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Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension

BACKGROUND: The prevalence and severity of hypertension, as well as the activity of the systemic and local renin angiotensin systems (RASs), are gender related, with more symptoms in males than in females. However, the underlying mechanisms are not well understood. In this study, we investigated sex...

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Autores principales: Pezeshki, Zahra, Nematbakhsh, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914082/
https://www.ncbi.nlm.nih.gov/pubmed/33688433
http://dx.doi.org/10.1155/2021/8820646
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author Pezeshki, Zahra
Nematbakhsh, Mehdi
author_facet Pezeshki, Zahra
Nematbakhsh, Mehdi
author_sort Pezeshki, Zahra
collection PubMed
description BACKGROUND: The prevalence and severity of hypertension, as well as the activity of the systemic and local renin angiotensin systems (RASs), are gender related, with more symptoms in males than in females. However, the underlying mechanisms are not well understood. In this study, we investigated sex differences in renal vascular responses to angiotensin II (Ang II) administration with and without Ang II type 1 and Mas receptor (AT(1)R and MasR) antagonists (losartan and A779) in the 2K1C rat model of renovascular hypertension. METHODS: Male and female 2K1C rats were divided into 8 experimental groups (4 of each sex) treated with vehicle, losartan, A779, or A779+losartan. Responses of mean arterial pressure (MAP), renal blood flow (RBF), and renal vascular resistance (RVR) to Ang II were determined. RESULTS: In both sexes, the basal MAP, RBF, and RVR were not significantly different between the four groups during the control period. The Ang II administration decreased RBF and increased RVR in a dose-related manner in both sexes pretreated with vehicle or A779 (P(dose) < 0.0001), but in vehicle pretreated groups, RBF and RVR responses were different between male and female rats (P(group) < 0.05). AT(1)R blockade increased RBF and decreased RVR responses to Ang II, and no difference between the sexes was detected. Coblockades of AT(1)R and MasR receptors increased RBF response to Ang II significantly in males alone but not in females (P(group)=0.04). CONCLUSION: The impact of Ang II on RBF and RVR responses seems to be gender related with a greater effect on males, and this sex difference abolishes by Mas receptor blockade. However, the paradoxical role of dual losartan and A779 may provide the different receptor interaction in RAS between male and female rats.
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spelling pubmed-79140822021-03-08 Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension Pezeshki, Zahra Nematbakhsh, Mehdi Int J Hypertens Research Article BACKGROUND: The prevalence and severity of hypertension, as well as the activity of the systemic and local renin angiotensin systems (RASs), are gender related, with more symptoms in males than in females. However, the underlying mechanisms are not well understood. In this study, we investigated sex differences in renal vascular responses to angiotensin II (Ang II) administration with and without Ang II type 1 and Mas receptor (AT(1)R and MasR) antagonists (losartan and A779) in the 2K1C rat model of renovascular hypertension. METHODS: Male and female 2K1C rats were divided into 8 experimental groups (4 of each sex) treated with vehicle, losartan, A779, or A779+losartan. Responses of mean arterial pressure (MAP), renal blood flow (RBF), and renal vascular resistance (RVR) to Ang II were determined. RESULTS: In both sexes, the basal MAP, RBF, and RVR were not significantly different between the four groups during the control period. The Ang II administration decreased RBF and increased RVR in a dose-related manner in both sexes pretreated with vehicle or A779 (P(dose) < 0.0001), but in vehicle pretreated groups, RBF and RVR responses were different between male and female rats (P(group) < 0.05). AT(1)R blockade increased RBF and decreased RVR responses to Ang II, and no difference between the sexes was detected. Coblockades of AT(1)R and MasR receptors increased RBF response to Ang II significantly in males alone but not in females (P(group)=0.04). CONCLUSION: The impact of Ang II on RBF and RVR responses seems to be gender related with a greater effect on males, and this sex difference abolishes by Mas receptor blockade. However, the paradoxical role of dual losartan and A779 may provide the different receptor interaction in RAS between male and female rats. Hindawi 2021-02-20 /pmc/articles/PMC7914082/ /pubmed/33688433 http://dx.doi.org/10.1155/2021/8820646 Text en Copyright © 2021 Zahra Pezeshki and Mehdi Nematbakhsh. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pezeshki, Zahra
Nematbakhsh, Mehdi
Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension
title Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension
title_full Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension
title_fullStr Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension
title_full_unstemmed Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension
title_short Sex Differences in the Renal Vascular Responses of AT(1) and Mas Receptors in Two-Kidney-One-Clip Hypertension
title_sort sex differences in the renal vascular responses of at(1) and mas receptors in two-kidney-one-clip hypertension
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914082/
https://www.ncbi.nlm.nih.gov/pubmed/33688433
http://dx.doi.org/10.1155/2021/8820646
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