Key result
Sex differences influence renal Mas receptor expression and function across physiological and pathological states.
Why the study?
MasR expression and function interact with sex hormones and pathological conditions, warranting an evaluation of sex differences in renal MasR expression and functions.
This review highlights the complex interplay of sex hormones and pathological conditions on MasR expression and function in the renal system.
Sex differences in renal MasR warrant cautious interpretation; leaves open hypothesis-generating research on sex-specific RAS modulation.
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.
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Choopani et al. (2022) conducted a review in Renal system physiological and pathological conditions. Sex differences play a complex role in Mas receptor expression and functions within the renal system under both physiological and pathological conditions.
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