Rat astroglial P2Z (P2X(7)) receptors regulate intracellular calcium and purine release

被引:128
作者
Ballerini, P
Rathbone, MP
DiIorio, P
Renzetti, A
Giuliani, P
DAlimonte, I
Trubiani, O
Caciagli, F
Ciccarelli, R
机构
[1] MCMASTER UNIV,HLTH SCI CTR,DEPT BIOMED SCI,HAMILTON,ON L8N 3Z5,CANADA
[2] MCMASTER UNIV,HLTH SCI CTR,DEPT MED,HAMILTON,ON L8N 3Z5,CANADA
[3] UNIV CHIETI,INST PHARMACOL & BIOMED TECHNOL,CHIETI,ITALY
[4] UNIV CHIETI,INST HUMAN MORPHOL,CHIETI,ITALY
关键词
primary astroglial cultures; extracellular purines; purinoceptors; P2X(7) (P2Z) subtype; membrane permeabilization; Ca2+](i) levels; H-3]purine release;
D O I
10.1097/00001756-199611040-00026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
TREATMENT Of rat astrocyte cultures with 2'- and 3'-O-(4-benzoylbenzoyl)-adenosine 5'-triphosphate (BzATP), a P2X(7) agonist, but not with adenosine 5-[alpha beta methylene] triphosphate (alpha,beta meATP), a P2X agonist, increased influx of extracellular Ca2+ and [Ca2+](i). Lucifer yellow, a small molecule which permeates P2X(7) receptor-induced pores, entered BzATP-treated but not control astrocytes. BzATP also stimulated efflux of [H-3]purine from cultured astrocytes. The P2X(7) receptor antagonist oxidized ATP abolished the effects of BzATP on [Ca2+](i) lucifer yellow permeation and [H-3]purine release, indicating that these effects were due to P2X(7) receptor activation. In neurological diseases or injuries extracellular ATP may activate P2X(7) receptors further enhancing [H-3]purine release, with important pathophysiological consequences.
引用
收藏
页码:2533 / 2537
页数:5
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