Physiology of local renin-angiotensin systems

被引:1329
作者
Paul, Martin [1 ]
Mehr, Ali Poyan [1 ]
Kreutz, Reinhold [1 ]
机构
[1] Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, D-12200 Berlin, Germany
关键词
D O I
10.1152/physrev.00036.2005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Physiology of Local Renin-Angiotensin Systems. Physiol Rev 86: 747-803, 2006; doi: 10.1152/physrev. 00036.2005.-Since the first identification of renin by Tigerstedt and Bergmann in 1898, the renin-angiotensin system (RAS) has been extensively studied. The current view of the system is characterized by an increased complexity, as evidenced by the discovery of new functional components and pathways of the RAS. In recent years, the pathophysiological implications of the system have been the main focus of attention, and inhibitors of the RAS such as angiotensin-converting enzyme (ACE) inhibitors and angiotensin (ANG) II receptor blockers have become important clinical tools in the treatment of cardiovascular and renal diseases such as hypertension, heart failure, and diabetic nephropathy. Nevertheless, the tissue RAS also plays an important role in mediating diverse physiological functions. These focus not only on the classical actions of ANG on the cardiovascular system, namely, the maintenance of cardiovascular homeostasis, but also on other functions. Recently, the research efforts studying these noncardiovascular effects of the RAS have intensified, and a large body of data are now available to support the existence of numerous organ-based RAS exerting diverse physiological effects. ANG II has direct effects at the cellular level and can influence, for example, cell growth and differentiation, but also may play a role as a mediator of apoptosis. These universal paracrine and autocrine actions may be important in many organ systems and can mediate important physiological stimuli. Transgenic overexpression and knock-out strategies of RAS genes in animals have also shown a central functional role of the RAS in prenatal development. Taken together, these findings may become increasingly important in the study of organ physiology but also for a fresh look at the implications of these findings for organ pathophysiology.
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页码:747 / 803
页数:57
相关论文
共 808 条
[41]   Behavioral effects of angiotensin II microinjected into CA1 hippocampal area [J].
Belcheva, I ;
Georgiev, V ;
Chobanova, M ;
Hadjiivanova, C .
NEUROPEPTIDES, 1997, 31 (01) :60-64
[42]   Differential behavioral effects of angiotensin II microinjected unilaterally into the CA1 hippocampal area [J].
Belcheva, I ;
Chobanova, M ;
Georgiev, V .
REGULATORY PEPTIDES, 1998, 74 (2-3) :67-71
[43]   Lateralized learning and memory effects of angiotensin II microinjected into the rat CA1 hippocampal area [J].
Belcheva, I ;
Ternianov, A ;
Georgiev, V .
PEPTIDES, 2000, 21 (03) :407-411
[44]   Immunohistochemical localization of the angiotensin II type 1 receptor in human hypothalamus and brainstem [J].
Benarroch, EE ;
Schmeichel, AM .
BRAIN RESEARCH, 1998, 812 (1-2) :292-296
[45]   IMMUNOHISTOCHEMICAL LOCALIZATION OF 2 ANGIOTENSIN I-CONVERTING ISOENZYMES IN THE REPRODUCTIVE-TRACT OF THE MALE RABBIT [J].
BERG, T ;
SULNER, J ;
LAI, CY ;
SOFFER, RL .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1986, 34 (06) :753-760
[46]   Flow-dependent dilation mediated by endogenous kinins requires angiotensin AT2 receptors [J].
Bergaya, S ;
Hilgers, RHP ;
Meneton, P ;
Dong, Y ;
Bloch-Faure, M ;
Inagami, T ;
Alhenc-Gelas, F ;
Lévy, BI ;
Boulanger, CM .
CIRCULATION RESEARCH, 2004, 94 (12) :1623-1629
[47]   Mineralocorticoid receptor knockout mice:: Lessons on Na+ metabolism [J].
Berger, S ;
Bleich, M ;
Schmid, W ;
Greger, R ;
Schütz, G .
KIDNEY INTERNATIONAL, 2000, 57 (04) :1295-1298
[48]  
BERNSTEIN KE, 1989, J BIOL CHEM, V264, P11945
[49]  
BHASKAR RM, 1984, PEPTIDES, V5, P291
[50]  
BICKERTON R, 1961, P SOC EXP BIOL MED, V106, P834