Renin and Angiotensin II Receptor Gene Expression in Kidneys of Renal Hypertensive Rats

Author:

Haefliger Jacques-Antoine1,Bergonzelli Gabriela1,Waeber Gérard1,Aubert Jean-François1,Nussberger Jürg1,Gavras Haralambos1,Nicod Pascal1,Waeber Bernard1

Affiliation:

1. From the Department of Internal Medicine B (J.-A.H., G.B., G.W., P.N.) Centre Hospitalier Universitaire Vaudois, the Division of Hypertension (J.-F.A., J.N., B.W.), Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland, and the Hypertension Section (H.G.), Boston University Medical Center, Boston, Mass.

Abstract

Abstract The aim of this investigation was to examine the interrelation between renal mRNA levels of renin and angiotensin II receptor type 1 (AT 1 ) in a renin-dependent form of experimental hypertension. Rats were studied 4 weeks after unilateral renal artery clipping. Mean blood pressure and plasma renin activity were significantly higher in the hypertensive rats (n=10 206±8 mm Hg and 72.4±20.9 ng · mL −1 · h −1 , respectively) than in sham-operated controls (n=10, 136±3 mm Hg and 3.3±0.5 ng · mL −1 · h −1 , respectively). Northern blot analysis of polyA + RNA obtained from the kidneys of renal hypertensive rats showed increased levels of renin mRNA in the clipped kidney, whereas a decrease was observed in the unclipped kidney. Plasma renin activity was directly correlated with renin mRNA expression of the poststenotic kidney ( r =.94, P <.01). AT 1 mRNA expression was lower in both kidneys of the hypertensive rats. This downregulation was specific for the AT 1A subtype since the renal expression of the AT 1B subtype remained normal in hypertensive rats. The downregulation of the renal AT 1A receptor may be due to high circulating angiotensin II levels. This is supported by the significant inverse correlation ( r =−.71, P <.01) between plasma renin activity and AT 1A mRNA expression measured in the clipped kidney of the hypertensive rats.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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