Int J Med Sci 2016; 13(8):646-652. doi:10.7150/ijms.15177

Research Paper

NOX2 Antisense Attenuates Hypoxia-Induced Oxidative Stress and Apoptosis in Cardiomyocyte

Bo Yu, Fanbo Meng, Yushuang Yang, Dongna Liu, Kaiyao Shi

Department of cardiology, China-Japan union hospital of Jilin University, Changchun, Jilin, 130033, P.R. China

Abstract

Heart ischemia is a hypoxia related disease. NOX2 and HIF-1α proteins were increased in cardiomyocytes after acute myocardial infarction. However, the relationship of the hypoxia-induced HIF-1α. NOX2-derived oxidative stress and apoptosis in cardiomyocyte remains unclear. In the current study, we use NOX2 antisense strategy to investigate the role of NOX2 in hypoxia-induced oxidative stress and apoptosis in rat cardiomyocytes. Here, we show that transduction of ADV-NOX2-AS induces potent silencing of NOX2 in cardiomyocytes, and resulting in attenuation of hypoxia-induced oxidative stress and apoptosis. This study indicates the potential of antisense-based therapies and validates NOX2 as a potent therapeutic candidate for heart ischemia.

Keywords: Heart ischemia, Heart infarction, NOX2, Oxidative stress, and apoptosis

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How to cite this article:
Yu B, Meng F, Yang Y, Liu D, Shi K. NOX2 Antisense Attenuates Hypoxia-Induced Oxidative Stress and Apoptosis in Cardiomyocyte. Int J Med Sci 2016; 13(8):646-652. doi:10.7150/ijms.15177. Available from http://www.medsci.org/v13p0646.htm