Pharmacological modulation of the contractile response to toluene diisocyanate in the rat isolated urinary bladder

Br J Pharmacol. 1990 Aug;100(4):886-8. doi: 10.1111/j.1476-5381.1990.tb14109.x.

Abstract

1. Toluene diisocyanate produced concentration-dependent contractions of the rat isolated urinary bladder. 2. The contractions were tetrodotoxin-resistant and were abolished by previous exposure of the strips to capsaicin. 3. Indomethacin (5 microM) and ruthenium red (30 microM) inhibited toluene diisocyanate-induced contractions. Responses expressed as a percentage of the response obtained with substance P, 30 nM, were respectively 141.6 +/- 24.8% and 20.1 +/- 5.1% in control and indomethacin-treated strips (P less than 0.005); 123.0 +/- 30.2% and 14.0 +/- 6.5% in control and ruthenium red-treated strips (0.01 less than P less than 0.05). 4. These results suggest that toluene diisocyanate-induced contractions of the rat isolated bladder are the result of the release of cyclo-oxygenase products which may act by activating the capsaicin receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atropine / pharmacology
  • Capsaicin / pharmacology
  • In Vitro Techniques
  • Indomethacin / pharmacology
  • Male
  • Methylprednisolone / pharmacology
  • Muscle Contraction / drug effects
  • Muscle, Smooth / drug effects*
  • Rats
  • Rats, Inbred Strains
  • Ruthenium Red / pharmacology
  • Tetrodotoxin / pharmacology
  • Toluene 2,4-Diisocyanate / pharmacology*
  • Urinary Bladder / drug effects

Substances

  • Ruthenium Red
  • Toluene 2,4-Diisocyanate
  • Tetrodotoxin
  • Atropine
  • Capsaicin
  • Methylprednisolone
  • Indomethacin