New insights into the renoprotective actions of the renin inhibitor aliskiren in experimental renal disease

被引:26
作者
Feldman, David L. [1 ,2 ]
机构
[1] Novartis Inst BioMed Res, Cardiovasc & Metab Dis Area, E Hanover, NJ 07936 USA
[2] Novartis Pharmaceut, E Hanover, NJ 07936 USA
关键词
aliskiren; kidney; mechanism; nephropathy; renin; GLOMERULAR EPITHELIAL-CELLS; RAT MESANGIAL CELLS; ANGIOTENSIN-CONVERTING ENZYME; ACTIVATED PROTEIN-KINASE; MESSENGER-RNA EXPRESSION; HANDLE-REGION PEPTIDE; IN-SITU HYBRIDIZATION; SMOOTH-MUSCLE-CELLS; DIABETIC-NEPHROPATHY; BLOOD-PRESSURE;
D O I
10.1038/hr.2010.19
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The renin-angiotensin-aldosterone system (RAAS) has a central function in the regulation of blood pressure. Aliskiren, the first direct renin inhibitor to be approved for the treatment of hypertension, blocks the RAAS at its point of activation. As renin inhibition acts at the top of the RAAS cascade, this mechanism has been proposed to offer advantages over existing modes of RAAS blockade. The RAAS is also considered to be a major factor in the pathogenesis of many renal diseases, especially diabetic nephropathy (DN), the main cause of end-stage renal disease. Existing therapies to block the RAAS slow the progression of DN, but they do not halt the disease. Therefore, more effective modes of interventions are needed. Studies to determine the efficacy of aliskiren in human renal disease are in progress. This review summarizes in vivo studies in which the efficacy of aliskiren was tested in experimental models of renal disease, and presents in vitro studies that provide insights into the possible mechanisms by which aliskiren confers renoprotection in animals. These works are discussed in the framework of the intrarenal RAAS and suggest that aliskiren may act by unique renoprotective mechanisms. Hypertension Research (2010) 33, 279-287; doi:10.1038/hr.2010.19; published online 5 March 2010
引用
收藏
页码:279 / 287
页数:9
相关论文
共 132 条
[1]   Angiotensin II activation of the JAK/STAT pathway in mesangial cells is altered by high glucose [J].
Amiri, F ;
Shaw, S ;
Wang, XD ;
Tang, J ;
Waller, JL ;
Eaton, DC ;
Marrero, MB .
KIDNEY INTERNATIONAL, 2002, 61 (05) :1605-1616
[2]   RENAL RENIN-ANGIOTENSIN SYSTEM IN DIABETES - FUNCTIONAL, IMMUNOHISTOCHEMICAL, AND MOLECULAR BIOLOGICAL CORRELATIONS [J].
ANDERSON, S ;
JUNG, FF ;
INGELFINGER, JR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (04) :F477-F486
[3]   Characterization of renin mRNA expression and enzyme activity in rat and mouse mesangial cells [J].
Andrade, AQ ;
Casarini, DE ;
Schor, N ;
Boim, MA .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2002, 35 (01) :17-24
[4]   Purification and characterization of angiotensin I-converting enzymes from mesangial cells in culture [J].
Andrade, MCC ;
Quinto, BMR ;
Carmona, AK ;
Ribas, OS ;
Boim, MA ;
Schor, N ;
Casarini, DE .
JOURNAL OF HYPERTENSION, 1998, 16 (12) :2063-2074
[5]  
Ardaillou R, 1999, J AM SOC NEPHROL, V10, pS40
[6]   NITRIC-OXIDE IN THE KIDNEY - SYNTHESIS, LOCALIZATION, AND FUNCTION [J].
BACHMANN, S ;
MUNDEL, P .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1994, 24 (01) :112-129
[7]   Aliskiren-binding increases the half life of renin and prorenin in rat aortic vascular smooth muscle cells [J].
Batenburg, Wendy W. ;
de Bruin, Rene J. A. ;
van Gool, Jeanette M. G. ;
Mueller, Dominik N. ;
Bader, Michael ;
Nguyen, Genevieve ;
Danser, A. H. Jan .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (06) :1151-1157
[8]   Prorenin is the endogenous agonist of the (pro)renin receptor. Binding kinetics of renin and prorenin in rat vascular smooth muscle cells overexpressing the human (pro)renin receptor [J].
Batenburg, Wendy W. ;
Krop, Manne ;
Garrelds, Ingrid M. ;
de Vries, Rene ;
de Bruin, Rene J. A. ;
Burckle, Celine A. ;
Muller, Dominik N. ;
Bader, Michael ;
Nguyen, Genevieve ;
Danser, A. H. Jan .
JOURNAL OF HYPERTENSION, 2007, 25 (12) :2441-2453
[9]  
Becker BN, 1998, EXP NEPHROL, V6, P57
[10]   PROXIMAL TUBULAR SECRETION OF ANGIOTENSIN-II IN RATS [J].
BRAAM, B ;
MITCHELL, KD ;
FOX, J ;
NAVAR, LG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :F891-F898