Kinin B1 receptors and the cardiovascular system:: regulation of expression and function

被引:104
作者
McLean, PG
Perretti, M
Ahluwalia, A
机构
[1] UCL, Rayne Inst, Dept Med, Ctr Clin Pharmacol, London WC1 E6JJ, England
[2] St Bartholomews & Royal London Sch Med & Dent, William Harvey Res Inst, Dept Biochem Pharmacol, London EC1 M6BQ, England
关键词
G-proteins; infection/inflammation; receptors; signal transduction;
D O I
10.1016/S0008-6363(00)00184-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Kinins are important peptide mediators of a diverse range of physiological and pathological functions of the cardiovascular system. The kinin peptides exert their effects by selective activation of two distinct C-protein coupled receptors termed B(1) and B(2). The principal kinin peptides involved in the acute regulation of cardiovascular function during normal physiology are bradykinin (BK) and Lys-BK which produce their effects via activation of B(2) receptors. The B(1) receptor is activated by the des-Arg(9)kinin metabolites namely des-Arg(9)BK and Lys-des-Arg(9)BK, the synthesis of which are increased during inflammation. The B(1) receptor, which is not constitutively expressed, is induced in various pathologies relating to inflammation. Recent investigations into the molecular mechanisms of B(1) receptor induction and their distribution and function in the cardiovascular system have shown that following an inflammatory stimulus the B(1) receptor is induced and may play an important role in modulation of cardiovascular function. This review summarises recent studies on B(1) receptor expression and function in the cardiovascular system and discusses the role of these receptors in regulation of circulatory homeostasis and their potential as therapeutic targets. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:194 / 210
页数:17
相关论文
共 173 条
[1]   Characterisation of kinin receptors on the human isolated umbilical artery [J].
Abbas, F ;
Clayton, JK ;
Marshall, KM ;
Senior, J .
JOURNAL OF ENDOCRINOLOGY, 1998, 156 (02) :389-394
[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]   INVESTIGATIONS INTO THE MECHANISM OF VASOCONSTRICTOR ACTION OF THE TOPICAL STEROID BETAMETHASONE-17-VALERATE IN THE RAT [J].
AHLUWALIA, A ;
FLOWER, RJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (02) :544-548
[4]  
Ahluwalia A, 1996, J IMMUNOL, V156, P269
[5]   Salt-sensitive hypertension in bradykinin B-2 receptor knockout mice [J].
Alfie, ME ;
Yang, XP ;
Hess, F ;
Carretero, OA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 224 (03) :625-630
[6]   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
[7]   CENTRAL BRADYKININERGIC SYSTEM IN NORMOTENSIVE AND HYPERTENSIVE RATS [J].
ALVAREZ, AL ;
DELORENZI, A ;
SANTAJULIANA, D ;
FINKIELMAN, S ;
NAHMOD, VE ;
PIROLA, CJ .
CLINICAL SCIENCE, 1992, 82 (05) :513-519
[8]   ROLE OF H1 RECEPTORS AND P-SELECTIN IN HISTAMINE-INDUCED LEUKOCYTE ROLLING AND ADHESION IN POSTCAPILLARY VENULES [J].
ASAKO, H ;
KUROSE, I ;
WOLF, R ;
DEFREES, S ;
ZHENG, ZL ;
PHILLIPS, ML ;
PAULSON, JC ;
GRANGER, DN .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (04) :1508-1515
[9]  
Audet R, 1997, J PHARMACOL EXP THER, V280, P6
[10]  
Austin CE, 1997, J BIOL CHEM, V272, P11420