Low-dose renin inhibitor and low-dose AT1-receptor blocker therapy ameliorate target-organ damage in rats harbouring human renin and angiotensinogen genes
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Dechend, Ralf
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Dechend, Ralf
Shagdarsuren, Erdenechimeg
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Shagdarsuren, Erdenechimeg
Gratze, Petra
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Gratze, Petra
Fiebeler, Anette
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Fiebeler, Anette
Pilz, Bernhard
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Pilz, Bernhard
Meiners, Silke
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Meiners, Silke
Derer, Wolfgang
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Derer, Wolfgang
Feldman, David L.
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Feldman, David L.
Webb, Randy
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Webb, Randy
Muller, Dominik N.
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机构:Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
Muller, Dominik N.
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[1] Univ Med Berlin, Franz Volhard Clin, HELIOS Klinikum, Berlin, Germany
We studied the effects of extremely low-dose human renin inhibition (aliskiren) with low angiotensin 11 receptor blockade (losartan) in a novel double-transgenic rat model harbouring both human renin and angiotensinogen genes. We found that low-dose aliskiren and low-dose losartan effectively reduced mortality and target-organ damage with minimal, non-significant, effects on blood pressure (BP). Our data suggest that renin-angiotensin system (RAS) inhibition ameliorates target-organ damage in an Ang II-driven model of hypertension. Direct renin inhibition is equally efficacious in this regard. Our study does not fully answer the question of BP-lowering versus RAS inhibition. This question is important and was at least partially addressed with our low-dose model.