Targeting kinin receptors for the treatment of tissue ischaemia

被引:37
作者
Emanueli, C [1 ]
Madeddu, P
机构
[1] Natl Inst Biostruct & Biosyst, Natl Lab, Cardiovasc Med & Gene Therapy Sect, Osilo, Italy
[2] Med Univ Sassari, Dept Internal Med, Sassari, Italy
关键词
D O I
10.1016/S0165-6147(00)01761-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Kinins, the biological end-products of the kallikrein-kininogen system, influence many aspects of the cellular function. Interest in this peptidergic system has been renewed recently by the discovery that kinins exert cardiovascular protective effects and promote post-ischaemic recovery by stimulating vascular growth. Pharmacological and genetic studies indicate that induction of kallikrein and kinin receptors by ischaemia is functionally relevant in the natural host response that permits perfusion recovery and tissue healing. Furthermore, potentiation of the generation of kinins by continuous supply of tissue kallikrein promotes reparative angiogenesis through stimulation of the release of nitric oxide and prostaglandins. Strategies that activate kinin receptors might be applicable to the treatment of occlusive vascular disease, whereas kinin receptor antagonists could represent therapeutic reagents against pathological angiogenesis in cancer and chronic inflammatory conditions.
引用
收藏
页码:478 / 484
页数:7
相关论文
共 68 条
[1]   B1 receptors as a new inflammatory target.: Could this B the 1? [J].
Ahluwalia, A ;
Perretti, M .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1999, 20 (03) :100-104
[2]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[3]   EFFECTS OF ACIDIC FIBROBLAST GROWTH-FACTOR ON NORMAL AND ISCHEMIC MYOCARDIUM [J].
BANAI, S ;
JAKLITSCH, MT ;
CASSCELLS, W ;
SHOU, M ;
SHRIVASTAV, S ;
CORREA, R ;
EPSTEIN, SE ;
UNGER, EF .
CIRCULATION RESEARCH, 1991, 69 (01) :76-85
[4]   Constitutive expression of phVEGF165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia [J].
Baumgartner, I ;
Pieczek, A ;
Manor, O ;
Blair, R ;
Kearney, M ;
Walsh, K ;
Isner, JM .
CIRCULATION, 1998, 97 (12) :1114-1123
[5]  
BHOOLA KD, 1992, PHARMACOL REV, V44, P1
[6]   Role of kinins in the endothelial protective effect of ischaemic preconditioning [J].
Bouchard, JF ;
Chouinard, J ;
Lamontagne, D .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 123 (03) :413-420
[7]   Mechanisms of angiogenesis and arteriogenesis [J].
Carmeliet, P .
NATURE MEDICINE, 2000, 6 (04) :389-395
[8]   Novel roles of Kallistatin, a specific tissue kallikrein inhibitor, in vascular remodeling [J].
Chao, J ;
Miao, RQ ;
Chen, V ;
Chen, LM ;
Chao, L .
BIOLOGICAL CHEMISTRY, 2001, 382 (01) :15-21
[9]   A positively charged loop on the surface of kallistatin functions to enhance tissue kallikrein inhibition by acting as a secondary binding site for kallikrein [J].
Chen, VC ;
Chao, L ;
Chao, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (51) :40371-40377
[10]   Impaired collateral vessel development associated with reduced expression of vascular endothelial growth factor in ApoE-/- mice [J].
Couffinhal, T ;
Silver, M ;
Kearney, M ;
Sullivan, A ;
Witzenbichler, B ;
Magner, M ;
Annex, B ;
Peters, K ;
Isner, JM .
CIRCULATION, 1999, 99 (24) :3188-3198