Loperamide: novel effects on capacitative calcium influx

被引:21
作者
Daly, JW [1 ]
Harper, J [1 ]
机构
[1] Natl Inst Hlth, Bioorgan Chem Lab, Bethesda, MD 20892 USA
关键词
loperamide; calcium channels; calcium stores; maitotoxin; inositol trisphosphate; thapsigargin; ATP;
D O I
10.1007/s000180050504
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Loperamide is a widely used antidiarrheal that primarily acts at nanomolar concentrations through activation of opioid receptors in the gastrointestinal tract. At somewhat higher concentrations, loperamide blocks calmodulin activity, calcium channels, N-methyl-D-aspartate-receptor channels, and maitotoxin-elicited calcium influx. Loperamide at micromolar concentrations has now been shown to have a remarkable stimulatory effect on the capacitative calcium influx that is triggered in many cells by depletion of the inositol-trisphosphate-sensitive stores of calcium in the endoplasmic reticulum. The mechanism whereby loperamide enhances levels of intracellular calcium elevated by capacitative calcium influx is, as yet, undefined.
引用
收藏
页码:149 / 157
页数:9
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