Pre-junctional muscarinic autoreceptors in bovine airways

Respir Physiol Neurobiol. 2012 Jan 15;180(1):45-51. doi: 10.1016/j.resp.2011.10.007. Epub 2011 Oct 17.

Abstract

We searched for pre-junctional inhibitory muscarinic receptors in isolated bovine trachealis strips and bronchial rings. Electric stimulation (ES)-induced tritiated acetylcholine ([(3)H]-ACh)-release and isometric contractions were determined in muscles incubated with the non-selective muscarinic agonist pilocarpine, the non-selective muscarinic antagonist atropine, the selective M(2)-receptor antagonists methoctramine and gallamine, or the selective M(4)-receptor antagonist PD102807. Electric field stimulation (EFS)-induced isometric contractile responses were assessed in trachealis strips and bronchial rings treated with 10(-9)-10(-5)M methoctramine, gallamine or PD102807. Pilocarpine (10(-6) and 10(-5)M) and atropine (10(-7)M) significantly decreased and increased ES-evoked [(3)H]-ACh-release, respectively. The enhancing effect of atropine on [(3)H]-ACh-release prevailed over the inhibitory effect of pilocarpine. M(2)- and M(4)-receptor antagonists did not increase EFS-induced contraction or ES-induced [(3)H]-ACh-release. However, 10(-7)M methoctramine, gallamine or PD102807 significantly attenuated the inhibitory effects of pilocarpine 10(-5)M on ES-induced [(3)H]-ACh-release.

Conclusions: Muscarinic autoregulation is present in bovine airways but is not fully accounted for by M(2)- and M(4)-receptor subtypes.

MeSH terms

  • Animals
  • Autoreceptors / biosynthesis*
  • Autoreceptors / drug effects
  • Bronchi / drug effects
  • Bronchi / metabolism*
  • Cattle
  • Electric Stimulation
  • Muscarinic Agonists / pharmacology
  • Muscarinic Antagonists / pharmacology
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology
  • Muscle, Smooth / drug effects
  • Muscle, Smooth / metabolism
  • Receptors, Muscarinic / biosynthesis*
  • Trachea / drug effects
  • Trachea / metabolism*

Substances

  • Autoreceptors
  • Muscarinic Agonists
  • Muscarinic Antagonists
  • Receptors, Muscarinic