Seizure suppression by adenosine A2A receptor activation in a rat model of audiogenic brainstem epilepsy

被引:55
作者
Huber, A
Güttinger, M
Möhler, H
Boison, D
机构
[1] Swiss Fed Inst Technol, Dept Appl Biosci, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Inst Pharmacol & Toxicol, CH-8057 Zurich, Switzerland
关键词
epilepsy; adenosine; A(2A) receptor; A(1) receptor; audiogenic seizures;
D O I
10.1016/S0304-3940(02)00684-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adenosine is known to suppress seizure activity mainly by activation of adenosine A(1) receptors. However, little is known about the potential involvement of other types of adenosine receptors in seizure suppression. It was now tested whether activation of adenosine A(2A) receptors would be effective in the suppression of generalized brainstem seizures. Genetically epilepsy-prone rats were intraperitoneally injected with increasing doses of the A(2A) receptor agonist, 5'-(N-cyclopropyl)carboxamido-adenosine (CPCA), and, for comparison, with the A, receptor agonist, 2-chloro-N-6-cyclopentyladenosine (CCPA). Both CPCA and CCPA were effective in suppressing generalized brainstem seizures with minimal effective concentrations of 2.5 and 1.5 mg/kg, respectively. Seizure suppression was maintained when CPCA was co-injected with the peripherally acting adenosine receptor antagonist 8-(p-sulphophenyl)theophylline, suggesting that central activation of A(2A) receptors effectively contributes to seizure suppression. (C) 2002 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:289 / 292
页数:4
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