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Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species

Objective. Artemisia ciniformis (Asteraceae) and A. biennis are two of 34 Artemisia species growing naturally in Iran. In this study we investigated whether different extracts of A. ciniformis and A. biennis have protective effect against hydrogen peroxide-induced cytotoxicity in rat cardiomyoblast...

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Autores principales: Mojarrab, Mahdi, Jamshidi, Maryam, Ahmadi, Farahnaz, Alizadeh, Ellahe, Hosseinzadeh, Leila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867950/
https://www.ncbi.nlm.nih.gov/pubmed/24381586
http://dx.doi.org/10.1155/2013/141683
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author Mojarrab, Mahdi
Jamshidi, Maryam
Ahmadi, Farahnaz
Alizadeh, Ellahe
Hosseinzadeh, Leila
author_facet Mojarrab, Mahdi
Jamshidi, Maryam
Ahmadi, Farahnaz
Alizadeh, Ellahe
Hosseinzadeh, Leila
author_sort Mojarrab, Mahdi
collection PubMed
description Objective. Artemisia ciniformis (Asteraceae) and A. biennis are two of 34 Artemisia species growing naturally in Iran. In this study we investigated whether different extracts of A. ciniformis and A. biennis have protective effect against hydrogen peroxide-induced cytotoxicity in rat cardiomyoblast cells (H9c2). Method. The dried and ground aerial parts of these two species were extracted successively using petroleum ether (40–60), dichloromethane, ethyl acetate (EA), ethanol (EtOH) and ethanol : water (1 : 1) by maceration method. To evaluate whether different extracts of A. ciniformis and A. biennis protect cardiomyoblast H9c2 cells from H(2)O(2) cytotoxicity, we examined the direct cytotoxic effect of H(2)O(2) on H9c2 cells in the presence and absence of different extracts. After then, cell viability was measured by MTT assay. Results. H(2)O(2) induced cytotoxicity in a concentration dependent manner. The IC(50) value was 62.5 μM for 24 h exposure. However, pretreatment of cells with various concentrations of EA, EtOH, and EtOH/wt extract of A. ciniformis protected cells from H(2)O(2)-induced cytotoxicity. Moreover, pretreatment with EA, EtOH and EtOH/wt extracts of A. ciniformis lead to a decrease in the reactive oxygen species (ROS) generation. Taken together our observation indicated that nontoxic concentration of different extracts of A. ciniformis has protective effect on H(2)O(2)-induced cytotoxicity in H9c2 cells.
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spelling pubmed-38679502013-12-31 Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species Mojarrab, Mahdi Jamshidi, Maryam Ahmadi, Farahnaz Alizadeh, Ellahe Hosseinzadeh, Leila Adv Pharmacol Sci Research Article Objective. Artemisia ciniformis (Asteraceae) and A. biennis are two of 34 Artemisia species growing naturally in Iran. In this study we investigated whether different extracts of A. ciniformis and A. biennis have protective effect against hydrogen peroxide-induced cytotoxicity in rat cardiomyoblast cells (H9c2). Method. The dried and ground aerial parts of these two species were extracted successively using petroleum ether (40–60), dichloromethane, ethyl acetate (EA), ethanol (EtOH) and ethanol : water (1 : 1) by maceration method. To evaluate whether different extracts of A. ciniformis and A. biennis protect cardiomyoblast H9c2 cells from H(2)O(2) cytotoxicity, we examined the direct cytotoxic effect of H(2)O(2) on H9c2 cells in the presence and absence of different extracts. After then, cell viability was measured by MTT assay. Results. H(2)O(2) induced cytotoxicity in a concentration dependent manner. The IC(50) value was 62.5 μM for 24 h exposure. However, pretreatment of cells with various concentrations of EA, EtOH, and EtOH/wt extract of A. ciniformis protected cells from H(2)O(2)-induced cytotoxicity. Moreover, pretreatment with EA, EtOH and EtOH/wt extracts of A. ciniformis lead to a decrease in the reactive oxygen species (ROS) generation. Taken together our observation indicated that nontoxic concentration of different extracts of A. ciniformis has protective effect on H(2)O(2)-induced cytotoxicity in H9c2 cells. Hindawi Publishing Corporation 2013 2013-12-04 /pmc/articles/PMC3867950/ /pubmed/24381586 http://dx.doi.org/10.1155/2013/141683 Text en Copyright © 2013 Mahdi Mojarrab et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mojarrab, Mahdi
Jamshidi, Maryam
Ahmadi, Farahnaz
Alizadeh, Ellahe
Hosseinzadeh, Leila
Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species
title Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species
title_full Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species
title_fullStr Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species
title_full_unstemmed Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species
title_short Extracts of Artemisia ciniformis Protect Cytotoxicity Induced by Hydrogen Peroxide in H9c2 Cardiac Muscle Cells through the Inhibition of Reactive Oxygen Species
title_sort extracts of artemisia ciniformis protect cytotoxicity induced by hydrogen peroxide in h9c2 cardiac muscle cells through the inhibition of reactive oxygen species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3867950/
https://www.ncbi.nlm.nih.gov/pubmed/24381586
http://dx.doi.org/10.1155/2013/141683
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