Selected peptides targeted to the NMDA receptor channel protect neurons from excitotoxic death

被引:43
作者
Ferrer-Montiel, AV
Merino, JM
Blondelle, SE
Perez-Payà, E
Houghten, RA
Montal, M [1 ]
机构
[1] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
[2] Torrey Pines Inst Mol Studies, San Diego, CA 92121 USA
关键词
combinatorial chemistry; drug discovery; ion channel blockers; neuroprotection; glutamate receptor;
D O I
10.1038/nbt0398-286
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Excitotoxic neuronal death, associated with neurodegeneration and stroke, is triggered primarily by massive Ca2+ influx arising from overactivation of glutamate receptor channels of the N-methyl-D-aspartate (NMDA) subtype. To search for channel blockers, synthetic combinatorial libraries were assayed for block of agonist-evoked currents by the human NR1-NR2A NMDA receptor subunits expressed in amphibian oocytes. A set of arginine-rich hexapeptides selectively blocked the NMDA receptor channel with IC50 approximately 100 nM, a potency similar to clinically tolerated blockers such as memantine, and only marginally blocked on non-NMDA glutamate receptors. These peptides prevent neuronal cell death elicited by an excitotoxic insult on hippocampal cultures.
引用
收藏
页码:286 / 291
页数:6
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