Angiotensin II receptor antagonist delays renal damage and stroke in salt-loaded Dahl salt-sensitive rats

ObjectiveTo study the effects of blockade of the renin—angiotensin system upon the development of hypertension, end-organ damage and mortality in Dahl salt-sensitive (DSS) rats using an angiotensin II receptor antagonist, losartan.Design and methodsDSS rats (n = 186) were fed 8% NaCI from 6 to 16 we...

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Veröffentlicht in:Journal of hypertension 1992-09, Vol.10 (9), p.949-958
Hauptverfasser: von Lutterotti, Nicola, Camargo, Maria J.F, Campbell, Wallace G, Mueller, Franco B, Timmermans, Pieter B, Sealey, Jean E, Laragh, John H
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Sprache:eng
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Zusammenfassung:ObjectiveTo study the effects of blockade of the renin—angiotensin system upon the development of hypertension, end-organ damage and mortality in Dahl salt-sensitive (DSS) rats using an angiotensin II receptor antagonist, losartan.Design and methodsDSS rats (n = 186) were fed 8% NaCI from 6 to 16 weeks of age. One group received losartan whilst the control group was untreated. Changes in blood pressure and plasma renin activity (PRA), as well as renal and cerebrovascular damage and survival were assessed during the study.ResultsLosartan blunted the blood pressure rise only transiently. Salt loading suppressed PRA in both groups until week 4 and thereafter it rose more markedly in the treated group. With no treatment renal lesions were first detected at 2 weeks, and strokes at 6 weeks. However, losartan transiently decreased the incidence and delayed the progression of renal damage and cerebrovascular lesions (strokes) and increased survival. PRA correlated with renal damage and the incidence of strokes in both groups. Blood pressure only partially affected survival, but did not correlate with stroke incidence.ConclusionsThese results indicate that whereas the rise in blood pressure is dependent upon sodium loading, morbidity and mortality in salt-loaded DSS rats are associated with activation of the renin-angiotensin system and are only partially related to blood pressure.
ISSN:0263-6352
1473-5598
DOI:10.1097/00004872-199209000-00006