Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway

The current study was designed to determine the curative potential of astragalin (AST) against polystyrene microplastics (PS-MPs) induced hepatic toxicity in rats. PS-MPs exposure decreased the expression of Nrf-2 and anti-oxidant enzymes, while increasing Keap-1 expression. The activities of glutat...

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Main Authors: Ali Hamza, Muhammad Umar Ijaz, Nazia Ehsan, Hammad Ahmad Khan, Saad Alkahtani, Usman Atique
Format: Article
Language:English
Published: Elsevier 2023-09-01
Series:Journal of Functional Foods
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1756464623003717
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author Ali Hamza
Muhammad Umar Ijaz
Nazia Ehsan
Hammad Ahmad Khan
Saad Alkahtani
Usman Atique
author_facet Ali Hamza
Muhammad Umar Ijaz
Nazia Ehsan
Hammad Ahmad Khan
Saad Alkahtani
Usman Atique
author_sort Ali Hamza
collection DOAJ
description The current study was designed to determine the curative potential of astragalin (AST) against polystyrene microplastics (PS-MPs) induced hepatic toxicity in rats. PS-MPs exposure decreased the expression of Nrf-2 and anti-oxidant enzymes, while increasing Keap-1 expression. The activities of glutathione-S-transferase, catalase, glutathione, glutathione peroxidase, superoxide dismutase, glutathione reductase and heme oxygenase-1 were decreased, besides the levels of malondialdehyde and reactive oxygen species were also increased following the exposure of PS-MPs. The intoxication of PS-MPs elevated aspartate aminotransferase, alanine transaminase, alkaline phosphatase levels, as well as cyclooxygenase-2 activity, interleukin-6, interleukin-1 beta, nuclear factor-kappa B and tumor necrosis factor-alpha levels were also escalated. Furthermore, Bcl-2 expression was down-regulated, while Bax and Caspase-3 expressions were upregulated following PS-MPs exposure. Histopathological assessment revealed substantial liver damages in PS-MPs treated rats. However, AST supplementation substantially recovered PS-MPs-induced damages and histological anomalies. Therefore, AST can be used as a curative agent to treat PS-MPs-prompted hepatotoxicity due to its anti-apoptotic, anti-inflammatory and anti-oxidant potentials.
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spelling doaj.art-743b26a15168471ba9bbeec6e64e13562023-09-11T04:16:57ZengElsevierJournal of Functional Foods1756-46462023-09-01108105771Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathwayAli Hamza0Muhammad Umar Ijaz1Nazia Ehsan2Hammad Ahmad Khan3Saad Alkahtani4Usman Atique5Department of Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad 38040, PakistanDepartment of Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad 38040, Pakistan; Corresponding author.Department of Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad 38040, PakistanDepartment of Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad 38040, PakistanDepartment of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi ArabiaCollege of Biological Systems, Chungnam National University, Daejeon 34134, South KoreaThe current study was designed to determine the curative potential of astragalin (AST) against polystyrene microplastics (PS-MPs) induced hepatic toxicity in rats. PS-MPs exposure decreased the expression of Nrf-2 and anti-oxidant enzymes, while increasing Keap-1 expression. The activities of glutathione-S-transferase, catalase, glutathione, glutathione peroxidase, superoxide dismutase, glutathione reductase and heme oxygenase-1 were decreased, besides the levels of malondialdehyde and reactive oxygen species were also increased following the exposure of PS-MPs. The intoxication of PS-MPs elevated aspartate aminotransferase, alanine transaminase, alkaline phosphatase levels, as well as cyclooxygenase-2 activity, interleukin-6, interleukin-1 beta, nuclear factor-kappa B and tumor necrosis factor-alpha levels were also escalated. Furthermore, Bcl-2 expression was down-regulated, while Bax and Caspase-3 expressions were upregulated following PS-MPs exposure. Histopathological assessment revealed substantial liver damages in PS-MPs treated rats. However, AST supplementation substantially recovered PS-MPs-induced damages and histological anomalies. Therefore, AST can be used as a curative agent to treat PS-MPs-prompted hepatotoxicity due to its anti-apoptotic, anti-inflammatory and anti-oxidant potentials.http://www.sciencedirect.com/science/article/pii/S1756464623003717Polystyrene microplasticsAstragalinHepatotoxicityInflammationApoptosis
spellingShingle Ali Hamza
Muhammad Umar Ijaz
Nazia Ehsan
Hammad Ahmad Khan
Saad Alkahtani
Usman Atique
Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway
Journal of Functional Foods
Polystyrene microplastics
Astragalin
Hepatotoxicity
Inflammation
Apoptosis
title Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway
title_full Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway
title_fullStr Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway
title_full_unstemmed Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway
title_short Hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating Nrf-2/Keap-1 pathway
title_sort hepatoprotective effects of astragalin against polystyrene microplastics induced hepatic damage in male albino rats by modulating nrf 2 keap 1 pathway
topic Polystyrene microplastics
Astragalin
Hepatotoxicity
Inflammation
Apoptosis
url http://www.sciencedirect.com/science/article/pii/S1756464623003717
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