Induction of Na+/K(+)-ATPase activity by long-term stimulation of nicotinic acetylcholine receptors in C2C12 myotubes

Br J Pharmacol. 1994 Feb;111(2):459-64. doi: 10.1111/j.1476-5381.1994.tb14758.x.

Abstract

1. To investigate the role of long-term stimulation of nicotinic acetylcholine receptors (AChRs) on the regulation of membrane potential, non-contracting C2C12 myotubes were stimulated for 1-4 days with carbachol (10 microM) and membrane potentials were measured by the intracellular microelectrode technique after washing out of the drug. 2. The membrane potential (-45.7 mV) gradually increased by 10.1 mV to -55.8 mV during 4 days treatment, which was caused by enhanced electrogenic Na+/K(+)-pumping. 3. The concentration-dependent enhancement of Na+/K(+)-ATPase activity in long-term carbachol-treated myotubes (4 days, EC50 = 5.3 microM) was prevented by co-treatment with the competitive nicotinic AChR antagonist, pancuronium but not by the muscarinic antagonist, atropine. 4. Enhanced Na+/K(+)-ATPase activity still developed in carbachol-stimulated myotubes during co-treatment (4 days) with the nicotinic AChR-channel blocker, chlorpromazine (1 microM). Membrane depolarization as such, obtained by incubation in high K+ medium (40 mM, 4 days) did not enhance Na+/K(+)-ATPase activity. 5. Non-treated myotubes possessed a high-affinity ouabain binding site (Kd = 119 nM) in association with the low Na+/K(+)-pumping activity. Long-term stimulation of myotubes (4 days) with carbachol or with a combination of carbachol and chlorpromazine was accompanied by the development of an additional low-affinity ouabain binding site (Kd = 13 microM). 6. Binding of monoclonal antibodies directed against either alpha 1- or alpha 2-subunit of Na+/K(+)-ATPase were both increased in myotubes treated with carbachol (4 days). 7. These results support the concept that nicotinic AChRs regulate Na+/K(+)-ATPase activity, independent of the functionality of the receptor-operated ion-channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Carbachol / pharmacology
  • Cell Line
  • Cholinergic Antagonists
  • Electrophysiology
  • Enzyme Induction / drug effects
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Mice
  • Microtubules / drug effects
  • Microtubules / enzymology*
  • Muscles / drug effects
  • Muscles / enzymology*
  • Muscles / ultrastructure
  • Ouabain / pharmacokinetics
  • Receptors, Cholinergic / drug effects
  • Receptors, Cholinergic / metabolism*
  • Sodium-Potassium-Exchanging ATPase / biosynthesis*
  • Sodium-Potassium-Exchanging ATPase / immunology
  • Up-Regulation / drug effects

Substances

  • Antibodies, Monoclonal
  • Cholinergic Antagonists
  • Receptors, Cholinergic
  • Ouabain
  • Carbachol
  • Sodium-Potassium-Exchanging ATPase