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Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference
Background: Renal ischemia/reperfusion (I/R) injury may be related to activity of reninangiotensin system (RAS), which is gender-related. In this study, it was attempted to compare the effect of angiotensin II (Ang II) receptor type 1 (AT1R) blockade; losartan in I/R injury in male and female rats....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nickan Research Institute
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040000/ https://www.ncbi.nlm.nih.gov/pubmed/27689110 http://dx.doi.org/10.15171/jrip.2016.29 |
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author | Moslemi, Fatemeh Taheri, Pegah Azimipoor, Mahdis Ramtin, Sina Hashemianfar, Mostafa Momeni- Ashjerdi, Ali Eshraghi-Jazi, Fatemeh Talebi, Ardeshir Nasri, Hamid Nematbakhsh, Mehdi |
author_facet | Moslemi, Fatemeh Taheri, Pegah Azimipoor, Mahdis Ramtin, Sina Hashemianfar, Mostafa Momeni- Ashjerdi, Ali Eshraghi-Jazi, Fatemeh Talebi, Ardeshir Nasri, Hamid Nematbakhsh, Mehdi |
author_sort | Moslemi, Fatemeh |
collection | PubMed |
description | Background: Renal ischemia/reperfusion (I/R) injury may be related to activity of reninangiotensin system (RAS), which is gender-related. In this study, it was attempted to compare the effect of angiotensin II (Ang II) receptor type 1 (AT1R) blockade; losartan in I/R injury in male and female rats. Materials and Methods: Male and female Wistar rats were assigned as sham surgery, control I/R groups treated with vehicle, and case I/R groups treated with losartan (30 mg/kg). Vehicle and losartan were given 2 hours before bilateral kidney ischemia induced by clamping renal arteries for 45 minutes followed by 24 hours of renal reperfusion. Results: The I/R injury significantly increased the serum levels of blood urea nitrogen (BUN) and creatinine (Cr), and kidney tissue damage score in both genders. However, losartan decreased these values in female rats significantly (P < 0.05). This was not observed in male rats. Conclusion: Losartan protects the kidney from I/R injury in female but not in male rats possibly because of gender-related difference of RAS. |
format | Online Article Text |
id | pubmed-5040000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nickan Research Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-50400002016-09-29 Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference Moslemi, Fatemeh Taheri, Pegah Azimipoor, Mahdis Ramtin, Sina Hashemianfar, Mostafa Momeni- Ashjerdi, Ali Eshraghi-Jazi, Fatemeh Talebi, Ardeshir Nasri, Hamid Nematbakhsh, Mehdi J Renal Inj Prev Short Communication Background: Renal ischemia/reperfusion (I/R) injury may be related to activity of reninangiotensin system (RAS), which is gender-related. In this study, it was attempted to compare the effect of angiotensin II (Ang II) receptor type 1 (AT1R) blockade; losartan in I/R injury in male and female rats. Materials and Methods: Male and female Wistar rats were assigned as sham surgery, control I/R groups treated with vehicle, and case I/R groups treated with losartan (30 mg/kg). Vehicle and losartan were given 2 hours before bilateral kidney ischemia induced by clamping renal arteries for 45 minutes followed by 24 hours of renal reperfusion. Results: The I/R injury significantly increased the serum levels of blood urea nitrogen (BUN) and creatinine (Cr), and kidney tissue damage score in both genders. However, losartan decreased these values in female rats significantly (P < 0.05). This was not observed in male rats. Conclusion: Losartan protects the kidney from I/R injury in female but not in male rats possibly because of gender-related difference of RAS. Nickan Research Institute 2016-07-28 /pmc/articles/PMC5040000/ /pubmed/27689110 http://dx.doi.org/10.15171/jrip.2016.29 Text en Copyright © 2016 The Author(s); Published by Nickan Research Institute http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Moslemi, Fatemeh Taheri, Pegah Azimipoor, Mahdis Ramtin, Sina Hashemianfar, Mostafa Momeni- Ashjerdi, Ali Eshraghi-Jazi, Fatemeh Talebi, Ardeshir Nasri, Hamid Nematbakhsh, Mehdi Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
title | Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
title_full | Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
title_fullStr | Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
title_full_unstemmed | Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
title_short | Effect of angiotensin II type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
title_sort | effect of angiotensin ii type 1 receptor blockade on kidney ischemia/reperfusion; a gender-related difference |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040000/ https://www.ncbi.nlm.nih.gov/pubmed/27689110 http://dx.doi.org/10.15171/jrip.2016.29 |
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