Chronic renal diseases: Renoprotective benefits of renin-angiotensin system inhibition

被引:209
作者
Remuzzi, G [1 ]
Ruggenenti, P [1 ]
Perico, N [1 ]
机构
[1] Mario Negri Inst Pharmacol Res, I-24125 Bergamo, Italy
关键词
D O I
10.7326/0003-4819-136-8-200204160-00010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Progression to renal parenchymal damage and end-stage renal disease, which seems to be largely independent of the initial insult, is the final common pathway for chronic, proteinuric nephropathies in animals and humans. The key event is enhanced glomerular capillary pressure; this impairs glomerular permeability to proteins and permits excessive amounts of proteins to reach the lumen of the proximal tubule. The secondary process of reabsorption of filtered proteins can contribute to renal interstitial injury by activating intracellular events, including upregulation of the genes encoding vasoactive and inflammatory mediators, Both interstitial inflammation and progression of disease can be controlled by such drugs as angiotensin-converting enzyme inhibitors, which strengthen the glomerular permeability barrier to proteins and thereby limit proteinuria and filtered protein-dependent inflammatory signals. Clinical data strongly suggest that remission can now be achieved in some patients with chronic renal disease. Because of the current lag time between starting treatment and remission, however, a substantial proportion of patients still progress to end-stage renal disease before renal function begins to stabilize. A multimodal approach that centers on reducing or removing all risk factors associated with the progression of renal disease may decrease the time to remission of the disease for most patients with proteinuric nephropathies.
引用
收藏
页码:604 / 615
页数:12
相关论文
共 87 条
[1]  
Abbate M, 1998, J AM SOC NEPHROL, V9, P1213
[2]  
Addis T., 1940, J AMER MED ASSOC, V55, P223
[3]   THERAPEUTIC ADVANTAGE OF CONVERTING ENZYME-INHIBITORS IN ARRESTING PROGRESSIVE RENAL-DISEASE ASSOCIATED WITH SYSTEMIC HYPERTENSION IN THE RAT [J].
ANDERSON, S ;
RENNKE, HG ;
BRENNER, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (06) :1993-2000
[4]   ADDITIVE EFFECTS OF COMBINED ANGIOTENSIN-CONVERTING ENZYME-INHIBITION AND ANGIOTENSIN-II ANTAGONISM ON BLOOD-PRESSURE AND RENIN RELEASE IN SODIUM-DEPLETED NORMOTENSIVES [J].
AZIZI, M ;
CHATELLIER, G ;
GUYENE, TT ;
MURIETAGEOFFROY, D ;
MENARD, J .
CIRCULATION, 1995, 92 (04) :825-834
[5]   Effects of an ACE inhibitor calcium antagonist combination on proteinuria in diabetic nephropathy [J].
Bakris, GL ;
Weir, MR ;
DeQuattro, V ;
McMahon, FG .
KIDNEY INTERNATIONAL, 1998, 54 (04) :1283-1289
[6]   Renoprotective effect of contemporary blocking of angiotensin II and endothelin-1 in rats with membranous nephropathy [J].
Benigni, A ;
Corna, D ;
Maffi, R ;
Benedetti, G ;
Zoja, C ;
Remuzzi, G .
KIDNEY INTERNATIONAL, 1998, 54 (02) :353-359
[7]   TUBULOINTERSTITIAL LESIONS MEDIATE RENAL DAMAGE IN ADRIAMYCIN GLOMERULOPATHY [J].
BERTANI, T ;
CUTILLO, F ;
ZOJA, C ;
BROGGINI, M ;
REMUZZI, G .
KIDNEY INTERNATIONAL, 1986, 30 (04) :488-496
[8]  
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[9]  
BRENNER BM, 1982, NEW ENGL J MED, V307, P652, DOI 10.1056/NEJM198209093071104
[10]   Predictors of the progression of renal insufficiency in patients with insulin-dependent diabetes and overt diabetic nephropathy [J].
Breyer, JA ;
Bain, RP ;
Evans, JK ;
Nahman, NS ;
Lewis, EJ ;
Cooper, M ;
McGill, J ;
Berl, T ;
Rohde, R ;
Hunsicker, LG ;
Lachin, J ;
Greenhouse, SW ;
Verme, DA ;
Turlington, TR ;
Burrows, PK ;
Wish, J ;
Sheehan, J ;
Pohl, M ;
Berl, T ;
Santiago, G ;
Hunsicker, L ;
Kern, EFO ;
Lemann, J ;
Blementhal, S ;
Bresnahan, BS ;
Hebert, L ;
Goldfarb, S ;
Kobrin, S ;
Rodby, R ;
Levey, A ;
McLaughlin, M ;
Williams, M ;
McGill, J ;
Whittler, F ;
Rutecki, G ;
Cattran, D ;
Lietz, S ;
Valaitis, D ;
Hano, J ;
Maxwell, D ;
Porush, J ;
Spitalewitz, S ;
Shapiro, K ;
Adler, S ;
Tolchin, N ;
Hoy, W ;
Bernstein, R ;
Svetkey, L ;
Sharon, Z ;
Rausenbaum, B .
KIDNEY INTERNATIONAL, 1996, 50 (05) :1651-1658