Ca2+ signalling and pancreatitis:: effects of alcohol, bile and coffee

被引:123
作者
Petersen, OH [1 ]
Sutton, R
机构
[1] Univ Liverpool, Physiol Lab, MRC Grp, Liverpool L69 3BX, Merseyside, England
[2] Univ Liverpool, Div Surg & Oncol, Liverpool L69 3BX, Merseyside, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.tips.2005.12.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ca2+ is a universal intracellular messenger that controls a wide range of cellular processes. In pancreatic acinar cells, acetylcholine and cholecystokinin regulate secretion via generation of repetitive local cytosolic Ca2+ signals in the apical pole. Bile acids and non-oxidative alcohol metabolites can elicit abnormal cytosolic Ca2+ signals that are global and sustained and result in necrosis. Necrosis results from excessive loss of Ca2+ from the endoplasmic reticulum, which is mediated by Ca2+ release through specific channels and inhibition of Ca2+ pumps in intracellular stores, followed by entry of extracellular Ca2+. Reduction of the cellular ATP level has a major role in this process. These abnormal Ca2+ signals, which can be inhibited by caffeine, explain how excessive alcohol intake and biliary disease cause acute pancreatitis, an often-fatal human disease in which the pancreas digests itself and its surroundings.
引用
收藏
页码:113 / 120
页数:8
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