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PMID: 1670922 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Postsynaptic factors control the duration of synaptic enhancement in area CA1 of the hippocampus.

Neuron ·Vol. 6 ·No. 1 ·1991-01-00 ·Pages 53-60

Malenka RC

Abstract

In area of CA1 of the hippocampus, at least two phases of long-term potentiation (LTP) can be isolated: an early decremental component referred to as short-term potentiation (STP), which precedes a long-lasting, nondecremental component commonly considered to be stable LTP. Utilizing the hippocampal slice preparation, experiments were performed to determine the physiological factors controlling the conversion of STP to LTP. The duration of NMDA receptor-dependent synaptic enhancement was influenced by several factors, including the degree of postsynaptic NMDA receptor activation and the magnitude and timing of postsynaptic membrane depolarization during synaptic transmission. It was possible to convert STP to LTP by manipulations that increased the influx of calcium into the postsynaptic cell. These results demonstrate that NMDA receptor activation can result in distinct forms of synaptic potentiation and imply that the magnitude of postsynaptic calcium increase is a critical variable controlling the duration of synaptic enhancement.

MeSH Terms
2-Amino-5-phosphonovalerate/pharmacology Animals Calcium/physiology Electric Stimulation Electrophysiology Hippocampus/physiology Kinetics N-Methylaspartate/pharmacology Neurotransmitter Agents/pharmacology Rats Receptors, N-Methyl-D-Aspartate/drug effects,physiology Second Messenger Systems Synapses/drug effects,physiology
Chemicals
Neurotransmitter Agents Receptors, N-Methyl-D-Aspartate N-Methylaspartate 2-Amino-5-phosphonovalerate Calcium
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Malenka R C
Department of Psychiatry, University of California, San Francisco 94143.
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1991-01-00
Pages
53-60
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NIMH NIH HHS · MH45334 · United States
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