Perampanel Inhibition of AMPA Receptor Currents in Cultured Hippocampal Neurons

被引:117
作者
Chen, Chao-Yin [1 ]
Matt, Lucas [1 ]
Hell, Johannes Wilhelm [1 ]
Rogawski, Michael A. [2 ,3 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Pharmacol, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Med, Dept Neurol, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Ctr Neurosci, Sacramento, CA 95817 USA
基金
美国国家卫生研究院;
关键词
GLUTAMATE-RECEPTOR; ANTAGONISM; 2,3-DIHYDROXY-6-NITRO-7-SULFAMOYL-BENZO(F)QUINOXALINE; 2,3-BENZODIAZEPINE; CYCLOTHIAZIDE; RESPONSES;
D O I
10.1371/journal.pone.0108021
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Perampanel is an aryl substituted 2-pyridone AMPA receptor antagonist that was recently approved as a treatment for epilepsy. The drug potently inhibits AMPA receptor responses but the mode of block has not been characterized. Here the action of perampanel on AMPA receptors was investigated by whole-cell voltage-clamp recording in cultured rat hippocampal neurons. Perampanel caused a slow (tau similar to 1 s at 3 mu M), concentration-dependent inhibition of AMPA receptor currents evoked by AMPA and kainate. The rates of block and unblock of AMPA receptor currents were 1.5 x 10(5) M-1 s(-1) and 0.58 s(-1), respectively. Perampanel did not affect NMDA receptor currents. The extent of block of non-desensitizing kainate-evoked currents (IC50, 0.56 mu M) was similar at all kainate concentrations (3-100 mu M), demonstrating a noncompetitive blocking action. Parampanel did not alter the trajectory of AMPA evoked currents indicating that it does not influence AMPA receptor desensitization. Perampanel is a selective negative allosteric AMPA receptor antagonist of high-affinity and slow blocking kinetics.
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页数:7
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