A lower ratio of AT1/AT2 receptors of angiotensin II is found in female than in male spontaneously hypertensive rats

Objective: Sexual dimorphism has been observed in arterial hypertension. Blood pressure levels are lower in female than in male spontaneously hypertensive rats (SHR). Angiotensin II (Ang II) plays a major role in the regulation of blood pressure. The aim of this study was to compare Ang IIvascular reactivity and AT(1) and AT(2) receptor gene expression in female and male SHR. Methods: SHR animals were divided into four groups: (I) mate, (II) female in physiological estrus, (III) ovariectomized and (IV) ovariectomized treated with estrogen. Arterial blood pressure, AT, and AT, mRNA expression were determined. Ang II responses in aorta and mesenteric vessels were also evaluated. Results: In female SHR. aorta and mesenteric microvessels were hyporeactive to Ang II in comparison to male SHR. In ovariectomized females. Ang II vasoconstriction was similar to that of males. Estrogen treatment abolished this difference. The mRNA expression for AT(1) was higher in aorta and mesenteric vessels from males than in females. In ovariectomized SHR, mRNA expression for AT(1) was comparable to that of mates. Treatment with estrogen reversed the over expression observed. Whereas AT(2) gene expression did not differ, a lower ratio AT(1)/AT(2), was found in female than in male vessels. A higher mRNA expression for AT, was observed in kidney from male than in female. Ovariectomy resulted in Up-regulation of this Subtype receptor. Treatment with estrogen reversed the overexpression. AT(2) gene expression was higher in kidney from female than male SHR. Ovariectomy reduced AT(2) gene expression and estrogen treatment reversed the alteration observed in kidney. Conclusion: There is sexual dimorphism in vascular reactivity and in receptor gene expression to Ang II in SHR. We conclude that estrogen modulates AT(1) and AT(2) receptor gene expression and that this might explain at least partially the lower blood pressure observed in female SHR. (C) 2004 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.