Muscarinic M2 receptors inhibit Ca2+-activated K+ channels in rat bladder smooth muscle

Int J Urol. 2002 Dec;9(12):689-96. doi: 10.1046/j.1442-2042.2002.00548.x.

Abstract

Purpose: To clarify the functional relationship between M2 muscarinic receptor and Ca2+-activated K+ channel, we investigated the effect of carbachol (CCh) on the membrane current of rat bladder smooth muscle cells.

Methods: Rat bladder single smooth muscle cells were patch clamped with whole-cell configuration.

Results: CCh (10 micro mol/L) transiently induced an outward current in the presence of K+ in the pipette solution. A high Ca2+ concentration in the pipette solution persistently induced an outward current, which was inhibited by CCh. In the presence of M2 inhibitor, AFDX-384, CCh induced the outward current persistently, indicating that M2 was involved in the current inhibition. In pertussis toxin pretreated cells, CCh did not apparently inhibit the outward current. The CCh-induced outward current was inhibited by iberiotoxin, a selective inhibitor of large-conductance Ca2+-activated K+ channels (BKCa).

Conclusion: CCh induces BKCa, which is inhibited by M2- and Gi-mediated signal transduction pathway. This M2-mediated pathway may enhance contraction which is initiated by M3-stimulation in rat bladder smooth muscle.

MeSH terms

  • Animals
  • Carbachol / pharmacology
  • Male
  • Muscle, Smooth / drug effects
  • Muscle, Smooth / physiology*
  • Peptides / pharmacology
  • Pertussis Toxin / pharmacology
  • Potassium Channels, Calcium-Activated / antagonists & inhibitors
  • Potassium Channels, Calcium-Activated / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Muscarinic M2
  • Receptors, Muscarinic / physiology*
  • Toxins, Biological / pharmacology
  • Urinary Bladder / drug effects
  • Urinary Bladder / physiology*

Substances

  • Peptides
  • Potassium Channels, Calcium-Activated
  • Receptor, Muscarinic M2
  • Receptors, Muscarinic
  • Toxins, Biological
  • iberiotoxin
  • Carbachol
  • Pertussis Toxin