Blood Pressure–Independent Cardiac Hypertrophy Induced by Locally Activated Renin-Angiotensin System

Author:

Mazzolai Lucia1,Nussberger Jürg1,Aubert Jean-François1,Brunner Dorette B.1,Gabbiani Giulio1,Brunner Hans R.1,Pedrazzini Thierry1

Affiliation:

1. From the Division of Hypertension and Vascular Medicine, University of Lausanne Medical School (L.M., J.N., J.-F.A., D.B.B., H.R.B., T.P.), and the Department of Pathology, University of Geneva Medical School (G.G.), Switzerland.

Abstract

Abstract —Cardiac hypertrophy is frequent in chronic hypertension. The renin-angiotensin system, via its effector angiotensin II (Ang II), regulates blood pressure and participates in sustaining hypertension. In addition, a growing body of evidence indicates that Ang II acts also as a growth factor. However, it is still a matter of debate whether the trophic effect of Ang II can trigger cardiac hypertrophy in the absence of elevated blood pressure. To address this question, transgenic mice overexpressing the rat angiotensinogen gene, specifically in the heart, were generated to increase the local activity of the renin-angiotensin system and therefore Ang II production. These mice develop myocardial hypertrophy without signs of fibrosis independently from the presence of hypertension, demonstrating that local Ang II production is important in mediating the hypertrophic response in vivo.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

Reference31 articles.

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