Possible involvement of Ca2+-independent phospholipase A2 in protease-activated receptor-2-mediated contraction of rat urinary bladder

Naunyn Schmiedebergs Arch Pharmacol. 2003 Jun;367(6):588-91. doi: 10.1007/s00210-003-0753-0. Epub 2003 May 15.

Abstract

Possible involvement of Ca(2+)-independent phospholipase A2 (iPLA2) was examined in protease-activated receptor-2 (PAR-2)-mediated contraction of the rat urinary bladder. Both PAR-2 activating peptide (PAR-2 AP; SLIGRL-NH2) and trypsin produced a concentration-dependent contractile response in the urinary bladder preparations. These contractions were significantly (p<0.01) attenuated by indomethacin (10 microM), an inhibitor of cyclooxygenase, or bromoenol lactone (BEL; 10 micro M), an inhibitor of iPLA2. On the other hand, the contractile responses to bradykinin were not significantly affected by BEL, although they were reduced by indomethacin. Arachidonyltrifluoromethyl ketone (AACOCF3; 30 microM), an inhibitor of cytosolic Ca(2+)-dependent phospholipase A2, did not affect the trypsin- and bradykinin-induced contractions. Both indomethacin and BEL had no inhibitory effect on the prostaglandin E2-induced contractions. These results suggest that PAR-2 activators and bradykinin stimulate the release of prostaglandins and thereby contract the rat urinary bladder smooth muscles. The release of prostaglandins by PAR-2 activators seems to be partly mediated by the iPLA2.

MeSH terms

  • Animals
  • Bradykinin / pharmacology
  • Dose-Response Relationship, Drug
  • Group VI Phospholipases A2
  • In Vitro Techniques
  • Male
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology*
  • Phospholipases A / physiology*
  • Phospholipases A2
  • Rats
  • Rats, Wistar
  • Receptor, PAR-2 / agonists
  • Receptor, PAR-2 / metabolism*
  • Trypsin / pharmacology
  • Urinary Bladder / enzymology*
  • Urinary Bladder / metabolism

Substances

  • Receptor, PAR-2
  • Phospholipases A
  • Group VI Phospholipases A2
  • Phospholipases A2
  • Trypsin
  • Bradykinin