The effects of Mas receptor antagonist (A779) and renal perfusion pressure on serum nitrite concentration in male and female rats when angiotensin II receptors 1 & 2 were blocked

(2015) The effects of Mas receptor antagonist (A779) and renal perfusion pressure on serum nitrite concentration in male and female rats when angiotensin II receptors 1 & 2 were blocked. Physiology and Pharmacology. 437-+. ISSN 2476-5236

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Abstract

Introduction: Renin angiotensin system has an important role in blood pressure and renal functions. Active angiotensin-converting enzyme 2 converts angiotensin I into angiotensin-(1-7) which is a vasodilator hormone and interacts with nitric oxide changes as well as other angiotensin II receptors. In this study we evaluated the role of Mas receptor antagonist (A779) and renal perfusion pressure (RPP) on serum nitric oxide metabolite (nitrite) concentration when angiotensin II receptors (AT1R & AT2R) were blocked. Methods: After angiotensin II receptors blockage in anesthetized male and female rats, RPP was maintained at two levels 80 & 100 mmHg by occluder around aorta above the renal arteries, and the effects of placebo and A779 on concentration of serum nitrite level were studied. Results: The results showed that when angiotensin II receptors were blocked, the serum level of nitrite in both sexes, was not dependent on angiotensin-(1-7) receptor and did not change statistically, but by increasing renal perfusion pressure and in the presence of angiotensin-(1-7) receptor the serum level of nitrite increased significantly (p<0.05) in male rats but not in female rats. Conclusion: Using angiotensin II receptors blockades and by increase of RPP, the serum level of nitrite is sex-related. This study showed the importance of Mas receptor in male sex when AT1R & AT2R were blocked.

Item Type: Article
Keywords: angiotensin-(1-7) mas receptor angiotensin ii receptors nitrite spontaneously hypertensive-rats renin-angiotensin converting enzyme-2 in-vivo oxide system endothelium bradykinin synthase gender
Page Range: 437-+
Journal or Publication Title: Physiology and Pharmacology
Journal Index: ISI
Volume: 18
Number: 4
ISSN: 2476-5236
Depositing User: مهندس مهدی شریفی
URI: http://eprints.mui.ac.ir/id/eprint/4474

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