Johnson J D, Conroy W G, Isom G E
Toxicol Appl Pharmacol. 1987 Apr;88(2):217-24. doi: 10.1016/0041-008x(87)90007-x.
The effect of KCN on cytosolic Ca2+ levels was measured in PC12 cells using Quin II/AM, a fluorometric calcium indicator. The resting cytosolic Ca2+ concentration, 115.0 +/- 4.9 nm, increased gradually and steadily over a 30-min time period following addition of 10(-4), 10(-3), or 10(-2)M KCN to the cells. After 15 min, 10(-3) and 10(-2)M KCN produced a three- and sixfold increase in the cytosolic Ca2+ concentration, respectively. In K+-depolarized cells, KCN induced a more rapid rise of intracellular calcium than in cells treated with KCN or KCI alone. KCN and/or K+-induced accumulation of cytosolic Ca2+ was blocked when the cells were pretreated with 10(-5)M diltiazem (a calcium channel blocker). These results demonstrate in a cell model that cyanide induces an accumulation of cytosolic Ca2+ and this additional cytosolic Ca2+ load appears to originate primarily from the extracellular compartment. This study supports previous reports implicating calcium as an intracellular mediator of cyanide toxicity.
使用荧光钙指示剂喹哪啶红/AM(Quin II/AM)在PC12细胞中测量了氰化钾(KCN)对胞质Ca2+水平的影响。在向细胞中添加10^(-4)、10^(-3)或10^(-2)M KCN后的30分钟时间段内,静息胞质Ca2+浓度(115.0±4.9 nM)逐渐稳定升高。15分钟后,10^(-3)和10^(-2)M KCN分别使胞质Ca2+浓度增加了三倍和六倍。在K+去极化的细胞中,KCN诱导的细胞内钙升高比单独用KCN或KCl处理的细胞更快。当细胞用10^(-5)M地尔硫䓬(一种钙通道阻滞剂)预处理时,KCN和/或K+诱导的胞质Ca2+积累被阻断。这些结果在细胞模型中表明,氰化物会诱导胞质Ca2+积累,并且这种额外的胞质Ca2+负荷似乎主要源于细胞外区室。本研究支持了先前有关钙作为氰化物毒性细胞内介质的报道。