The Renin-Angiotensin System: Emerging Concepts

被引:4
作者
Santos, Robson A. S. [1 ]
Campagnole-Santos, Maria Jose [1 ]
Pinheiro, Sergio V. B. [3 ]
Ferreira, Anderson J. [2 ]
机构
[1] Univ Fed Minas Gerais, Biol Sci Inst, Dept Physiol & Biophys, Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Biol Sci Inst, Dept Morphol, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Dept Pediat, Belo Horizonte, MG, Brazil
关键词
Angiotensin-(1-7); angiotensin IV; angiotensin-(1-7) receptor mas; angiotensin-converting enzyme 2;
D O I
10.2174/157340206778132617
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The renin-angiotensin system (RAS) is a pivotal regulator of the renal and cardiovascular functions playing an important role in the control of blood pressure and hydroelectrolyte balance. In the past few years the combination of classical physiopharmacological techniques with modern genomics and protein chemistry methods has lead to the identification of important novel components of the RAS: the Angiotensin (Ang) IV binding site IRAP (insulin-regulated aminopeptidase), the angiotensin-converting enzyme 2 (ACE2), and the Ang-(1-7) receptor Mas. Ang-(1-7) is one of the most interesting peptide fragments of the RAS because it has actions which are often opposite to those of Ang II. The recent identification of the Ang-(1-7) forming enzyme ACE2 and of Mas as an Ang-(1-7) receptor has added further support and more widely acceptance to a new concept of the RAS in which the system has two major arms: a vasoconstrictor/proliferative in which the major player is Ang II and a vasodilator/anti-proliferative in which the major effector is Ang-(1-7). In this article we will briefly review these novel aspects related to the RAS with focus on the possible physiological role of the ACE2-Ang-(1-7)-Mas axis in the cardiovascular system.
引用
收藏
页码:219 / 226
页数:8
相关论文
共 122 条
[1]   Evidence that the angiotensin IV (AT4) receptor is the enzyme insulin-regulated aminopeptidase [J].
Albiston, AL ;
McDowall, SG ;
Matsacos, D ;
Sim, P ;
Clune, E ;
Mustafa, T ;
Lee, J ;
Mendelsohn, FAO ;
Simpson, RJ ;
Connolly, LM ;
Chai, SY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (52) :48623-48626
[2]   Angiotensin-(1-7) potentiates the coronary vasodilatatory effect of bradykinin in the isolated rat heart [J].
Almeida, AP ;
Frábregas, BC ;
Madureira, MM ;
Santos, RJS ;
Campagnole-Santos, MJ ;
Santos, RAS .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2000, 33 (06) :709-713
[3]   [7-D-ALA]-ANGIOTENSIN-(1-7) - SELECTIVE ANTAGONISM OF ANGIOTENSIN-(1-7) IN THE RAT PARAVENTRICULAR NUCLEUS [J].
AMBUHL, P ;
FELIX, D ;
KHOSLA, MC .
BRAIN RESEARCH BULLETIN, 1994, 35 (04) :289-291
[4]   Physiology - Two ACEs and a heart [J].
Bernstein, KE .
NATURE, 2002, 417 (6891) :799-802
[5]   Angiotensin-converting enzyme 2 - A new cardiac regulator [J].
Boehm, M ;
Nabel, EG .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (22) :1795-1797
[6]  
Brosnihan KB, 2003, HYPERTENSION, V42, P749, DOI 10.1161/01.HYP.0000085220.53285.11
[7]   Angiotensin-(1-7) dilates canine coronary arteries through kinins and nitric oxide [J].
Brosnihan, KB ;
Li, P ;
Ferrario, CM .
HYPERTENSION, 1996, 27 (03) :523-528
[8]   ACE2, a new regulator of the renin-angiotensin system [J].
Burrell, LM ;
Johnston, CI ;
Tikellis, C ;
Cooper, ME .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2004, 15 (04) :166-169
[9]   RETENTION OF CEREBROVASCULAR DILATION AFTER CORTICAL SPREADING DEPRESSION IN ANESTHETIZED RABBITS [J].
BUSIJA, DW ;
MENG, W .
STROKE, 1993, 24 (11) :1740-1745
[10]   DIFFERENTIAL BARORECEPTOR REFLEX MODULATION BY CENTRALLY INFUSED ANGIOTENSIN PEPTIDES [J].
CAMPAGNOLESANTOS, MJ ;
HERINGER, SB ;
BATISTA, EN ;
KHOSLA, MC ;
SANTOS, RAS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :R89-R97