The kinin B1 receptor and inflammation: new therapeutic target for cardiovascular disease

被引:49
作者
Duchene, Johan [1 ]
Ahluwalia, Amrita [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, London EC1M 6BQ, England
基金
英国惠康基金;
关键词
ISCHEMIA-REPERFUSION INJURY; NF-KAPPA-B; BRADYKININ B1; NONPEPTIDE ANTAGONISTS; MOUSE PLEURISY; HIGH-RISK; MECHANISMS; EXPRESSION; ATHEROSCLEROSIS; NEUTROPHILS;
D O I
10.1016/j.coph.2008.11.011
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The kinin B, receptor plays an important role in mediating the inflammatory effects of the kallikrein-kinin pathway. The recent development of orally available non-peptidic antagonists and genetically modified mice deficient in B, receptor expression have demonstrated that the receptor plays a pivotal role in the cellular, particularly neutrophil, recruitment associated with an acute inflammatory response. These tools have also enabled elucidation of the pathways involved in mediating this effect and have highlighted a major role for chemokines, particularly CXCL5 and CCL2. Neutrophil recruitment is involved in the pathogenesis of renal disease and has very recently been implicated in the early stages of atherosclerosis. In this review we discuss the most recent evidence linking the B, receptor with the pathogenesis of these two inflammatory cardiovascular diseases and highlight the therapeutic potential of the kinin B, receptor in these disease states.
引用
收藏
页码:125 / 131
页数:7
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