Low-dose renin inhibitor and low-dose AT(1)-receptor blocker therapy ameliorate target-organ damage in rats harbouring human renin and angiotensinogen genes

J Renin Angiotensin Aldosterone Syst. 2007 Jun;8(2):81-4. doi: 10.3317/jraas.2007.008.

Abstract

We studied the effects of extremely low-dose human renin inhibition (aliskiren) with low angiotensin II 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / pharmacology*
  • Angiotensinogen / drug effects
  • Angiotensinogen / genetics*
  • Animals
  • Animals, Genetically Modified
  • Antihypertensive Agents / pharmacology*
  • Fumarates / pharmacology*
  • Humans
  • Hypertension / drug therapy
  • Hypertension / genetics*
  • Rats
  • Receptor, Angiotensin, Type 1 / drug effects
  • Receptor, Angiotensin, Type 1 / physiology*
  • Renin / drug effects
  • Renin / genetics*
  • Renin-Angiotensin System / drug effects
  • Renin-Angiotensin System / physiology

Substances

  • Amides
  • Antihypertensive Agents
  • Fumarates
  • Receptor, Angiotensin, Type 1
  • Angiotensinogen
  • aliskiren
  • Renin