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Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts

Reports related to the effects of Echis coloratus venom (EcV) on the antioxidant capacity of human tissues is very scarce. The present study was undertaken to investigate the activities and gene expression levels of glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase...

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Autores principales: Al-Sheikh, Yazeed A., Ghneim, Hazem K., Aljaser, Feda S., Aboul-Soud, Mourad A.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488744/
https://www.ncbi.nlm.nih.gov/pubmed/28672988
http://dx.doi.org/10.3892/etm.2017.4522
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author Al-Sheikh, Yazeed A.
Ghneim, Hazem K.
Aljaser, Feda S.
Aboul-Soud, Mourad A.M.
author_facet Al-Sheikh, Yazeed A.
Ghneim, Hazem K.
Aljaser, Feda S.
Aboul-Soud, Mourad A.M.
author_sort Al-Sheikh, Yazeed A.
collection PubMed
description Reports related to the effects of Echis coloratus venom (EcV) on the antioxidant capacity of human tissues is very scarce. The present study was undertaken to investigate the activities and gene expression levels of glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase (GST), superoxide dismutase (SOD) and catalase (CAT), as well as the levels of reduced glutathione (GSH), oxidized glutathione (GSSG) and the generation rates of superoxide anions (SOA), hydrogen peroxide (H(2)O(2)) and lipid peroxides (LPO) in cultured human fibroblasts incubated with EcV, ascorbate (Asc) and EcV plus Asc at concentrations and incubation periods that maintained cell viability. Results indicated that the activities of all antioxidant enzymes and their corresponding transcripts underwent highly significant decreases and downregulation in EcV-treated cultures (0.5 µg/ml medium for 4 h) compared to venom-free controls (P<0.001). Additionally, there were concurrent equally significant increases in SOA, H(2)O(2) and LPO generation rates in the venom-incubated cultures compared to controls (P<0.001). Results also indicated very significant decreases and parallel equally significant increases in GSH and GSSG levels respectively in the envenomed cultures compared to controls (P<0.001) leading to a drastically lower GSH/GSSG ratio. However, further incubation of the EcV-treated cultures with Asc (400 µM for 12 h) restored the activities and levels of all investigated parameters including the expression levels of the antioxidant genes to control venom-free values. It is concluded that Asc acted to neutralize the increased reactive oxygen species generation, thus ameliorating the EcV-induced oxidative stress and alleviating the downregulation of antioxidant genes.
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spelling pubmed-54887442017-06-30 Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts Al-Sheikh, Yazeed A. Ghneim, Hazem K. Aljaser, Feda S. Aboul-Soud, Mourad A.M. Exp Ther Med Articles Reports related to the effects of Echis coloratus venom (EcV) on the antioxidant capacity of human tissues is very scarce. The present study was undertaken to investigate the activities and gene expression levels of glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase (GST), superoxide dismutase (SOD) and catalase (CAT), as well as the levels of reduced glutathione (GSH), oxidized glutathione (GSSG) and the generation rates of superoxide anions (SOA), hydrogen peroxide (H(2)O(2)) and lipid peroxides (LPO) in cultured human fibroblasts incubated with EcV, ascorbate (Asc) and EcV plus Asc at concentrations and incubation periods that maintained cell viability. Results indicated that the activities of all antioxidant enzymes and their corresponding transcripts underwent highly significant decreases and downregulation in EcV-treated cultures (0.5 µg/ml medium for 4 h) compared to venom-free controls (P<0.001). Additionally, there were concurrent equally significant increases in SOA, H(2)O(2) and LPO generation rates in the venom-incubated cultures compared to controls (P<0.001). Results also indicated very significant decreases and parallel equally significant increases in GSH and GSSG levels respectively in the envenomed cultures compared to controls (P<0.001) leading to a drastically lower GSH/GSSG ratio. However, further incubation of the EcV-treated cultures with Asc (400 µM for 12 h) restored the activities and levels of all investigated parameters including the expression levels of the antioxidant genes to control venom-free values. It is concluded that Asc acted to neutralize the increased reactive oxygen species generation, thus ameliorating the EcV-induced oxidative stress and alleviating the downregulation of antioxidant genes. D.A. Spandidos 2017-07 2017-05-30 /pmc/articles/PMC5488744/ /pubmed/28672988 http://dx.doi.org/10.3892/etm.2017.4522 Text en Copyright: © Al-Sheikh et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Al-Sheikh, Yazeed A.
Ghneim, Hazem K.
Aljaser, Feda S.
Aboul-Soud, Mourad A.M.
Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts
title Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts
title_full Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts
title_fullStr Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts
title_full_unstemmed Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts
title_short Ascorbate ameliorates Echis coloratus venom-induced oxidative stress in human fibroblasts
title_sort ascorbate ameliorates echis coloratus venom-induced oxidative stress in human fibroblasts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488744/
https://www.ncbi.nlm.nih.gov/pubmed/28672988
http://dx.doi.org/10.3892/etm.2017.4522
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