Journal
PHARMACOLOGY
Volume 89, Issue 5-6, Pages 275-282Publisher
KARGER
DOI: 10.1159/000337378
Keywords
Proteinase-activated receptor-4; Neutrophils; Neutrophils recruitment; Pleurisy
Categories
Funding
- Fundacao de Amparo a Pesquisa de Minas Gerais (FAPEMIG)
- Conselho Nacional de Pesquisa e Desenvolvimento (CNPq)/Brazil
Ask authors/readers for more resources
Background/Aims: The activation of proteinase-activated receptors (PARs) has been implicated in the development of important hallmarks of inflammation, including in vivo leukocyte recruitment. Here, we examined the effects of aprotinin, a potent inhibitor of trypsin proteinase and the kallikrein-kinin system, and the PAR-4 antagonist YPGKF-NH2 (tcY-NH2) on neutrophil recruitment in response to carrageenan and trypsin in the pleural cavity of mice. Methods: BALB/c mice were intrapleurally injected with trypsin or PAR-4-activating peptide AY-NH2, pretreated with aprotinin or tcY-NH2 (1 mu g/cavity) prior to an intrapleural injection of trypsin or carrageenan, or pretreated with leukotriene B-4 antagonist U-75302 (3 mu g/cavity) prior to a trypsin injection. The number of infiltrating neutrophils was evaluated after 4 h. Results: PAR-4-activating peptide AY-NH2 and trypsin-induced neutrophil recruitment was inhibited by aprotinin, tcY-NH2 or U-75302. Aprotinin and tcY-NH2 also inhibited neutrophil recruitment induced by carrageenan. Conclusion: These data suggest a key role for PAR-4 in mediating neutrophil recruitment in a mouse model of pleurisy induced by the activity of trypsin or trypsin-like enzymes. copyright (C) 2012 S. Karger AG, Basel
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available