PAF ACTIVATION OF A VOLTAGE-GATED R-TYPE CA(2+) CHANNEL IN HUMAN AND CANINE AORTIC ENDOTHELIAL-CELLS

被引:43
作者
BKAILY, G
DORLEANSJUSTE, P
NAIK, R
PERODIN, J
STANKOVA, J
ABDULNOUR, E
ROLAPLESZCZYNSKI, M
机构
[1] UNIV SHERBROOKE,FAC MED,DEPT IMMUNOL,SHERBROOKE J1H 5N4,QUEBEC,CANADA
[2] UNIV SHERBROOKE,FAC MED,DEPT PHARMACOL,SHERBROOKE J1H 5N4,QUEBEC,CANADA
[3] UNIV SHERBROOKE,FAC MED,DEPT SURG,SHERBROOKE J1H 5N4,QUEBEC,CANADA
关键词
ENDOTHELIAL CELLS; CA(2+) CHANNEL; PAF; CALCIUM BLOCKERS; CALCIUM;
D O I
10.1111/j.1476-5381.1993.tb13841.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
By the use of fura-2 and digital imaging techniques, [K]o depolarization or PAF (10(-9)M) were shown to induce a sustained increase of [Ca]i in human or canine single aortic vascular endothelial cells (VEC) that was insensitive to nifedipine but sensitive to (-)-PN200-110 or to lowering of [Ca]o. The PAF-induced effect on [Ca]i was blocked by the PAF receptor antagonist, WEB2170. Our results suggest that [K]o depolarization and PAF increase [Ca]i via the activation of R-type Ca2+ channels.
引用
收藏
页码:519 / 520
页数:2
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