Sex Difference in MasR Expression and Functions in the Renal System

(2022) Sex Difference in MasR Expression and Functions in the Renal System. Journal of the Renin-Angiotensin-Aldosterone System. p. 10. ISSN 1470-3203

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Abstract

Renin-angiotensin system (RAS), as a critical system for controlling body fluid and hemostasis, contains peptides and receptors, including angiotensin 1-7 (Ang 1-7) and Mas receptor (MasR). Ang 1-7 implements its function via MasR. Ang II is another peptide in RAS that performs its actions via two Ang II type 1 and 2 receptors (AT1R and AT2R). The functions of AT2R and MasR are very similar, and both have a vasodilation effect, while AT1R has a vasoconstriction role. MasR affects many mechanisms in the brain, heart, blood vessels, kidney, lung, endocrine, reproductive, skeletal muscle, and liver and probably acts like a paracrine hormone in these organs. The effect of Ang 1-7 in the kidney is complex according to the hydroelectrolyte status, the renal sympathetic nervous system, and the activity level of the RAS. The MasR expression and function seem more complex than Ang II receptors and have interacted with Ang II receptors and many other factors, including sex hormones. Also, pathological conditions including hypertension, diabetes, and ischemia-reperfusion could change MasR expression and function. In this review, we consider the role of sex differences in MasR expression and functions in the renal system under physiological and pathological conditions.

Item Type: Article
Keywords: angiotensin-converting enzyme receptor antagonist a779 blood-flow response at(1) receptors nitric-oxide myocardial-infarction induced hypertension vascular-response genetic deletion oxidative stress Cardiovascular System & Cardiology
Page Range: p. 10
Journal or Publication Title: Journal of the Renin-Angiotensin-Aldosterone System
Journal Index: ISI
Volume: 2022
Identification Number: https://doi.org/10.1155/2022/1327839
ISSN: 1470-3203
Depositing User: خانم ناهید ضیائی
URI: http://eprints.mui.ac.ir/id/eprint/25507

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