Pardaxin produces postjunctional muscle contraction in guinea-pig intestinal smooth muscle

Br J Pharmacol. 1984 May;82(1):43-9. doi: 10.1111/j.1476-5381.1984.tb16440.x.

Abstract

The action of pardaxin (PX), a toxin isolated from the secretion of the Red Sea flatfish, Pardachirus marmoratus, was studied on longitudinal muscle of guinea-pig ileum. Pardaxin contracted the ileum and subsequently abolished muscle contraction to 5-hydroxytryptamine (5-HT), but did not affect the responses to acetylcholine (ACh) and substance P(SP). Pardaxin-induced contraction was only partially suppressed by atropine and not affected by tetrodotoxin or morphine. Preparations desensitized to 5-HT or SP responded normally to pardaxin. Pardaxin-induced contractions were normal in K+-depolarizing Krebs Ringer solution and not affected by black widow spider venom. It is concluded that the pardaxin-induced muscle contractions are not mediated through the release of neurotransmitters and do not involve 5-HT, SP or ACh receptors, but are due to a direct action on the muscle contractile mechanism.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Diphenhydramine / pharmacology
  • Drug Interactions
  • Electric Stimulation
  • Fish Venoms / pharmacology*
  • Guinea Pigs
  • In Vitro Techniques
  • Isometric Contraction
  • Morphine / pharmacology
  • Muscle Contraction / drug effects
  • Muscle, Smooth / drug effects*
  • Nicotine / pharmacology
  • Physostigmine / pharmacology
  • Serotonin / pharmacology
  • Spider Venoms / pharmacology
  • Substance P / pharmacology

Substances

  • Fish Venoms
  • Spider Venoms
  • Serotonin
  • Substance P
  • pardaxin
  • Nicotine
  • Morphine
  • Diphenhydramine
  • Physostigmine
  • Acetylcholine
  • black widow spider venom