Is muscular acetylcholinesterase activity correlated with the intracellular concentration of free calcium?

The role of the calcium ion Ca2+ as an agent of intracellular control in a variety of physiological processes is well established. In vertebrate skeletal muscle fibers, Ca2+ is involved in muscle contraction, modulation of membrane permeability and regulation of metabolic activity. Recently it was s...

Full description

Saved in:
Bibliographic Details
Published inReproduction, nutrition, développement Vol. 28; no. 3B; p. 785
Main Authors de la Porte, S, Courbin, P, Grouselle, M, Duflo, D, Desmazes, J P, Georgescauld, D, Koenig, J
Format Journal Article
LanguageFrench
Published France 1988
Subjects
Acetylcholinesterase - metabolism
Aminoquinolines
Animals
Calcimycin - pharmacology
Calcium - metabolism
Cell Differentiation
Cell Membrane Permeability - drug effects
Ethers - pharmacology
Fluorescent Dyes
Ionomycin
Membrane Potentials - drug effects
Muscles - embryology
Muscles - metabolism
Potassium Chloride - pharmacology
Rats
Tetrodotoxin - pharmacology
Veratridine - pharmacology
Online AccessGet full text

Cover

More Information
Summary:The role of the calcium ion Ca2+ as an agent of intracellular control in a variety of physiological processes is well established. In vertebrate skeletal muscle fibers, Ca2+ is involved in muscle contraction, modulation of membrane permeability and regulation of metabolic activity. Recently it was suggested that ion fluxes through membranes regulate the level of two cholinergic macromolecules, the acetylcholine receptor and the A12 form of acetylcholinesterase (AChE), the presumed synaptic form of the enzyme. Muscle cells paralysed by veratridine, which maintains the Na+ channel in the open state, showed an increase in total AChE and in the levels of the A12 form. The effect of veratridine on AChE was blocked in the presence of agents that block Ca2+ permeability suggesting that Ca2+ is involved in this effect. To understand whether the level of muscle AChE is related in some way to the level of free intracellular Ca2+, we analysed the variations of Ca2+ levels in rat muscle cells treated by agents which modify the ionic permeabilities. This level was determined by spectrofluorimetry using the fluorescent Ca2+ indicator: Quin 2. However no correlation between these parameters was observed in our experimental conditions.
ISSN:0181-1916