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PMID: 9159170 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Long-term potentiation involves increases in the probability of neurotransmitter release.

Schulz PE

Abstract

There is great interest in understanding the mechanisms of expression underlying long-term potentiation (LTP). They are agreed to involve an increase in synaptic efficacy, which is described by three multiplicative parameters: p, the probability of neurotransmitter release; n, the number of active release sites; and q, the postsynaptic unit response to transmitter release. We report three new lines of evidence suggesting that increases in p contribute to LTP expression. (i) When the contributions to LTP by p, n, and q are maximized, and p alone is decreased, another high-frequency stimulation elicits additional LTP. The additional potentiation is only associated with decreases in paired-pulse facilitation (PPF) suggesting an increase in p. (ii) There is an inverse relationship between baseline p [corrected] and the magnitude of LTP elicited, consistent with p [corrected] having more or less room to increase when p is smaller or greater. (iii) It has been shown that there is an inverse relationship between the magnitude of LTP induced and the associated changes in PPF. Now I find that decreasing p before inducing LTP moves the set-point for measuring those changes in PPF from before to after p is decreased, which would only occur if p contributes to LTP. Three lines of evidence, then, suggest that increases in p contribute to LTP expression, which is consistent with a presynaptic contribution to LTP. These experiments do not address potential postsynaptic contributions.

MeSH Terms
2-Amino-5-phosphonovalerate/pharmacology 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology Animals Baclofen/analogs & derivatives,pharmacology Cadmium Chloride/pharmacology Calcium Channel Blockers/pharmacology Evoked Potentials/drug effects Hippocampus/drug effects,physiology In Vitro Techniques Long-Term Potentiation/drug effects,physiology Neurotransmitter Agents/metabolism Peptides/pharmacology Probability Rats Rats, Sprague-Dawley Receptors, AMPA/physiology Receptors, GABA-B/physiology Receptors, N-Methyl-D-Aspartate/physiology Synapses/physiology Synaptic Transmission/drug effects Time Factors omega-Conotoxin GVIA
Chemicals
Calcium Channel Blockers Neurotransmitter Agents Peptides Receptors, AMPA Receptors, GABA-B Receptors, N-Methyl-D-Aspartate 6-Cyano-7-nitroquinoxaline-2,3-dione 2-Amino-5-phosphonovalerate omega-Conotoxin GVIA Baclofen Cadmium Chloride 2-hydroxysaclofen
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schulz P E
Department of Neurology and Division of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA. pschulz@bcm.tmc.edu
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1997-05-27
Pages
5888-93
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC20876
Subset
IM
Corrections
ErratumIn
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