Sensitivity and density of glutamate receptor subtypes in the hippocampal formation are altered in pentylenetetrazole-kindled rats

被引:37
作者
Schroeder, H [1 ]
Becker, A [1 ]
Hoellt, V [1 ]
机构
[1] Otto Von Guericke Univ, Fac Med, Inst Pharmacol & Toxicol, D-39120 Magdeburg, Germany
关键词
chemical kindling; glutamate binding sites; NMDA; mGluR; inositol triphosphate;
D O I
10.1007/s002210050427
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Kindling induced by 13 intraperitoneal injections of 40 mg/kg pentylenetetrazole (PTZ) over a period of 4 weeks resulted in a significant long-lasting increase in both the convulsive susceptibility of animals to the convulsant and the density of the specific [H-3]-L-glutamate binding sites in the hippocampus. The quisqualate and kainate-sensitive [H-3]-L-glutamate binding sites were increased 24 h after the final PTZ injection, whereas the N-methyl-D-aspartate (NMDA)-sensitive sites had only a tendency to be enhanced. Furthermore, we investigated [3H]-L-glutamate binding on metabotropic receptors and found a significant increase in the hippocampus following PTZ kindling. In addition, in hippocampal tissue of kindled rats (+/-)-1-aminocyclopentane-trans-1,3-dicarboxylic acid (trans-ACPD)-stimulated inositol phosphate formation is increased. It can be concluded that the increase in metabotropic glutamate receptor (mGluR) density may be the expression of a specific enhancement in susceptibility of the glutamatergic systems to this excitatory amino acid developing in the course of PTZ-induced kindling.
引用
收藏
页码:527 / 530
页数:4
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