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Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats

Background: Acute kidney injury (AKI), also known as acute renal failure (ARF), has received considerable critical attention in recent years. Gentamicin (GM) is an antibiotic whose prolonged use results in AKI with a high mortality rate. Methods: Fifty adult female albino rats weighing 150–200 g wer...

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Autores principales: Abu Almaaty, Ali H., Elmasry, Reham A., Farrag, Mayada S., Althobaiti, Fayez, Aldhahrani, Adil, Fayad, Eman, Hussain, Mona A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417307/
https://www.ncbi.nlm.nih.gov/pubmed/34490290
http://dx.doi.org/10.3389/fmed.2021.689691
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author Abu Almaaty, Ali H.
Elmasry, Reham A.
Farrag, Mayada S.
Althobaiti, Fayez
Aldhahrani, Adil
Fayad, Eman
Hussain, Mona A.
author_facet Abu Almaaty, Ali H.
Elmasry, Reham A.
Farrag, Mayada S.
Althobaiti, Fayez
Aldhahrani, Adil
Fayad, Eman
Hussain, Mona A.
author_sort Abu Almaaty, Ali H.
collection PubMed
description Background: Acute kidney injury (AKI), also known as acute renal failure (ARF), has received considerable critical attention in recent years. Gentamicin (GM) is an antibiotic whose prolonged use results in AKI with a high mortality rate. Methods: Fifty adult female albino rats weighing 150–200 g were used. The animals were divided into five groups: the first group was the normal healthy control one, the second group received only 1 × 10(6) HUCB mononuclear cells (MNCs)/rat by intravenous (iv) injection, the third diseased group was given GM 100 mg/kg for 10 consecutive days by intraperitoneal injections, the fourth preventive group received 1 × 10(6) HUCB MNCs/rat by iv injection 24 h before gentamicin treatment, and the fifth treated group received 1 × 10(6) HUCB MNCs/rat by iv injection 24 h after gentamicin treatment. After 1 week of treatment, blood samples were collected, and kidneys were removed for histopathological examination. Results: Rats treated with HUCB MNCs in the treated group had a significant decrease in renal damage, low levels of biomarkers for nephrotoxicities such as serum creatinine and blood urea nitrogen, and low chromosomal aberrations compared to the diseased third group. The gene expression of KIM-1 and NGAL was decreased in response to HUCB treatment. Conclusions: HUCB MNCs have a curative effect against AKI and gentamicin-induced genotoxicity owing to their regenerative property.
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spelling pubmed-84173072021-09-05 Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats Abu Almaaty, Ali H. Elmasry, Reham A. Farrag, Mayada S. Althobaiti, Fayez Aldhahrani, Adil Fayad, Eman Hussain, Mona A. Front Med (Lausanne) Medicine Background: Acute kidney injury (AKI), also known as acute renal failure (ARF), has received considerable critical attention in recent years. Gentamicin (GM) is an antibiotic whose prolonged use results in AKI with a high mortality rate. Methods: Fifty adult female albino rats weighing 150–200 g were used. The animals were divided into five groups: the first group was the normal healthy control one, the second group received only 1 × 10(6) HUCB mononuclear cells (MNCs)/rat by intravenous (iv) injection, the third diseased group was given GM 100 mg/kg for 10 consecutive days by intraperitoneal injections, the fourth preventive group received 1 × 10(6) HUCB MNCs/rat by iv injection 24 h before gentamicin treatment, and the fifth treated group received 1 × 10(6) HUCB MNCs/rat by iv injection 24 h after gentamicin treatment. After 1 week of treatment, blood samples were collected, and kidneys were removed for histopathological examination. Results: Rats treated with HUCB MNCs in the treated group had a significant decrease in renal damage, low levels of biomarkers for nephrotoxicities such as serum creatinine and blood urea nitrogen, and low chromosomal aberrations compared to the diseased third group. The gene expression of KIM-1 and NGAL was decreased in response to HUCB treatment. Conclusions: HUCB MNCs have a curative effect against AKI and gentamicin-induced genotoxicity owing to their regenerative property. Frontiers Media S.A. 2021-08-19 /pmc/articles/PMC8417307/ /pubmed/34490290 http://dx.doi.org/10.3389/fmed.2021.689691 Text en Copyright © 2021 Abu Almaaty, Elmasry, Farrag, Althobaiti, Aldhahrani, Fayad and Hussain. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Abu Almaaty, Ali H.
Elmasry, Reham A.
Farrag, Mayada S.
Althobaiti, Fayez
Aldhahrani, Adil
Fayad, Eman
Hussain, Mona A.
Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats
title Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats
title_full Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats
title_fullStr Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats
title_full_unstemmed Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats
title_short Impact of Human Umbilical Cord Blood Mononuclear Cells on Gentamicin-Induced Renal Injury and Genotoxicity in Rats
title_sort impact of human umbilical cord blood mononuclear cells on gentamicin-induced renal injury and genotoxicity in rats
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417307/
https://www.ncbi.nlm.nih.gov/pubmed/34490290
http://dx.doi.org/10.3389/fmed.2021.689691
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