Activation of the nicotinic acetylcholine receptor mobilizes calcium from caffeine-insensitive stores in C2C12 mouse myotubes

Pflugers Arch. 1993 Mar;422(6):591-8. doi: 10.1007/BF00374007.

Abstract

In cultured mouse C2C12 myotubes, digital Ca2+ imaging fluorescence microscopy using the acetoxymethyl ester of Fura-2, Fura-2-AM, showed that, in the absence of extracellular Ca2+, acetylcholine (ACh) and nicotine, but not muscarine, raised the intracellular concentration of Ca2+ ([Ca2+]i) by about tenfold. ACh-induced Ca2+ mobilization was prevented by thapsigargin, a drug known to deplete inositol 1,4,5-trisphosphate (InsP3)-sensitive stores, and was concomitant with InsP3 accumulation. Caffeine, which releases Ca2+ from the ryanodine-sensitive stores of the sarcoplasmic reticulum, did not interfere with the ACh-induced [Ca2+]i increase. Ca2+ mobilization was also inhibited when myotubes were depolarized by high K+, or when extracellular Na+ was omitted. Nicotinic ACh receptor (nAChR) stimulation lowered intracellular pH with a time course slower than the [Ca2+]i increase. Possible mechanisms linking the current flowing through the nAChR pore to [Ca2+]i increase are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Caffeine / pharmacology*
  • Calcium / metabolism*
  • Cell Line
  • Hydrogen-Ion Concentration
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Kinetics
  • Mice
  • Microscopy, Fluorescence
  • Muscles / drug effects
  • Muscles / metabolism*
  • Receptors, Nicotinic / physiology*
  • Sarcoplasmic Reticulum / drug effects
  • Sarcoplasmic Reticulum / metabolism
  • Terpenes / pharmacology
  • Thapsigargin

Substances

  • Receptors, Nicotinic
  • Terpenes
  • Caffeine
  • Thapsigargin
  • Inositol 1,4,5-Trisphosphate
  • Acetylcholine
  • Calcium