Lu C H, Lee K C, Chen Y C, Cheng J S, Yu M S, Chen W C, Jan C R
Department of Neurology, Chang Gung Memorial Hospital-Kaohsiung, Kaohsiung Veterans General Hospital, Taiwan.
Pharmacol Toxicol. 2000 Oct;87(4):149-55. doi: 10.1034/j.1600-0773.2000.d01-65.x.
The effect of lindane (gamma-hexachlorocyclohexane), an organochlorine pesticide, on Ca2+ mobilization in Madin-Darby canine kidney cells was examined by fluorimetry using fura-2 as a Ca2+ indicator. Lindane (5-200 microM) increased [Ca2+]i concentration-dependently. The [Ca2+]i signal comprised an immediate initial rise followed by a persistent phase. Ca2+ removal inhibited the [Ca2+]i signal by reducing both the initial rise and the sustained phase. This implies lindane-triggered Ca2+ influx and Ca2+ release. In Ca2+ -free medium, 0.15 mM lindane increased [Ca2+]i after pretreatment with carbonylcyanide m-chlorophenylhydrazone (CCCP, 2 microM), a mitochondrial uncoupler, and two endoplasmic reticulum Ca2+ pump inhibitors, thapsigargin and cyclopiazonic acid. Conversely, pretreatment with lindane abolished CCCP- and thapsigargin-induced Ca2+ release. This suggests that 0.15 mM lindane released Ca2+ from the endoplasmic reticulum, mitochondria and other stores. La3+ (1 mM) partly inhibited 0.1 mM lindane-induced [Ca2+]i increase, confirming that lindane induced Ca2+ influx. Addition of 3 mM Ca2+ increased [Ca2+]i after pretreatment with 0.15 mM lindane for 750 sec. in Ca2+ -free medium, which indicates lindane-induced capacitative Ca2+ entry. Lindane (0.15 mM)-induced Ca2+ release was not reduced by inhibiting phospholipase C with 2 microM U73122, but was inhibited by 70% by the phospholipase A2 inhibitor aristolochic acid (40 microM).
采用荧光法,以fura-2作为Ca2+指示剂,研究了有机氯农药林丹(γ-六氯环己烷)对Madin-Darby犬肾细胞中Ca2+动员的影响。林丹(5 - 200微摩尔)浓度依赖性地增加了[Ca2+]i浓度。[Ca2+]i信号包括一个立即出现的初始上升阶段,随后是一个持续阶段。Ca2+的去除通过减少初始上升阶段和持续阶段来抑制[Ca2+]i信号。这意味着林丹引发了Ca2+内流和Ca2+释放。在无Ca2+培养基中,0.15毫摩尔林丹在用羰基氰化物间氯苯腙(CCCP,2微摩尔)预处理后增加了[Ca2+]i,CCCP是一种线粒体解偶联剂,还有两种内质网Ca2+泵抑制剂,毒胡萝卜素和环匹阿尼酸。相反,用林丹预处理可消除CCCP和毒胡萝卜素诱导的Ca2+释放。这表明0.15毫摩尔林丹从内质网、线粒体和其他储存部位释放了Ca2+。1毫摩尔La3+部分抑制了0.1毫摩尔林丹诱导的[Ca2+]i增加,证实了林丹诱导了Ca2+内流。在无Ca2+培养基中,用0.15毫摩尔林丹预处理750秒后,加入3毫摩尔Ca2+增加了[Ca2+]i,这表明林丹诱导了容量性Ca2+内流。用2微摩尔U73122抑制磷脂酶C并不能减少林丹(0.15毫摩尔)诱导的Ca2+释放,但磷脂酶A2抑制剂马兜铃酸(40微摩尔)可使其减少70%。