NMDA AND QUISQUALATE REDUCE A CA-DEPENDENT K+ CURRENT BY A PROTEIN KINASE-MEDIATED MECHANISM

被引:75
作者
BASKYS, A
BERNSTEIN, NK
BAROLET, AW
CARLEN, PL
机构
[1] ADDICT RES FDN,TORONTO M5S 2S1,ONTARIO,CANADA
[2] UNIV TORONTO,DEPT PHYSIOL,TORONTO M5S 1A1,ONTARIO,CANADA
[3] UNIV TORONTO,DIV LIFE SCI,SCARBOROUGH,ONTARIO,CANADA
关键词
Calcium-dependent potassium current; Dentate granule neuron; N-Methyl-d-aspartate; Protein kinase inhibitor; Quisqualate; α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid;
D O I
10.1016/0304-3940(90)90325-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stimulation of N-methyl-d-aspartate (NMDA) or quisqualate (Quis) receptors by submicromolar concentrations of NMDA or Quis but not α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) reduced post-spike train afterhyperpolarizations (AHPs) and blocked the underlying Iaph in dentate granule (DG) neurones in vitro. The NMDA but not Quis action was blocked by the NMDA receptor blocker 2-d,l-aminophosphonovaleric acid (APV). Actions of both NMDA and Quis were abolished by isoquino-linesulphonyl-2-methyl-piperazine dihydrochloride (H-7), an inhibitor of several protein kinases. These data suggest that there is a link between excitatory amino acid receptor activation, the protein kinase system, and neuronal excitability. © 1990.
引用
收藏
页码:76 / 81
页数:6
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