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PMID: 1720572 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A requirement for the intercellular messenger nitric oxide in long-term potentiation.

Science (New York, N.Y.) ·Vol. 254 ·No. 5037 ·1991-12-06 ·Pages 1503-6

Schuman EM, Madison DV

Abstract

Long-term potentiation (LTP) of synaptic transmission is a widely studied model of neuronal plasticity. The induction of LTP is known to require processes in the postsynaptic neuron, while experimental evidence suggests that the expression of LTP may occur in the presynaptic terminal. This has led to speculation that a retrograde messenger travels from the post- to the presynaptic cell during induction of LTP. Extracellular application or postsynaptic injection of two inhibitors of nitric oxide synthase, N-nitro-L-arginine or NG-methyl-L-arginine, blocks LTP. Extracellular application of hemoglobin, which binds nitric oxide, also attenuates LTP. These findings suggest that nitric oxide liberated from postsynaptic neurons may travel back to presynaptic terminals to cause LTP expression.

MeSH Terms
Amino Acid Oxidoreductases/antagonists & inhibitors Arginine/analogs & derivatives,pharmacology Hippocampus/physiology In Vitro Techniques Neuronal Plasticity Nitric Oxide/metabolism Nitric Oxide Synthase Nitroarginine Synaptic Membranes/physiology Synaptic Transmission omega-N-Methylarginine
Chemicals
Nitroarginine omega-N-Methylarginine Nitric Oxide Arginine Nitric Oxide Synthase Amino Acid Oxidoreductases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Schuman E M
Department of Molecular and Cellular Physiology, Beckman Center for Molecular and Genetic Medicine, Stanford University School of Medicine, CA 94305-5426.
Madison D V
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1991-12-06
Pages
1503-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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