Contractile effects of substance P and neurokinin A on the rat stomach in vivo and in vitro

Br J Pharmacol. 1987 Jan;90(1):273-9. doi: 10.1111/j.1476-5381.1987.tb16849.x.

Abstract

Substance P and neurokinin A (substance K) were infused into the coeliac artery of anaesthetized rats at doses of 0.06-20 nmol min-1. Both tachykinins caused contractions of the stomach, the threshold dose of neurokinin A being 10 times lower than of substance P. The dose-response curve for substance P was flatter than that for neurokinin A. On circular muscle strips from the rat gastric corpus in vitro, the dose-response curves for both tachykinins were parallel, neurokinin A being 10 times more potent than substance P. The contractions in response to 10 microM neurokinin A and to 30 microM substance P were 58 and 54%, respectively, of the maximal contraction to bethanechol (1 mM). The effect of substance P was reduced by atropine both in vivo and in vitro. In vitro, the contractions to substance P were also reduced by tetrodotoxin but left unaffected by methysergide. The action of neurokinin A was not affected by these drugs. It is concluded that neurokinin A contracts rat stomach by a direct action on the circular smooth muscle, whereas the action of substance P is mediated, at least in part, by cholinergic interneurones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atropine / pharmacology
  • Bethanechol
  • Bethanechol Compounds / pharmacology
  • Female
  • Gastrointestinal Motility / drug effects*
  • Guanethidine / pharmacology
  • In Vitro Techniques
  • Male
  • Neurokinin A
  • Neuropeptides / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Substance P / pharmacology*
  • Tetrodotoxin / pharmacology

Substances

  • Bethanechol Compounds
  • Neuropeptides
  • Bethanechol
  • Substance P
  • Tetrodotoxin
  • Atropine
  • Neurokinin A
  • Guanethidine