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Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study
OBJECTIVE(S): The aim of this study is to investigate the renoprotective effect of erythropoietin (EPO) on hypovolemic shock and ischemia/reperfusion (IR) injury on kidneys as end-organs in an experimentally-created ruptured abdominal aortic aneurysm (rAAA) model. MATERIALS AND METHODS: Thirty anest...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211356/ https://www.ncbi.nlm.nih.gov/pubmed/32405372 http://dx.doi.org/10.22038/IJBMS.2019.36215.8626 |
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author | Altun, Gokalp Cakiroglu, Yavuz Pulathan, Zerrin Yulug, Esin Mentese, Ahmet |
author_facet | Altun, Gokalp Cakiroglu, Yavuz Pulathan, Zerrin Yulug, Esin Mentese, Ahmet |
author_sort | Altun, Gokalp |
collection | PubMed |
description | OBJECTIVE(S): The aim of this study is to investigate the renoprotective effect of erythropoietin (EPO) on hypovolemic shock and ischemia/reperfusion (IR) injury on kidneys as end-organs in an experimentally-created ruptured abdominal aortic aneurysm (rAAA) model. MATERIALS AND METHODS: Thirty anesthetized Sprague-Dawley male rats were randomized to sham ((Sh n:6) (Sh+EPO n:6)) or shock and I/R groups ((S/IR n:9) (S/IR+EPO n:9)). Additional surgical procedure except aortic exploration was not performed on Sh and Sh+EPO groups. 60 min of shock, 60 min of ischemia, and 120 min of reperfusion were applied on S/IR and S/IR+EPO groups. In the S/IR and S/IR+EPO groups, hemorrhagic shock, lower torso ischemia, and reperfusion were created. At the end of the shock period, saline solutions were separately and equally administered to Sh and S/IR groups, whereas 2000 U/kg EPO was intraperitoneally administered to Sh+EPO and S/IR+EPO groups. At the end of the experimental study, some biochemical and histological parameters were studied in serum and kidney tissues. RESULTS: Biochemical parameters were all significantly increased in the S/IR group compared with the Sh group. These parameters were not statistically significantly different between S/IR+EPO and Sh+EPO groups. In histopathologic examination, EPO prevented high-grade injury. CONCLUSION: Our data indicate that EPO may have a renoprotective effect and reduce the systemic inflammatory response that resulted from shock and I/R in an experimental model of rAAA. |
format | Online Article Text |
id | pubmed-7211356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-72113562020-05-13 Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study Altun, Gokalp Cakiroglu, Yavuz Pulathan, Zerrin Yulug, Esin Mentese, Ahmet Iran J Basic Med Sci Original Article OBJECTIVE(S): The aim of this study is to investigate the renoprotective effect of erythropoietin (EPO) on hypovolemic shock and ischemia/reperfusion (IR) injury on kidneys as end-organs in an experimentally-created ruptured abdominal aortic aneurysm (rAAA) model. MATERIALS AND METHODS: Thirty anesthetized Sprague-Dawley male rats were randomized to sham ((Sh n:6) (Sh+EPO n:6)) or shock and I/R groups ((S/IR n:9) (S/IR+EPO n:9)). Additional surgical procedure except aortic exploration was not performed on Sh and Sh+EPO groups. 60 min of shock, 60 min of ischemia, and 120 min of reperfusion were applied on S/IR and S/IR+EPO groups. In the S/IR and S/IR+EPO groups, hemorrhagic shock, lower torso ischemia, and reperfusion were created. At the end of the shock period, saline solutions were separately and equally administered to Sh and S/IR groups, whereas 2000 U/kg EPO was intraperitoneally administered to Sh+EPO and S/IR+EPO groups. At the end of the experimental study, some biochemical and histological parameters were studied in serum and kidney tissues. RESULTS: Biochemical parameters were all significantly increased in the S/IR group compared with the Sh group. These parameters were not statistically significantly different between S/IR+EPO and Sh+EPO groups. In histopathologic examination, EPO prevented high-grade injury. CONCLUSION: Our data indicate that EPO may have a renoprotective effect and reduce the systemic inflammatory response that resulted from shock and I/R in an experimental model of rAAA. Mashhad University of Medical Sciences 2020-02 /pmc/articles/PMC7211356/ /pubmed/32405372 http://dx.doi.org/10.22038/IJBMS.2019.36215.8626 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Altun, Gokalp Cakiroglu, Yavuz Pulathan, Zerrin Yulug, Esin Mentese, Ahmet Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study |
title | Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study |
title_full | Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study |
title_fullStr | Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study |
title_full_unstemmed | Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study |
title_short | Renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: An animal study |
title_sort | renoprotective potential of exogen erythropoietin on experimental ruptured abdominal aortic aneurysm model: an animal study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211356/ https://www.ncbi.nlm.nih.gov/pubmed/32405372 http://dx.doi.org/10.22038/IJBMS.2019.36215.8626 |
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