Targeting the bradykinin B1 receptor to reduce pain

被引:33
作者
Chen, Jian Jeffrey [1 ]
Johnson, Eileen J. [1 ]
机构
[1] Amgen Inc, Chem Res & Dev, Thousand Oaks, CA 91320 USA
关键词
KININ B-1 RECEPTORS; PROTEIN-COUPLED RECEPTORS; PHARMACOLOGICAL CHARACTERIZATION; UP-REGULATION; MECHANICAL HYPERALGESIA; MYOCARDIAL-INFARCTION; NONPEPTIDE ANTAGONIST; THERMAL HYPERALGESIA; GENE-EXPRESSION; MESSENGER-RNA;
D O I
10.1517/14728222.11.1.21
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The bradykinin B1 receptor is an inducible G-protein-coupled receptor. it is induced or upregulated at the site of inflammation or injury. A large body of preclinical data supports the development of B1 antagonists as novel therapeutics for the treatment of pain and inflammation. The necessary in vitro and in vivo drug discovery tools are currently available to evaluate novel B1 antagonists. Two major classes of small-molecule B1 antagonists, arylsulfonamide-based and biphenyl-based Ell antagonists, have been disclosed in the last few years.
引用
收藏
页码:21 / 35
页数:15
相关论文
共 106 条
[1]   Bradykinin B1 receptor mediates inhibition of neointima formation in rat artery after balloon angioplasty [J].
Agata, J ;
Miao, RQ ;
Yayama, K ;
Chao, L ;
Chao, J .
HYPERTENSION, 2000, 36 (03) :364-370
[2]   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
[3]   Effect of high salt intake in mutant mice lacking bradykinin-B-2 receptors [J].
Alfie, ME ;
Sigmon, DH ;
Pomposiello, SI ;
Carretero, OA .
HYPERTENSION, 1997, 29 (01) :483-487
[4]  
AMG INC, 2004, Patent No. 2004092164
[5]  
AMG INC, 2006, Patent No. 2006036664
[6]  
AMG INC, 2006, Patent No. 2006044412
[7]  
AMG INC, 2005, Patent No. 25014791
[8]  
AMGEN INC, 2004, Patent No. 2004092116
[9]  
Anthony N.J., 2005, [No title captured], Patent No. [WO/2005/004810, 2005004810]
[10]   Altered neutrophil homeostasis in kinin B1 receptor-deficient mice [J].
Araújo, RC ;
Kettritz, R ;
Fichtner, I ;
Paiva, ACM ;
Pesquero, JB ;
Bader, M .
BIOLOGICAL CHEMISTRY, 2001, 382 (01) :91-95