Nicardipine inhibits N-type calcium channels in dbcAMP-differentiated neuroblastoma x glioma hybrid cells (NG 108-15 cells)

被引:0
作者
Li, SN [1 ]
Bräter, M [1 ]
Andreas, K [1 ]
机构
[1] Dresden Univ Technol, Inst Pharmacol & Toxicol, D-01109 Dresden, Germany
来源
ACTA PHARMACOLOGICA SINICA | 1999年 / 20卷 / 02期
关键词
dihydropyridines; nicardipine; nifedipine; calcium channels; Fura-2; cyclic AMP; NG; 108-15; cells;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
AIM: To investigate the possibility of dihydropyridine inhibition of N-type calcium channels. METHODS: Effects of nifedipine and nicardipine on the high Kf-induced intracellular Ca2+ concentration ([Ca2+](i)) increase were studied by measuring [Ca2+](i) using the fluorescent indicator Fura-2. RESULTS: Pretreatment of cells with nifedipine 50 mu mol L-l inhibited the high K+-induced [Ca2+](i) transient by about 60 % (n = 3); however, pretreatment of cells with nicardipine 10 mu mol.L-1 completely prevented the high Kt-evoked [Ca2+](i) increase in dibutyryl cyclic AMP (dbcAMP)-differentiated NG 108-15 cells (n =5). The high K+-induced [Ca2+](i) increase was mediated by L and N-type voltage-sensitive calcium channels (VSCC) in NC 108-15 cells. CONCLUSION: Nicardipine at micromolar range inhibited both L- and N-type VSCC in dbcAMP-differentiated NG 108-15 cells whereas nifedipine mainly inhibited L-type calcium channels.
引用
收藏
页码:117 / 120
页数:4
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