EFFECTS OF THAPSIGARGIN, AN INTRACELLULAR CA2+ PUMP INHIBITOR, ON INSULIN RELEASE BY RAT PANCREATIC B-CELL

被引:11
作者
AIZAWA, T [1 ]
YADA, T [1 ]
ASANUMA, N [1 ]
SATO, Y [1 ]
ISHIHARA, F [1 ]
HAMAKAWA, N [1 ]
YAEKURA, K [1 ]
HASHIZUME, K [1 ]
机构
[1] KAGOSHIMA UNIV,SCH MED,DEPT PHYSIOL,KAGOSHIMA,JAPAN
关键词
THAPSIGARGIN; PANCREATIC B-CELL; INSULIN RELEASE; INTRACELLULAR CA2+;
D O I
10.1016/0024-3205(95)02095-Z
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This is the first report as to the effects of thapsigargin (Tg), an inhibitor of intracellular Ca2+ pumps, on insulin release by pancreatic B-cells. Tg does not alter basal insulin release by the isolated islets, with 3 mM glucose. However, it potentiates high glucose-induced insulin release: potentiation of the first phase response is dose-related in a concentration range of 1.3-40 mu M. In isolated B-cells, Tg causes a minimal rise in basal cytosolic free calcium concentration ([Ca2+](i)) and eliminates high glucose-induced initial lowering of [Ca2+](i). Tg does not alter glucose oxidation by the islets and the islet insulin content. An elimination of glucose-induced sequestration of Ca2+ into Tg-sensitive intracellular pool(s) is considered to be the cause of Tg potentiation of glucose effect on insulin release.
引用
收藏
页码:1375 / 1381
页数:7
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