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In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury
OBJECTIVE(S): Renal ischemia-reperfusion injury (IRI) as a severe condition of acute kidney injury (AKI) is the most common clinical problem with high mortality rates of 35-60% deaths in hospital. Mesenchymal stem cells (MSC) due to unique regenerative characteristics are ideal candidates for the tr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118091/ https://www.ncbi.nlm.nih.gov/pubmed/30186570 http://dx.doi.org/10.22038/IJBMS.2018.26829.6566 |
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author | Havakhah, Shahrzad Sankian, Mojtaba Kazemzadeh, Gholam Hosein Sadri, Keyvan Bidkhori, Hamid Reza Naderi-Meshkin, Hojjat Ebrahimzadeh Bideskan, Alireza Niazmand, Saeed Bahrami, Ahmad Reza Khajavi Rad, Abolfazl |
author_facet | Havakhah, Shahrzad Sankian, Mojtaba Kazemzadeh, Gholam Hosein Sadri, Keyvan Bidkhori, Hamid Reza Naderi-Meshkin, Hojjat Ebrahimzadeh Bideskan, Alireza Niazmand, Saeed Bahrami, Ahmad Reza Khajavi Rad, Abolfazl |
author_sort | Havakhah, Shahrzad |
collection | PubMed |
description | OBJECTIVE(S): Renal ischemia-reperfusion injury (IRI) as a severe condition of acute kidney injury (AKI) is the most common clinical problem with high mortality rates of 35-60% deaths in hospital. Mesenchymal stem cells (MSC) due to unique regenerative characteristics are ideal candidates for the treatment of the ischemic injuries. This work is focused on the administration of MSC to IRI-induced AKI Wistar rats and evaluating their significance in AKI treatment. MATERIAL AND METHODS: Animals underwent surgical procedure and AKI was induced by 40 min bilateral renal pedicle clamping. Immediately after reperfusion, 2×106 rat bone marrow derived MSCs were injected via intra-parenchymal or intra-aortic route. RESULTS: Animals subjected to AKI after days 1 and 3 showed significant increase in the serum creatinine and blood urea nitrogen (BUN) concentration along with a declined glomerular filtration rate (GFR) when compared with non-ischemic animals. On the other hand, treated animals showed a significant enhanced regeneration as compared to ischemic animals in both administration route groups. CONCLUSION: According to the results concluded from the renoprotective effects of MSC in IRI/AKI, MSCs could be considered as promising therapeutic approach for AKI in clinical applications. |
format | Online Article Text |
id | pubmed-6118091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-61180912018-09-05 In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury Havakhah, Shahrzad Sankian, Mojtaba Kazemzadeh, Gholam Hosein Sadri, Keyvan Bidkhori, Hamid Reza Naderi-Meshkin, Hojjat Ebrahimzadeh Bideskan, Alireza Niazmand, Saeed Bahrami, Ahmad Reza Khajavi Rad, Abolfazl Iran J Basic Med Sci Original Article OBJECTIVE(S): Renal ischemia-reperfusion injury (IRI) as a severe condition of acute kidney injury (AKI) is the most common clinical problem with high mortality rates of 35-60% deaths in hospital. Mesenchymal stem cells (MSC) due to unique regenerative characteristics are ideal candidates for the treatment of the ischemic injuries. This work is focused on the administration of MSC to IRI-induced AKI Wistar rats and evaluating their significance in AKI treatment. MATERIAL AND METHODS: Animals underwent surgical procedure and AKI was induced by 40 min bilateral renal pedicle clamping. Immediately after reperfusion, 2×106 rat bone marrow derived MSCs were injected via intra-parenchymal or intra-aortic route. RESULTS: Animals subjected to AKI after days 1 and 3 showed significant increase in the serum creatinine and blood urea nitrogen (BUN) concentration along with a declined glomerular filtration rate (GFR) when compared with non-ischemic animals. On the other hand, treated animals showed a significant enhanced regeneration as compared to ischemic animals in both administration route groups. CONCLUSION: According to the results concluded from the renoprotective effects of MSC in IRI/AKI, MSCs could be considered as promising therapeutic approach for AKI in clinical applications. Mashhad University of Medical Sciences 2018-08 /pmc/articles/PMC6118091/ /pubmed/30186570 http://dx.doi.org/10.22038/IJBMS.2018.26829.6566 Text en © Iranian Journal of Basic Medical Sciences 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 Havakhah, Shahrzad Sankian, Mojtaba Kazemzadeh, Gholam Hosein Sadri, Keyvan Bidkhori, Hamid Reza Naderi-Meshkin, Hojjat Ebrahimzadeh Bideskan, Alireza Niazmand, Saeed Bahrami, Ahmad Reza Khajavi Rad, Abolfazl In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
title |
In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
title_full |
In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
title_fullStr |
In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
title_full_unstemmed |
In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
title_short |
In vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
title_sort | in vivo effects of allogeneic mesenchymal stem cells in a rat model of acute ischemic kidney injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118091/ https://www.ncbi.nlm.nih.gov/pubmed/30186570 http://dx.doi.org/10.22038/IJBMS.2018.26829.6566 |
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