Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters

Objective: Schwann cells are the main cells for myelination and regeneration of peripheral nerves. Idebenone is asynthetic antioxidant used to treat central nervous system diseases. The aim of the study is to determine whether idebenonecan protect Schwann cells and increase cell activity under condi...

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Main Authors: Sam Zarbakhsh, Parisa Hayat
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2024-03-01
Series:Cell Journal
Subjects:
Online Access:https://www.celljournal.org/article_710540_43b5d1b0e44c864dfae1d5d4f09fe32a.pdf
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author Sam Zarbakhsh
Parisa Hayat
author_facet Sam Zarbakhsh
Parisa Hayat
author_sort Sam Zarbakhsh
collection DOAJ
description Objective: Schwann cells are the main cells for myelination and regeneration of peripheral nerves. Idebenone is asynthetic antioxidant used to treat central nervous system diseases. The aim of the study is to determine whether idebenonecan protect Schwann cells and increase cell activity under conditions of oxidative stress caused by hydrogen peroxide(H2O2) in vitro.Materials and Methods: In this experimental study, Schwann cells were pre-treated with various concentrations ofidebenone and H2O2; after determining the appropriate doses, the cells were treated with 10 μM idebenone for 48hours and 1000 μM H2O2 for the last two hours. The malondialdehyde (MDA) level, and activity of superoxide dismutase(SOD), catalase (CAT), and glutathione peroxidase (GPx) were assessed by ELISA. Cell viability was assessed bythe MTT assay. Western blot analysis was conducted to determine the expressions of myelin protein zero (MPZ) andperipheral myelin protein 22 (PMP22), and expression ratio of the Bax/Bcl-2 proteins. The percentage of cell apoptosiswas evaluated by annexin V staining using flow cytometry.Results: Schwann cells under oxidative stress conditions caused by H2O2 and treated with idebenone had increasedcell viability; increased SOD, CAT, and GPx activity; and increased expressions of the MPZ and PMP22 proteins. Therewas a decreased level of MDA, a decreased expression ratio of Bax/Bcl-2 proteins, and a decrease in the percentage ofapoptotic cells stained with Annexin V.Conclusion: The appropriate dose of idebenone may improve both the survival and function of Schwann cells exposed toH2O2 by reducing oxidative stress and apoptosis.
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spelling doaj.art-bc6a39be0ee544eea1a7c21063b7a5ca2024-04-16T07:17:42ZengRoyan Institute (ACECR), TehranCell Journal2228-58062228-58142024-03-0126319420110.22074/cellj.2024.2015571.1446710540Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress ParametersSam Zarbakhsh0Parisa Hayat1Nervous System Stem Cells Research Center, Semnan University of Medical Sciences, Semnan, IranCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, IranObjective: Schwann cells are the main cells for myelination and regeneration of peripheral nerves. Idebenone is asynthetic antioxidant used to treat central nervous system diseases. The aim of the study is to determine whether idebenonecan protect Schwann cells and increase cell activity under conditions of oxidative stress caused by hydrogen peroxide(H2O2) in vitro.Materials and Methods: In this experimental study, Schwann cells were pre-treated with various concentrations ofidebenone and H2O2; after determining the appropriate doses, the cells were treated with 10 μM idebenone for 48hours and 1000 μM H2O2 for the last two hours. The malondialdehyde (MDA) level, and activity of superoxide dismutase(SOD), catalase (CAT), and glutathione peroxidase (GPx) were assessed by ELISA. Cell viability was assessed bythe MTT assay. Western blot analysis was conducted to determine the expressions of myelin protein zero (MPZ) andperipheral myelin protein 22 (PMP22), and expression ratio of the Bax/Bcl-2 proteins. The percentage of cell apoptosiswas evaluated by annexin V staining using flow cytometry.Results: Schwann cells under oxidative stress conditions caused by H2O2 and treated with idebenone had increasedcell viability; increased SOD, CAT, and GPx activity; and increased expressions of the MPZ and PMP22 proteins. Therewas a decreased level of MDA, a decreased expression ratio of Bax/Bcl-2 proteins, and a decrease in the percentage ofapoptotic cells stained with Annexin V.Conclusion: The appropriate dose of idebenone may improve both the survival and function of Schwann cells exposed toH2O2 by reducing oxidative stress and apoptosis.https://www.celljournal.org/article_710540_43b5d1b0e44c864dfae1d5d4f09fe32a.pdfapoptosisidebenoneoxidative stressschwann sells
spellingShingle Sam Zarbakhsh
Parisa Hayat
Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters
Cell Journal
apoptosis
idebenone
oxidative stress
schwann sells
title Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters
title_full Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters
title_fullStr Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters
title_full_unstemmed Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters
title_short Effects of Idebenone on Rat Schwann Cells with Toxicity Induced by Hydrogen Peroxide: Assessment of Molecular, Apoptosis, and Oxidative Stress Parameters
title_sort effects of idebenone on rat schwann cells with toxicity induced by hydrogen peroxide assessment of molecular apoptosis and oxidative stress parameters
topic apoptosis
idebenone
oxidative stress
schwann sells
url https://www.celljournal.org/article_710540_43b5d1b0e44c864dfae1d5d4f09fe32a.pdf
work_keys_str_mv AT samzarbakhsh effectsofidebenoneonratschwanncellswithtoxicityinducedbyhydrogenperoxideassessmentofmolecularapoptosisandoxidativestressparameters
AT parisahayat effectsofidebenoneonratschwanncellswithtoxicityinducedbyhydrogenperoxideassessmentofmolecularapoptosisandoxidativestressparameters