Pregnancy Enhances the Angiotensin (Ang)-(1–7) Vasodilator Response in Mesenteric Arteries and Increases the Renal Concentration and Urinary Excretion of Ang-(1–7)

Author:

Neves Liomar A. A.1,Williams Aleck F.1,Averill David B.1,Ferrario Carlos M.1,Walkup Michael P.2,Brosnihan K. Bridget1

Affiliation:

1. The Hypertension and Vascular Disease Center (L.A.A.N., A.F.W., D.B.A., C.M.F., K.B.B.), Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157-1932

2. Public Health Sciences (M.P.W.), Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157-1932

Abstract

Abstract The vasoactive effect of angiotensin (Ang)-(1–7) in mesenteric resistance arteries together with its plasma and kidney concentration and urinary excretion was assessed in pregnant and virgin rats. Mesenteric arteries (230–290 μm) were mounted in a pressurized myograph system and Ang-(1–7) concentration-dependent response curves (10−10–10−5m) were determined in arteries preconstricted with endothelin-1 (10−7m). The Ang-(1–7) response was investigated in vessels with and without pretreatment with the Ang-(1–7) antagonist [d-[Ala7]-Ang-(1–7)] (10−7m). Ang-(1–7) caused a significantly enhanced, concentration-dependent dilation of mesenteric vessels (EC50 = 2.7 nm) from pregnant compared with virgin female rats. d-[Ala7]-Ang-(1–7) eliminated the vasodilator effect of Ang-(1–7). There was no significant change in plasma concentration of Ang-(1–7) in pregnant animals. On the other hand, 24 h urinary excretion and kidney concentration of Ang-(1–7) were significantly higher in pregnant animals. The increased mesenteric dilation to Ang-(1–7) with enhanced kidney concentration and 24 h urinary excretion rate of Ang-(1–7) suggests an important role for this peptide in cardiovascular regulation during pregnancy.

Publisher

The Endocrine Society

Subject

Endocrinology

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