THE SLOW INHIBITORY POSTSYNAPTIC POTENTIAL IN RAT HIPPOCAMPAL CA1 NEURONS IS BLOCKED BY INTRACELLULAR INJECTION OF QX-314

被引:169
作者
NATHAN, T [1 ]
JENSEN, MS [1 ]
LAMBERT, JDC [1 ]
机构
[1] AARHUS UNIV,INST PHYSIOL,PHARMABIOT RES CTR,DK-8000 AARHUS C,DENMARK
关键词
CA1 pyramidal cell; GABA[!sub]B[!/sub] receptor; Hippocampus; Inhibitory postsynaptic potential; Lidocaine derivative; QX-314;
D O I
10.1016/0304-3940(90)90865-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Intracellular recordings were made from CA1 pyramidal neurones in the rat hippocampus slice preparation. The recording electrodes contained potassium acetate (4 M) with or without the quaternary lidocaine derivative, QX-314 (50 mM). Both fast (f) and slow (s) inhibitory postsynaptic potentials (IPSP) were evoked by low-frequency orthodromic stimulation. The s-IPSP was rapidly reduced by QX-314 injection. It decreased along a similar time course to the dV/dt of the action potential (AP). The f-IPSP and excitatory postsynaptic potential were not significantly reduced in size at a time when the s-IPSP was virtually abolished by QX-314. It is concluded that conductance through the K+ channels which are coupled to GABAB receptors is readily blocked by QX-314, while the Cl- channels which are coupled to GABAA receptors and the cation channels coupled to the glutamate receptors are relatively resistant to the local anaesthetic. © 1990.
引用
收藏
页码:309 / 313
页数:5
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