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PMID: 2446331 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Modulation of sodium-channel mRNA levels in rat skeletal muscle.

Cooperman SS, Grubman SA, Barchi RL, Goodman RH, Mandel G

Abstract

Action potentials in many types of excitable cells result from changes in permeability to Na ions. Although these permeability changes in nerve and muscle are mediated by voltage-gated Na channels that are functionally similar, we found that the Na-channel gene expressed in skeletal muscle is different from the genes coding for two Na channels (type I and type II) in brain. Despite the structural differences between muscle and brain Na-channel genes, a cDNA clone derived from rat brain hybridizes to skeletal muscle Na-channel mRNA of approximately 9.5 kilobases. We used this cDNA probe to measure changes in Na-channel mRNA levels in skeletal muscle during development and following denervation. By blot hybridization analysis of electrophoretically fractionated RNA, we found that Na-channel mRNA can be detected as early as embryonic day 17 and that mRNA levels increase 2-fold between birth and postnatal day 35. Denervation of adult muscle causes a further 2- to 3-fold increase in muscle Na-channel mRNA levels, suggesting that expression of Na-channel genes in fast-twitch muscle may be regulated by the state of innervation.

MeSH Terms
Age Factors Animals Gene Expression Regulation Ion Channels/physiology Muscle Denervation Muscle Development Muscles/physiology Nucleic Acid Hybridization RNA, Messenger/genetics Rats Sodium/physiology
Chemicals
Ion Channels RNA, Messenger Sodium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cooperman S S
Department of Medicine, Tufts-New England Medical Center, Boston, MA 02111.
Grubman S A
Barchi R L
Goodman R H
Mandel G
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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
1987-12-00
Pages
8721-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC299618
Subset
IM
Grants
NINDS NIH HHS · NS22518 · United States
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