Studies on the mechanism of PAF-induced vasopermeability in rat lungs

Prostaglandins Leukot Essent Fatty Acids. 1995 Apr;52(4):245-9. doi: 10.1016/0952-3278(95)90044-6.

Abstract

The present study evaluated the effect of platelet activating factor (PAF) instilled into rat airways on vascular permeability assessed in isolated lung tissues by Evans blue (EB)-labelled plasma protein extravasation. It was found that intratracheal instillation of PAF induces a dose-dependent increase of EB extravasation in the bronchi (upper and inner) but not in the lung parenchyma. The contribution of eicosanoids to PAF-induced increase of vascular permeability was investigated by treating the animals with selected inhibitors prior to PAF administration. Mepacrine (5 mg/kg), L-663,536 (10 mg/kg), indomethacin (4 mg/kg) and dazoxiben (10 mg/kg) significantly reduced EB extravasation in the bronchi. The PAF antagonists BN-52021 (5 mg/kg), WEB-2086 (1 mg/kg), WEB-2170 (5 mg/kg) and PCA-4248 (3 mg/kg) were all effective in reducing the extravasation. These results suggest that PAF-induced increase of vascular permeability in rat bronchi is mediated by cyclooxygenase and lipoxygenase products of arachidonic acid metabolism.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Proteins / metabolism
  • Bronchi / blood supply
  • Capillary Permeability / drug effects*
  • Evans Blue
  • Extravasation of Diagnostic and Therapeutic Materials
  • Imidazoles / pharmacology
  • Indomethacin / pharmacology
  • Lung / blood supply*
  • Male
  • Platelet Activating Factor / administration & dosage
  • Platelet Activating Factor / antagonists & inhibitors
  • Platelet Activating Factor / pharmacology*
  • Quinacrine / pharmacology
  • Rats
  • Rats, Wistar
  • Trachea

Substances

  • Blood Proteins
  • Imidazoles
  • Platelet Activating Factor
  • dazoxiben
  • Evans Blue
  • Quinacrine
  • Indomethacin