Angiotensin II receptor blockade limits glomerular injury in rats with reduced renal mass.
Open Access
- 1 September 1992
- journal article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 90 (3), 766-771
- https://doi.org/10.1172/jci115949
Abstract
The effects of angiotensin II (AII) blockade were compared with the effects of angiotensin converting enzyme inhibition in rats with reduced nephron number. Rats were subjected to five-sixths renal ablation and divided into four groups with similar values for blood pressure and serum creatinine after 2 wk. Group 1 then served as untreated controls, while group 2 received the AII receptor antagonist MK954 (which has previously been designated DuP753), group 3 received the converting enzyme inhibitor enalapril, and group 4 received a combination of reserpine, hydralazine, and hydrochlorothiazide. Micropuncture and morphologic studies were performed 10 wk later. Converting enzyme inhibition, AII receptor blockade, and the combination regimen were equally effective in reversing systemic hypertension (time-averaged systolic blood pressure: group 1, 185 +/- 5 mmHg; group 2, 125 +/- 2 mmHg; group 3, 127 +/- 2 mmHg; group 4, 117 +/- 4 mmHg). Micropuncture studies showed that glomerular transcapillary pressure was reduced significantly by converting enzyme inhibition and by AII blockade but not by the combination regimen (delta P: group 1, 49 +/- 1 mmHg; group 2, 42 +/- 1 mmHg; group 3, 40 +/- 2 mmHg, group 4, 47 +/- 1 mmHg). Reduction of systemic blood pressure was associated with the development of markedly less proteinuria and segmental glomerular sclerosis in rats receiving enalapril and MK954 but not in rats receiving the combination regimen (prevalence of glomerular sclerotic lesions: group 1, 41 +/- 4%; group 2, 9 +/- 1%; group 3, 9 +/- 1%; group 4, 33 +/- 6%). These results indicate that the effects of converting enzyme inhibition on remnant glomerular function and structure depend on reduction in AII activity and are not attributable simply to normalization of systemic blood pressure.This publication has 29 references indexed in Scilit:
- Impaired autoregulation of glomerular capillary hydrostatic pressure in the rat remnant nephron.Journal of Clinical Investigation, 1991
- DuP 753 is a specific antagonist for the angiotensin receptor.Hypertension, 1991
- Converting enzyme inhibition in kinin-deficient brown Norway rats.Hypertension, 1990
- Effect of dietary protein on the renin-angiotensin system in subtotally nephrectomized ratsKidney International, 1990
- Hypotensive action of DuP 753, an angiotensin II antagonist, in spontaneously hypertensive rats. Nonpeptide angiotensin II receptor antagonists: X.Hypertension, 1990
- Effect of converting enzyme inhibition on the course of adriamycin-induced nephropathyKidney International, 1989
- Kinin antagonist reverses converting enzyme inhibitor-stimulated vascular prostaglandin I2 synthesis.Hypertension, 1989
- Sodium regulation of angiotensinogen mRNA expression in rat kidney cortex and medulla.Journal of Clinical Investigation, 1986
- Contribution of the renin-angiotensin system to the control of intrarenal hemodynamicsKidney International, 1984
- RENIN SECRETION IN RENAL HYPERTENSIONThe Lancet, 1970