Sex Difference in MasR Expression and Functions in the Renal System
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 A...
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Veröffentlicht in: | Journal of the Renin-Angiotensin-Aldosterone System 2022-01, Vol.2022, p.1327839-1327839 |
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description | 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. |
doi_str_mv | 10.1155/2022/1327839 |
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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.</description><identifier>ISSN: 1470-3203</identifier><identifier>EISSN: 1752-8976</identifier><identifier>DOI: 10.1155/2022/1327839</identifier><language>eng</language><publisher>New York: Hindawi</publisher><subject>Endocrine system ; Gender differences ; Hormones ; Nephrology ; Pathophysiology ; Review</subject><ispartof>Journal of the Renin-Angiotensin-Aldosterone System, 2022-01, Vol.2022, p.1327839-1327839</ispartof><rights>Copyright © 2022 Samira Choopani and Mehdi Nematbakhsh.</rights><rights>Copyright Hindawi Limited Jan 2022</rights><rights>Copyright © 2022 Samira Choopani and Mehdi Nematbakhsh. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-77b2b0ca6cf818df50613dc37d13cc75f7d68b5b33971badfaecafc028ef6833</citedby><cites>FETCH-LOGICAL-c459t-77b2b0ca6cf818df50613dc37d13cc75f7d68b5b33971badfaecafc028ef6833</cites><orcidid>0000-0003-1063-0180 ; 0000-0002-9565-9187</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482541/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482541/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,313,314,727,780,784,792,885,27922,27924,27925,53791,53793</link.rule.ids></links><search><contributor>Olatunji, Lawrence Aderemi</contributor><creatorcontrib>Choopani, Samira</creatorcontrib><creatorcontrib>Nematbakhsh, Mehdi</creatorcontrib><title>Sex Difference in MasR Expression and Functions in the Renal System</title><title>Journal of the Renin-Angiotensin-Aldosterone System</title><description>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.</description><subject>Endocrine system</subject><subject>Gender differences</subject><subject>Hormones</subject><subject>Nephrology</subject><subject>Pathophysiology</subject><subject>Review</subject><issn>1470-3203</issn><issn>1752-8976</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>AFRWT</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp90V1LwzAUBuAiCn7e-QMK3ihal4-mSW8EmZsKijC9D2l64iJtOpNW3b-3o0NR0Ksk5OHlHN4oOsToHGPGRgQRMsKUcEHzjWgHc0YSkfNss7-nHCWUILod7YbwghAVaUp2ovEjfMRX1hjw4DTE1sX3KsziycfCQwi2cbFyZTztnG77R1iBdg7xDJyq4sdlaKHej7aMqgIcrM-96Gk6eRrfJHcP17fjy7tEpyxvE84LUiCtMm0EFqVhKMO01JSXmGrNmeFlJgpWUJpzXKjSKNDKaEQEmExQuhddDLGLrqih1OBaryq58LZWfikbZeXPH2fn8rl5k3kqCEtxH3C8DvDNawehlbUNGqpKOWi6IAnHPMuzVOQ9PfpFX5rO9yv3KqeCUM4x69XZoLRvQvBgvobBSK4akatG5LqRnp8MPKhn-A78w54Odm5dqd7t_8mfrM6Xfg</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Choopani, Samira</creator><creator>Nematbakhsh, Mehdi</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AFRWT</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1063-0180</orcidid><orcidid>https://orcid.org/0000-0002-9565-9187</orcidid></search><sort><creationdate>20220101</creationdate><title>Sex Difference in MasR Expression and Functions in the Renal System</title><author>Choopani, Samira ; 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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. 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subjects | Endocrine system Gender differences Hormones Nephrology Pathophysiology Review |
title | Sex Difference in MasR Expression and Functions in the Renal System |
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