Molecular identification for epigallocatechin-3-gallate-mediated antioxidant intervention on the H2O2-induced oxidative stress in H9c2 rat cardiomyoblastsReportar como inadecuado

Molecular identification for epigallocatechin-3-gallate-mediated antioxidant intervention on the H2O2-induced oxidative stress in H9c2 rat cardiomyoblasts - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Journal of Biomedical Science

, 21:56

First Online: 09 June 2014Received: 19 February 2014Accepted: 03 June 2014DOI: 10.1186-1423-0127-21-56

Cite this article as: Chen, WC., Hsieh, SR., Chiu, CH. et al. J Biomed Sci 2014 21: 56. doi:10.1186-1423-0127-21-56


BackgroundEpigallocatechin-3-gallate EGCG has been documented for its beneficial effects protecting oxidative stress to cardiac cells. Previously, we have shown the EGCG-mediated cardiac protection by attenuating reactive oxygen species and cytosolic Ca in cardiac cells during oxidative stress and myocardial ischemia. Here, we aimed to seek a deeper elucidation of the molecular anti-oxidative capabilities of EGCG in an H2O2-induced oxidative stress model of myocardial ischemia injury using H9c2 rat cardiomyoblasts.

ResultsProteomics analysis was used to determine the differential expression of proteins in H9c2 cells cultured in the conditions of control, 400 μM H2O2 exposure for 30 min with and-or without 10 to 20 μM EGCG pre-treatment. In this model, eight proteins associated with energy metabolism, mitochondrial electron transfer, redox regulation, signal transduction, and RNA binding were identified to take part in EGCG-ameliorating H2O2-induced injury in H9c2 cells. H2O2 exposure increased oxidative stress evidenced by increases in reactive oxygen species and cytosolic Ca overload, increases in glycolytic protein, α-enolase, decreases in antioxidant protein, peroxiredoxin-4, as well as decreases in mitochondrial proteins, including aldehyde dehydrogenase-2, ornithine aminotransferase, and succinate dehydrogenase ubiquinone flavoprotein subunit. All of these effects were reversed by EGCG pre-treatment. In addition, EGCG attenuated the H2O2-induced increases of Type II inositol 3, 4-bisphosphate 4-phosphatase and relieved its subsequent inhibition of the downstream signalling for Akt and glycogen synthase kinase-3β GSK-3β-cyclin D1 in H9c2 cells. Pre-treatment with EGCG or GSK-3β inhibitor SB 216763 significantly improved the H2O2-induced suppression on cell viability, phosphorylation of pAkt S473 and pGSK-3β S9, and level of cyclin D1 in cells.

ConclusionsCollectively, these findings suggest that EGCG blunts the H2O2-induced oxidative effect on the Akt activity through the modulation of PIP3 synthesis leading to the subsequent inactivation of GSK-3β mediated cardiac cell injury.

KeywordsEGCG H9c2 Oxidative stress Proteomics analysis Survival pathway Electronic supplementary materialThe online version of this article doi:10.1186-1423-0127-21-56 contains supplementary material, which is available to authorized users.

Wei-Cheng Chen, Shih-Rong Hsieh contributed equally to this work.

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Autor: Wei-Cheng Chen - Shih-Rong Hsieh - Chun-Hwei Chiu - Ban-Dar Hsu - Ying-Ming Liou


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