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Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro

BACKGROUND: Sugemule-3 (SD) is a traditional Chinese medicine with protective effect of myocardium. However, the underlying mechanisms of the effect had not been elucidated. MATERIALS AND METHODS: In the present study, the serum of SD was prepared. A model of β-adrenergic agonist isoprenaline (ISO)-...

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Autores principales: Wang, Yu, Gong, Guo-Hua, Xu, Ya-Nan, Yu, Li-Jun, Wei, Cheng-Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551375/
https://www.ncbi.nlm.nih.gov/pubmed/28839382
http://dx.doi.org/10.4103/0973-1296.211018
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author Wang, Yu
Gong, Guo-Hua
Xu, Ya-Nan
Yu, Li-Jun
Wei, Cheng-Xi
author_facet Wang, Yu
Gong, Guo-Hua
Xu, Ya-Nan
Yu, Li-Jun
Wei, Cheng-Xi
author_sort Wang, Yu
collection PubMed
description BACKGROUND: Sugemule-3 (SD) is a traditional Chinese medicine with protective effect of myocardium. However, the underlying mechanisms of the effect had not been elucidated. MATERIALS AND METHODS: In the present study, the serum of SD was prepared. A model of β-adrenergic agonist isoprenaline (ISO)-induced H9c2 cardiomyocytes injury was established in vitro. The changes in cell viability were examined to determine the available concentration of ISO and serum of SD. ELISA, terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling assay, and flow cytometry were used to detect the effect of serum of SD on oxidative stress and apoptosis. The expression levels of the mitochondria-dependent apoptotic pathway and mitogen-activated protein kinase signalling-related proteins were analyzed. RESULTS: Incubation with different dose of ISO (0.015, 0.01, 0.005, and 0.0025 mol/L) for 24 h caused dose-dependent loss of cell viability and 0.01 mol/L of ISO approximately reduced the cell viability to 50%. Pretreatment with 50 μ mol/L serum of SD effectively decreased the levels of ISO-induced cell toxicity. Serum of SD relived ISO-induced oxidative stress and apoptosis in H9c2 cardiomyocytes. A further mechanism study indicated that serum of SD inhibited the mitochondria-dependent apoptotic pathways and regulated the expression levels of Bcl-2 family. ISO activated ERK and P38, whereas serum of SD inhibited their activation. CONCLUSION: Serum of SD inhibits the ISO-induced activation of the mitochondria-dependent apoptotic pathway, oxidative stress, and ERK, P38 inactivation. Serum of SD is used for the treatment of ISO-induced cardiomyopathy. SUMMARY: The serum of SD pretreatment significantly ameliorated ISO-induced H9c2 cardiomyocytes injuries. The protective effect related with apoptosis and oxidative stress. Inhibition of MAPK pathway was involed in serum of SD induced cardioprotection. The serum of SD is used for the treatment of ISO-induced cardiomyopathy. Abbreviations used: ELISA: Enzyme-linked Immunosorbent Assay; TUNEL: TdT-mediated dUTP nick end labeling; MTT: 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide, DMSO: dimethyl sulfoxide; MDA: Malondialdehyde; SOD: Superoxide Dismutase; GSH-Px: Glutathione peroxidase.
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spelling pubmed-55513752017-08-24 Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro Wang, Yu Gong, Guo-Hua Xu, Ya-Nan Yu, Li-Jun Wei, Cheng-Xi Pharmacogn Mag Original Article BACKGROUND: Sugemule-3 (SD) is a traditional Chinese medicine with protective effect of myocardium. However, the underlying mechanisms of the effect had not been elucidated. MATERIALS AND METHODS: In the present study, the serum of SD was prepared. A model of β-adrenergic agonist isoprenaline (ISO)-induced H9c2 cardiomyocytes injury was established in vitro. The changes in cell viability were examined to determine the available concentration of ISO and serum of SD. ELISA, terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling assay, and flow cytometry were used to detect the effect of serum of SD on oxidative stress and apoptosis. The expression levels of the mitochondria-dependent apoptotic pathway and mitogen-activated protein kinase signalling-related proteins were analyzed. RESULTS: Incubation with different dose of ISO (0.015, 0.01, 0.005, and 0.0025 mol/L) for 24 h caused dose-dependent loss of cell viability and 0.01 mol/L of ISO approximately reduced the cell viability to 50%. Pretreatment with 50 μ mol/L serum of SD effectively decreased the levels of ISO-induced cell toxicity. Serum of SD relived ISO-induced oxidative stress and apoptosis in H9c2 cardiomyocytes. A further mechanism study indicated that serum of SD inhibited the mitochondria-dependent apoptotic pathways and regulated the expression levels of Bcl-2 family. ISO activated ERK and P38, whereas serum of SD inhibited their activation. CONCLUSION: Serum of SD inhibits the ISO-induced activation of the mitochondria-dependent apoptotic pathway, oxidative stress, and ERK, P38 inactivation. Serum of SD is used for the treatment of ISO-induced cardiomyopathy. SUMMARY: The serum of SD pretreatment significantly ameliorated ISO-induced H9c2 cardiomyocytes injuries. The protective effect related with apoptosis and oxidative stress. Inhibition of MAPK pathway was involed in serum of SD induced cardioprotection. The serum of SD is used for the treatment of ISO-induced cardiomyopathy. Abbreviations used: ELISA: Enzyme-linked Immunosorbent Assay; TUNEL: TdT-mediated dUTP nick end labeling; MTT: 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide, DMSO: dimethyl sulfoxide; MDA: Malondialdehyde; SOD: Superoxide Dismutase; GSH-Px: Glutathione peroxidase. Medknow Publications & Media Pvt Ltd 2017 2017-07-19 /pmc/articles/PMC5551375/ /pubmed/28839382 http://dx.doi.org/10.4103/0973-1296.211018 Text en Copyright: © 2017 Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Wang, Yu
Gong, Guo-Hua
Xu, Ya-Nan
Yu, Li-Jun
Wei, Cheng-Xi
Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro
title Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro
title_full Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro
title_fullStr Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro
title_full_unstemmed Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro
title_short Sugemule-3 Protects against Isoprenaline-induced Cardiotoxicity In vitro
title_sort sugemule-3 protects against isoprenaline-induced cardiotoxicity in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551375/
https://www.ncbi.nlm.nih.gov/pubmed/28839382
http://dx.doi.org/10.4103/0973-1296.211018
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