Modulation of allergic and immune complex-induced lung inflammation by bradykinin receptor antagonists

被引:22
|
作者
Landgraf, RG
Steil, AA
Sirois, P
Jancar, S
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil
[2] Univ Vale Itajai, Itajai, SC, Brazil
[3] Univ Sherbrooke, Sch Med, Inst Pharmacol, Sherbrooke, PQ J1K 2R1, Canada
基金
巴西圣保罗研究基金会;
关键词
bradykinin; bradykinin receptor antagonist; lung inflammation; asthma; immune complexes;
D O I
10.1007/s00011-003-1226-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: The effect of bradykinin (13, or B,) receptor antagonists was studied in allergic and immune-complex-induced lung inflammation. Methods: Lungs of BALB/c mice were examined 24 It after induction of lung inflammation, either allergic (ovalbumin-sensitized submitted to two aerosol of antigen, one week apart) or immune-complex induced (intratracheal instillation of IgG antibodies followed by intravenous antigen). The bradykinin 13, receptor antagonist, HOE-140 or bradykinin B, receptor antagonist, R-954 were given intraperitoneally (100 mug/kg), 30 min before induction. Results: In allergic inflammation, pre-treatment with R-954 reduced eosinophil infiltration into the lungs, mucus secretion and the airway hyperreactivity to methacholine. Pretreatment with HOE-140 increased eosinophil infiltration but did not affect the other parameters. In immune-complex inflammation, HOE-140 increased neutrophil infiltration but not their activation nor the hemorrhagic lesions. R-594. pretreatment did not change the parameters examined. Conclusion: These results show important modulatory effects of bradykinin 13, and B, receptor antagonists in both models of lung inflammation.
引用
收藏
页码:78 / 83
页数:6
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