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Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats

Ischemia-reperfusion injury (IRI) is a major contributor to acute and chronic kidney failure, heart failure, and ischemic stroke. This study aimed to investigate the therapeutic potential of Iberin, known for its anti-inflammatory, antioxidant, and antiapoptotic properties, in a rat model of renal I...

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Autores principales: Yahiya, Yahiya Ibrahim, Hadi, Najah Rayish, Abu Raghif, Ahmed, Qassam, Heider, AL Habooby, Noor Ghaffar Said
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478648/
https://www.ncbi.nlm.nih.gov/pubmed/37675177
http://dx.doi.org/10.25122/jml-2022-0281
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author Yahiya, Yahiya Ibrahim
Hadi, Najah Rayish
Abu Raghif, Ahmed
Qassam, Heider
AL Habooby, Noor Ghaffar Said
author_facet Yahiya, Yahiya Ibrahim
Hadi, Najah Rayish
Abu Raghif, Ahmed
Qassam, Heider
AL Habooby, Noor Ghaffar Said
author_sort Yahiya, Yahiya Ibrahim
collection PubMed
description Ischemia-reperfusion injury (IRI) is a major contributor to acute and chronic kidney failure, heart failure, and ischemic stroke. This study aimed to investigate the therapeutic potential of Iberin, known for its anti-inflammatory, antioxidant, and antiapoptotic properties, in a rat model of renal IRI. Twenty-four adult male rats were randomly divided into four groups: Group I (Sham group) underwent laparotomy without IRI induction; Group II (Control group) underwent laparotomy followed by renal artery clamping for 30 minutes to induce ischemia, followed by 2 hours of reperfusion; Group III (Iberin treatment group) received a pre-injection of Iberin (15 mg/kg) and underwent 30 minutes of ischemia followed by 2 hours of reperfusion; and Group IV (Vehicle-treated group) received the vehicle (ethanol) 1 hour prior to ischemia and reperfusion induction. Iberin was diluted with ethanol. Biomarkers associated with inflammation, oxidative stress, and apoptosis were measured using enzyme-linked immunosorbent assay. Iberin treatment significantly reduced levels of inflammatory cytokines interleukin-1β (IL-1β) and IL-6, Bcl-2-associated X protein (BAX), tumor necrosis factor α (TNF-α), nuclear factor kappa p56, high mobility group B1, and neutrophil gelatinase-associated lipocalin. Moreover, Iberin increased levels of heat shock protein and Bcl2 compared to the control and vehicle groups. Iberin treatment prolonged the ischemic tolerance of renal tissue, potentially preventing or delaying irreversible injuries. These findings highlight the potential of Iberin as a promising candidate for mitigating renal injury caused by ischemia-reperfusion, due to its ability to modulate inflammatory markers.
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spelling pubmed-104786482023-09-06 Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats Yahiya, Yahiya Ibrahim Hadi, Najah Rayish Abu Raghif, Ahmed Qassam, Heider AL Habooby, Noor Ghaffar Said J Med Life Original Article Ischemia-reperfusion injury (IRI) is a major contributor to acute and chronic kidney failure, heart failure, and ischemic stroke. This study aimed to investigate the therapeutic potential of Iberin, known for its anti-inflammatory, antioxidant, and antiapoptotic properties, in a rat model of renal IRI. Twenty-four adult male rats were randomly divided into four groups: Group I (Sham group) underwent laparotomy without IRI induction; Group II (Control group) underwent laparotomy followed by renal artery clamping for 30 minutes to induce ischemia, followed by 2 hours of reperfusion; Group III (Iberin treatment group) received a pre-injection of Iberin (15 mg/kg) and underwent 30 minutes of ischemia followed by 2 hours of reperfusion; and Group IV (Vehicle-treated group) received the vehicle (ethanol) 1 hour prior to ischemia and reperfusion induction. Iberin was diluted with ethanol. Biomarkers associated with inflammation, oxidative stress, and apoptosis were measured using enzyme-linked immunosorbent assay. Iberin treatment significantly reduced levels of inflammatory cytokines interleukin-1β (IL-1β) and IL-6, Bcl-2-associated X protein (BAX), tumor necrosis factor α (TNF-α), nuclear factor kappa p56, high mobility group B1, and neutrophil gelatinase-associated lipocalin. Moreover, Iberin increased levels of heat shock protein and Bcl2 compared to the control and vehicle groups. Iberin treatment prolonged the ischemic tolerance of renal tissue, potentially preventing or delaying irreversible injuries. These findings highlight the potential of Iberin as a promising candidate for mitigating renal injury caused by ischemia-reperfusion, due to its ability to modulate inflammatory markers. Carol Davila University Press 2023-06 /pmc/articles/PMC10478648/ /pubmed/37675177 http://dx.doi.org/10.25122/jml-2022-0281 Text en ©2023 JOURNAL of MEDICINE and LIFE https://creativecommons.org/licenses/by/3.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Original Article
Yahiya, Yahiya Ibrahim
Hadi, Najah Rayish
Abu Raghif, Ahmed
Qassam, Heider
AL Habooby, Noor Ghaffar Said
Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
title Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
title_full Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
title_fullStr Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
title_full_unstemmed Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
title_short Role of Iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
title_sort role of iberin as an anti-apoptotic agent on renal ischemia-reperfusion injury in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478648/
https://www.ncbi.nlm.nih.gov/pubmed/37675177
http://dx.doi.org/10.25122/jml-2022-0281
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