution of SO42- for Cl-, but not when Cl- was replaced by l(-) or Br-. Neither NPPB nor R(+)-IAA-94 inhibited Ca2+ uptake into cardiac muscle SR vesicles at concentrations that maximally inhibited uptake in smooth muscle cells. These results indicate that Cl- movement is important for charge compensation in smooth muscle cells and that the Cl- channel or channels involved are different in smooth and cardiac muscle cells.
引用
收藏
页码:1759 / 1766
页数:8
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