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PMID: 6328531 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Spontaneous openings of the acetylcholine receptor channel.

Jackson MB

Abstract

Patch clamp recordings from embryonic mouse muscle cells in culture revealed spontaneous openings of the acetylcholine receptor channel in the absence of exogenously applied cholinergic agent. The conductance of the spontaneous channel currents was, within experimental error, identical with the conductance of suberyldicholine-activated channel currents. The comparison of channel conductance was made with sodium and with cesium, each at two concentrations, with the same result. Treatment of the cells with alpha-bungarotoxin blocked the spontaneous channel currents. To determine whether the spontaneous openings were caused by an endogenous agent with cholinergic activity a reactive disulfide bond near the receptor binding site was reduced with dithiothreitol and alkylated with N-ethylmaleimide. This chemical modification reduced the effectiveness with which suberyldicholine and curare activated channel currents but did not reduce the frequency of spontaneous openings. These experiments indicate that the acetylcholine receptor briefly and infrequently fluctuates into an active state in the absence of agonist. Agonist activation of the receptor presumably accelerates this spontaneously occurring process.

MeSH Terms
Animals Cell Membrane Permeability Ion Channels/physiology Kinetics Membrane Potentials Mice Neuromuscular Junction/physiology Receptors, Nicotinic/physiology
Chemicals
Ion Channels Receptors, Nicotinic
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Jackson M B
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24 references, click to expand
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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
1984-06-00
Pages
3901-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC345330
Subset
IM
Grants
NINDS NIH HHS · NS 19320-01 · United States
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