THE SELECTIVE ADENOSINE-A2 RECEPTOR AGONIST CGS 21680 ENHANCES EXCITATORY TRANSMITTER AMINO-ACID RELEASE FROM THE ISCHEMIC RAT CEREBRAL-CORTEX

被引：102

作者：

OREGAN, MH ^{[1
]}

SIMPSON, RE ^{[1
]}

PERKINS, LM ^{[1
]}

PHILLIS, JW ^{[1
]}

机构：

[1] WAYNE STATE UNIV, SCH MED, DEPT PHYSIOL, 540 E CANFIELD, DETROIT, MI 48201 USA

来源：

NEUROSCIENCE LETTERS | 1992年 / 138卷 / 01期

关键词：

ISCHEMIA; ADENOSINE; ADENOSINE-A1; RECEPTOR; ADENOSINE-A2; EXCITOTOXIN;

D O I：

10.1016/0304-3940(92)90498-V

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

The effects of the selective adenosine A, receptor agonist 2-p-(2-carboxyethyl)phenethylamino-5'-N-ethylcarboxamido adenosine hydrochloride (CGS 21680) on aspartate and glutamate release from the ischemic rat cerebral cortex were studied with the cortical cup technique. Cerebral ischemia (20 min) was elicited by four vessel occlusion. Pretreatment with CGS 21680 failed to alter basal excitatory amino acid levels, however, CGS 21680 at 10(-6) M significantly enhanced the ischemia-evoked release. Thus, aspartate and glutamate release during ischemia can be stimulated via the activation of A, receptors, in addition to the suppression of excitatory amino acid release mediated by selective A, receptor agonists.

引用

页码：169 / 172

页数：4

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