Rössler Anne-Sophie, Rüthrich Heinz, Krug Manfred, Dodd Robert H, Chapouthier Georges, Grecksch Gisela
UMR 7593 CNRS, Medical Faculty Pitié-Salpêtrière, 75013 Paris, France.
Exp Brain Res. 2002 Sep;146(1):77-85. doi: 10.1007/s00221-002-1159-9. Epub 2002 Jul 16.
The present work analyzed the changes in evoked field potentials of freely moving rats after kindling induced by a convulsant inverse agonist of the GABA(A)-benzodiazepine receptor complex, methyl beta-carboline-3-carboxylate (beta-CCM). Two doses of beta-CCM (2 mg/kg and 4 mg/kg) were used. In kindled and control animals, a stimulating electrode was implanted in the perforant pathway and a recording electrode in the dentate gyrus. Results showed that, after an acutely injected dose of 20 mg/kg pentylenetetrazol (PTZ), all kindled animals showed a decrease in population spike amplitude after 20 min. After 60 min, only fully kindled rats showed a long-lasting potentiation, also visible up to 24 h later, as compared to controls or nonkindled animals. Changes in glutamate and GABA receptor binding measured in previous experiments may explain this potentiation effect observed in fully kindled rats.
本研究分析了由GABA(A)-苯二氮䓬受体复合物的惊厥性反向激动剂β-咔啉-3-羧酸甲酯(β-CCM)诱发点燃后自由活动大鼠诱发电位场的变化。使用了两种剂量的β-CCM(2mg/kg和4mg/kg)。在点燃和对照动物中,将刺激电极植入穿通通路,将记录电极植入齿状回。结果显示,急性注射20mg/kg戊四氮(PTZ)后,所有点燃动物在20分钟后群体峰电位幅度降低。60分钟后,与对照或未点燃动物相比,只有完全点燃的大鼠出现持久增强,这种增强在24小时后仍可见。先前实验中测得的谷氨酸和GABA受体结合变化可能解释了在完全点燃大鼠中观察到的这种增强效应。