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PMID: 6310084 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effects of excitatory amino acids and their antagonists on membrane and action potentials of cat caudate neurones.

The Journal of physiology ·Vol. 339 ·1983-06-00 ·Pages 207-22

Herrling PL, Morris R, Salt TE

Abstract

The electrical activity of caudate neurones was recorded with intracellular electrodes in halothane anaesthetized cats. Agonists and antagonists of excitatory amino acid receptors were applied by micro-ionophoresis and their effects on membrane- and action potentials and on cortically evoked synaptic potentials evaluated. The agonists, L-aspartate (asp), L-glutamate (glu), N-methyl-DL-aspartate (NMA), quinolinate and quisqualate all depolarized the membrane, caused repetitive firing, reduced the apparent amplitude of the cortically evoked excitatory post-synaptic potentials (e.p.s.p.s) and increased the amplitude of the associated inhibitory post-synaptic potential. Two of the agonists, NMA and quinolinate, additionally caused the appearance of up to 500 ms long depolarizations (plateaus) on the falling phase of action potentials. These plateaus were seen in about two-thirds of the cells in this sample while in the other third the excitatory effects of NMA and quinolinate were indistinguishable from those of glu and quisqualate. The N-methyl-D-aspartate (NMDA) receptor antagonist D-alpha-aminoadipate (DAA) reversibly inhibited the effects of NMA and quinolinate but only on those cells where these two agents evoked action potential plateaus while on the same cells the effects of asp, glu and quisqualate were either only weakly antagonized or not affected. On cells not displaying plateaus to NMA or quinolinate none of the effects of the agonists could be antagonized by DAA. DAA applications that completely antagonized the effects of NMA never reduced the amplitudes of cortically evoked e.p.s.p.s. Cis-2,3-piperidine dicarboxylate also blocked the effects of NMA and asp at low application currents while at higher currents it enhanced the effects of glu or asp although still retaining its NMA antagonistic activity. High-frequency stimulation of the cortico-caudate pathway resulted in long-lasting depolarizations and repetitive firing, but plateaus of the type caused by NMA or quinolinate were not seen.

MeSH Terms
2-Aminoadipic Acid/pharmacology Action Potentials/drug effects Amino Acids/pharmacology Animals Aspartic Acid/analogs & derivatives,antagonists & inhibitors,pharmacology Cats Caudate Nucleus/physiology Female Glutamates/pharmacology Male Membrane Potentials/drug effects N-Methylaspartate Oxadiazoles/pharmacology Pipecolic Acids/pharmacology Quinolinic Acid Quinolinic Acids/pharmacology Quisqualic Acid Receptors, Cell Surface/drug effects Receptors, N-Methyl-D-Aspartate
Chemicals
Amino Acids Glutamates Oxadiazoles Pipecolic Acids Quinolinic Acids Receptors, Cell Surface Receptors, N-Methyl-D-Aspartate 2-Aminoadipic Acid Aspartic Acid 2,3-piperidinedicarboxylic acid N-Methylaspartate Quisqualic Acid Quinolinic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Herrling P L
Morris R
Salt T E
References (39)
39 references, click to expand
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Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1983-06-00
Pages
207-22
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1199157
Subset
IM
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