SK-AND-F 96365, A RECEPTOR-MEDIATED CALCIUM ENTRY INHIBITOR, INHIBITS CALCIUM RESPONSES TO ENDOTHELIN-1 IN NG108-15 CELLS

被引:36
作者
CHAN, J
GREENBERG, DA
机构
[1] UNIV CALIF SAN FRANCISCO,DIV CLIN PHARMACOL & THERAPEUT,SAN FRANCISCO,CA 94110
[2] SAN FRANCISCO GEN HOSP,SAN FRANCISCO,CA 94110
关键词
D O I
10.1016/0006-291X(91)90658-T
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endothelin-1 increases intracellular Ca2+ in NG108-15 cells by mobilizing Ca2+ from internal stores and by activating Ca2+ entry through dihydropyridine-sensitive, voltagegated channels and another, unidentified route. Since SK&F 96365 has recently been reported to inhibit receptor-mediated Ca2+ entry in other systems, we examined its effect on intracellular Ca2+ responses to endothelin-1, measured with the fluorescent Ca2+ indicator fura-2, in NG108-15 cells. SK&F 96365 (30 μM) reduced both dihydropyridine-insensitive (peak) and dihydropyridine-sensitive (plateau) components of intracellular Ca2+ responses to 5 nM endothelin-1. In the presence of 100 nM nimodipine, which blocks dihydropyridine-sensitive channels, SK&F 96365 caused concentration-dependent inhibition of Ca2+ responses to 5 nM endothelin-1, with half-maximal inhibition at 16 μM. These findings support a role for receptor-mediated Ca2+ entry in neurocellular Ca2+ responses to endothelin-1. © 1991.
引用
收藏
页码:1141 / 1146
页数:6
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