Tamoxifen inhibits Ca2+ uptake by the cardiac sarcoplasmic reticulum

被引:0
|
作者
Margaret E. Kargacin
Zenobia Ali
Christopher A. Ward
Natashka S. Pollock
Gary J. Kargacin
机构
[1] Department of Physiology and Biophysics,
[2] University of Calgary,undefined
[3] 3330 Hospital Drive NW,undefined
[4] Calgary,undefined
[5] Alberta T2N 4N1,undefined
[6] Canada,undefined
[7] Department of Physiology,undefined
[8] Queens University,undefined
[9] Kingston,undefined
[10] Ontario K7L 3N6,undefined
[11] Canada,undefined
来源
Pflügers Archiv | 2000年 / 440卷 / 4期
关键词
Ca2+-ATPase Cardiac myocytes Fluo3 Fura-2 Membrane vesicles;
D O I
10.1007/s004240000318
中图分类号
学科分类号
摘要
Ca2+ transients in isolated cardiac ventricular myocytes and the amount of Ca2+ that could be released from the sarcoplasmic reticulum (SR) in these cells by caffeine were reduced in the presence of tamoxifen. To examine the effects of tamoxifen on the cardiac muscle SR directly, isolated SR vesicles and fluorimetry methods were used to measure the uptake of Ca2+ by the SR and the ATPase activity of the SR Ca2+ pump. SR Ca2+ uptake was inhibited by tamoxifen at concentrations greater than 2.4 µM. Half-maximal inhibition was seen at approximately 5 µM. Inhibition of uptake was not due to the development of a substantial tamoxifen-dependent leak of Ca2+ from the SR or to a direct inhibitory effect of tamoxifen on the ATPase activity of the SR Ca2+ pump. In addition to its effect on SR Ca2+ uptake, tamoxifen also reduced the rate at which stored Ca2+ could be released from the SR by the Ca2+ ionophore 4-bromo A23187. Our results are consistent with the hypothesis that tamoxifen inhibits an ion current that accompanies Ca2+ movement across the SR membrane. This possibility is also consistent with the known inhibitory action of tamoxifen on some types of Cl– and K+ channels.
引用
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页码:573 / 579
页数:6
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