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PMID: 6146926 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The interaction of sea anemone and scorpion neurotoxins with tetrodotoxin-resistant Na+ channels in rat myoblasts. A comparison with Na+ channels in other excitable and non-excitable cells.

Molecular pharmacology ·Vol. 26 ·No. 1 ·1984-07-00 ·Pages 70-4

Frelin C, Vigne P, Schweitz H, Lazdunski M

Abstract

The properties of interactions of several polypeptide neurotoxins isolated from sea anemone and scorpion venom with Na+ channels of rat myoblasts, chick myotubes, neuroblastoma cells, and fibroblasts have been compared. Tetrodotoxin (TTX)-resistant Na+ channels appear to be much more sensitive to the action of sea anemone toxins than TTX-sensitive Na+ channels but have the same affinity for scorpion neurotoxins. This conclusion holds both for Na+ channels that can be activated electrically and for silent forms of Na+ channels. The sensitivity to sea anemone toxins of the different types of Na+ channels that have been studied suggests the existence of multiple forms of Na+ channels.

MeSH Terms
Animals Animals, Newborn Cells, Cultured Cnidarian Venoms/toxicity Drug Interactions Drug Resistance Ion Channels/drug effects,physiology Kinetics Muscles/physiology Neurotoxins/toxicity Rats Rats, Inbred Strains Scorpion Venoms/toxicity Sea Anemones Sodium/metabolism Tetrodotoxin/toxicity
Chemicals
Cnidarian Venoms Ion Channels Neurotoxins Scorpion Venoms Tetrodotoxin Sodium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Frelin C
Vigne P
Schweitz H
Lazdunski M
Article Info
Journal
Molecular pharmacology
Abbr.
Mol Pharmacol
ISSN
0026-895X
Published
1984-07-00
Pages
70-4
Language
English
Region
United States
NLM ID
0035623
Subset
IM
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