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PMID: 9356419 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

A fast synaptic potential mediated by NMDA and non-NMDA receptors.

Journal of neurophysiology ·Vol. 78 ·No. 5 ·1997-11-00 ·Pages 2693-706

Wolszon LR, Pereda AE, Faber DS

Abstract

A fast synaptic potential mediated by NMDA and non-NMDA receptors. J. Neurophysiol. 78: 2693-2706, 1997. Excitatory synaptic transmission in the CNS often is mediated by two kinetically distinct glutamate receptor subtypes that frequently are colocalized, the N-methyl--aspartate (NMDA) and non-NMDA receptors. Their synaptic currents are typically very slow and very fast, respectively. We examined the pharmacological and physiological properties of chemical excitatory transmission at the mixed electrical and chemical synapses between auditory afferents and the goldfish Mauthner cell, in vivo. Previous physiological data have suggested the involvement of glutamate receptors in this fast excitatory postsynaptic potential (EPSP), the chemical component of which decays with a time constant of <2 ms. We demonstrate here that the pharmacological and voltage-dependent characteristics of the synaptic currents are consistent with glutamatergic transmission and that both NMDA and non-NMDA receptors are involved. The two components surprisingly exhibit quite similar kinetics even at resting potential, with the NMDA response being only slightly slower. Due to its fast kinetics and characteristic voltage dependence, NMDA receptor-mediated transmission at these first-order synapses contributes significantly to paired pulse and frequency-dependent facilitation of successive fast EPSPs during high-frequency repetitive firing, a presynaptic impulse pattern that induces activity-dependent homosynaptic changes in both electrical and chemical transmission. Thus NMDA receptor kinetics in this intact preparation are suited to its functional requirements, namely speed of information transmission and the ability to trigger changes in synaptic efficacy.

MeSH Terms
2-Amino-5-phosphonovalerate/pharmacology 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology Animals Electric Stimulation/instrumentation,methods Excitatory Amino Acid Antagonists/pharmacology Excitatory Postsynaptic Potentials/drug effects,physiology Goldfish Kainic Acid/pharmacology Ketamine/pharmacology Microelectrodes Neurons/cytology,drug effects,physiology Piperazines/pharmacology Pons/cytology,physiology Receptors, Glutamate/drug effects,physiology Receptors, N-Methyl-D-Aspartate/drug effects,physiology Serotonin Antagonists/pharmacology Synapses/drug effects,physiology Synaptic Transmission/drug effects,physiology
Chemicals
Excitatory Amino Acid Antagonists Piperazines Receptors, Glutamate Receptors, N-Methyl-D-Aspartate Serotonin Antagonists Ketamine 6-Cyano-7-nitroquinoxaline-2,3-dione 2-Amino-5-phosphonovalerate 1-(3-chlorophenyl)piperazine Kainic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wolszon L R
Department of Neurobiology and Anatomy, MCP Hahnemann School of Medicine, Allegheny University of the Health Sciences, Philadelphia, Pennsylvania 19129, USA.
Pereda A E
Faber D S
Article Info
Journal
Journal of neurophysiology
Abbr.
J Neurophysiol
ISSN
0022-3077
Published
1997-11-00
Pages
2693-706
Language
English
Region
United States
NLM ID
0375404
Subset
IM
Grants
NINDS NIH HHS · NS-21848 · United States
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