摘要
INTRODUCTIONDihydropyridineshavelongbeenconsideredtobeagroupofinhibitorsofLtypevoltagesensitiveCa2+channels(VSCC).Recently,...
AIM: To investigate the possibility of dihydropyridine inhibition of N type calcium channels. METHODS: Effects of nifedipine and nicardipine on the high K + induced intracellular Ca 2+ concentration ([Ca 2+ ] i) increase were studied by measuring [Ca 2+ ] i using the fluorescent indi ̄cat ̄or Fura 2. RESULTS: Pretreatment of cells with nifedipine 50 μmol·L -1 inhibited the high K + induc ̄ed [Ca 2+ ] i transient by about 60 % ( n =3); however, pretreatment of cells with nicardipine 10 μmol·L -1 completely prevented the high K + evoked [Ca 2+ ] i increase in dibutyryl cyclic AMP (dbcAMP) differentiated NG 108 15 cells ( n =5). The high K + induced [Ca 2+ ] i increase was mediated by L and N type voltage sensitive calcium channels (VSCC) in NG 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.
出处
《中国药理学报》
CSCD
1999年第2期117-120,共4页
Acta Pharmacologica Sinica
关键词
二氢吡啶
尼卡地平
DBCAMP
神经母细胞瘤
dihydropyridines
nicardipine
nifedipine
calcium channels
Fura 2
cyclic AMP
NG 108 15 cells