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PMID: 6294122 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Amiloride, protein synthesis, and activation of quiescent cells.

Journal of cellular physiology ·Vol. 113 ·No. 2 ·1982-11-00 ·Pages 247-51

Lubin M, Cahn F, Coutermarsh BA

Abstract

Amiloride is known to inhibit both influx of sodium ions and activation of quiescent cells by growth factors. The coincidence of these effects has been cited to support the proposal that influx of sodium ions acts as a mitogenic signal. Although it was noted that amiloride inhibited protein synthesis, this was attributed to an action on transport of amino acids, particularly those coupled to sodium fluxes. We find, however, that amiloride directly inhibits polypeptide synthesis in a reticulocyte lysate. In Swiss 3T3 cells, concentrations of amiloride and of cycloheximide that are nearly matched in their degree of inhibition of protein synthesis, produce about the same degree of inhibition of transit of cells from G0 to S. Inhibition of protein synthesis is sufficient to explain the effect of amiloride on mitogenesis; the drug, therefore, is not suitable for testing the hypothesis that sodium influx is a mitogenic signal.

MeSH Terms
Amiloride/pharmacology Amino Acids/metabolism Aminoisobutyric Acids/metabolism Animals Biological Transport/drug effects Cell Line Cell-Free System Cycloheximide/pharmacology Interphase/drug effects Mice Peptide Chain Elongation, Translational/drug effects Protein Biosynthesis Pyrazines/pharmacology Sodium/metabolism Sodium-Potassium-Exchanging ATPase/metabolism
Chemicals
Amino Acids Aminoisobutyric Acids Pyrazines Amiloride Cycloheximide Sodium Sodium-Potassium-Exchanging ATPase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lubin M
Cahn F
Coutermarsh B A
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
1982-11-00
Pages
247-51
Language
English
Region
United States
NLM ID
0050222
Subset
IM
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