Neurotransmitters involved in the fast inhibitory junction potentials in mouse distal colon

Eur J Pharmacol. 2003 Jan 24;460(2-3):183-90. doi: 10.1016/s0014-2999(02)02923-0.

Abstract

We investigated, in murine colon circular muscle, the role of adenosine 5'-triphosphate (ATP) and pituitary adenylate cyclase activating peptide (PACAP) as inhibitory neurotransmitters of the fast component of nerve-evoked inhibitory junction potential (fast IJP). Fast IJP was antagonised by apamin or suramin, abolished by desensitisation with the P2Y receptor agonist, adenosine 5'-O-2-thiodiphosphate (ADPbetaS), unaffected by desensitisation with P2X receptor agonist, alpha,beta-methylene ATP (alpha,beta-meATP), and reduced by PACAP-(6-38), a PACAP receptor antagonist. ATP induced membrane hyperpolarization resistant to tetrodotoxin, N(omega)-nitro-L-arginine methyl ester (L-NAME) or PACAP-(6-38), but antagonised by apamin, suramin, P2X and P2Y receptor desensitisation. PACAP-(1-27) caused membrane hyperpolarization antagonised by PACAP-(6-38), apamin and P2Y receptor desensitisation, reduced by tetrodotoxin, but not affected by L-NAME and by P2X receptor desensitisation. Therefore, in murine colon circular muscle, an ATP-like endogenous P2Y purinoceptor ligand is the final nonadrenergic, noncholinergic (NANC) inhibitory mediator involved in the generation of fast IJP. A neuromodulator role of PACAP in the inhibitory pathway is supposed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Diphosphate / analogs & derivatives*
  • Adenosine Diphosphate / pharmacology
  • Adenosine Triphosphate / analogs & derivatives*
  • Adenosine Triphosphate / pharmacology
  • Animals
  • Apamin / pharmacology
  • Colon / cytology
  • Colon / drug effects*
  • Colon / physiology
  • Dose-Response Relationship, Drug
  • Male
  • Membrane Potentials / drug effects
  • Mice
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Neuromuscular Junction / drug effects*
  • Neuromuscular Junction / physiology
  • Neuropeptides / pharmacology
  • Neurotransmitter Agents / pharmacology*
  • Peptide Fragments / pharmacology
  • Pituitary Adenylate Cyclase-Activating Polypeptide
  • Suramin / pharmacology
  • Tetrodotoxin / pharmacology
  • Thionucleotides / pharmacology

Substances

  • Adcyap1 protein, mouse
  • Neuropeptides
  • Neurotransmitter Agents
  • Peptide Fragments
  • Pituitary Adenylate Cyclase-Activating Polypeptide
  • Thionucleotides
  • pituitary adenylate-cyclase-activating-peptide (6-38)
  • Apamin
  • adenosine 5'-O-(2-thiodiphosphate)
  • Tetrodotoxin
  • Suramin
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • alpha,beta-methyleneadenosine 5'-triphosphate
  • NG-Nitroarginine Methyl Ester

Grants and funding