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Similar renoprotection after renin-angiotensin-dependent and -independent antihypertensive therapy in 5/6-nephrectomized Ren-2 transgenic rats: are there blood pressure-independent effects?
- Source :
-
Clinical and experimental pharmacology & physiology [Clin Exp Pharmacol Physiol] 2010 Dec; Vol. 37 (12), pp. 1159-69. - Publication Year :
- 2010
-
Abstract
- 1. Hypertension plays a critical role in the progression of chronic kidney disease (CKD) to end-stage renal disease (ESRD), but it has also been postulated that antihypertensive drugs that block the renin-angiotensin system (RAS) show class-specific renoprotective actions beyond their blood pressure (BP)-lowering effects. 2. Because this notion has recently been questioned, in the present study we compared the effects of a RAS-dependent antihypertensive therapy (a combination of trandolapril, an angiotensin-converting enzyme inhibitor (ACEI) and losartan, an angiotensin-II (AngII) receptor subtype 1A receptor antagonist) with a 'RAS-independent' antihypertensive therapy (a combination of labetalol, an alfa- and beta-adrenoreceptor antagonist with the diuretics, hydrochlorothiazide and furosemide) on the progression of CKD after 5/6 renal ablation (5/6 NX) in Ren-2 renin transgenic rats (TGR), a model of AngII-dependent hypertension. Normotensive transgene-negative Hannover Sprague-Dawley (HanSD) rats after 5/6 NX served as controls. 3. RAS-dependent and -independent antihypertensive therapies normalized BP and survival rate, and prevented the development of cardiac hypertrophy and glomerulosclerosis to the same degree in 5/6 NX HanSD rats and in 5/6 NX TGR. The present findings show that renoprotection, at least in rats after 5/6 NX, is predominantly BP-dependent. When equal lowering of BP was achieved, leading to normotension, cardio- and renoprotective effects were equivalent irrespective of the type of antihypertensive therapy. 4. These findings should be taken into consideration in attempts to develop new therapeutic approaches and strategies aimed to prevent the progression of CKD and to lower the incidence of ESRD.<br /> (© 2010 The Authors. Clinical and Experimental Pharmacology and Physiology © 2010 Blackwell Publishing Asia Pty Ltd.)
- Subjects :
- Aldosterone urine
Angiotensin II blood
Angiotensin II metabolism
Angiotensin II Type 1 Receptor Blockers pharmacology
Angiotensin-Converting Enzyme Inhibitors pharmacology
Animals
Cardiomegaly drug therapy
Cardiomegaly prevention & control
Creatinine blood
Creatinine metabolism
Creatinine urine
Diabetic Nephropathies drug therapy
Diabetic Nephropathies prevention & control
Diuretics pharmacology
Drug Therapy, Combination
Furosemide pharmacology
Hydrochlorothiazide pharmacology
Hypertension metabolism
Indoles pharmacology
Kidney Failure, Chronic drug therapy
Kidney Failure, Chronic metabolism
Labetalol pharmacology
Losartan pharmacology
Proteinuria blood
Proteinuria metabolism
Proteinuria urine
Rats
Rats, Sprague-Dawley
Rats, Transgenic
Renin metabolism
Antihypertensive Agents pharmacology
Blood Pressure drug effects
Hypertension drug therapy
Kidney Failure, Chronic prevention & control
Renin-Angiotensin System drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1440-1681
- Volume :
- 37
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Clinical and experimental pharmacology & physiology
- Publication Type :
- Academic Journal
- Accession number :
- 20880190
- Full Text :
- https://doi.org/10.1111/j.1440-1681.2010.05453.x