Abstract
Coronary heart disease (CHD) is a hypoxia related disease. However, the relationship of the hypoxia-induced oxidative stress, autophagy and apoptosis in cardiomyocyte remains unclear. In this study, we used CoCl2 to mimic hypoxic conditions in H9c2 cardiomyocytes and study the effects of CoCl2-induced hypoxia on oxidative stress, apoptosis and autophagy, as well as the relationships among these processes. Cell viability and levels of ROS, LC3-II, p62, caspase-3 and PARP were assessed. The viability and morphology of cardiomyocytes were affected by hypoxia, and hypoxia enhanced levels of ROS and the levels of the LC3-II, p62, caspase-3 and PARP proteins in H9c2 cells in a dose-dependent manner. ROS levels rise gradually in the presence of hypoxia; however, it shrinks when hypoxia reaches a certain level. Caspase-3 and PARP levels were raised with the increasing of hypoxia level. Enhanced level of LC3 and decreased levels of p62 in hypoxic cells indicate that autophagy levels are in accord with hypoxia. Based on these results, hypoxia induces oxidative stress, apoptosis and autophagy in cardiomyocytes. Autophagy is a double-edged sword. At a low level, autophagy can resist oxidative stress and protect cardiomyocytes from oxidative stress, while high level autophagy can promote apoptosis of cardiomyocytes.
Highlights
The viability and morphology of cardiomyocytes were affected by hypoxia, and hypoxia enhanced levels of reactive oxygen species (ROS) and the levels of the LC3-II, p62, caspase-3 and Poly ADP-ribose polymerase (PARP) proteins in H9c2 cells in a dose-dependent manner
Little information is known about the relationships among these processes in cardiomyocytes which limited our understanding of the roles of oxidative stress, autophagy and apoptosis in the progression of human diseases [5]
We examined the relationships among oxidative stress, apoptosis and autophagy
Summary
Coronary heart disease (CHD) is the leading cause of death in older men and women in the western world, and reduced oxygen availability may cause or ex-. Acerbate symptoms of CHD [1]. A constant oxygen supply is essential for cardiac viability and function. Hypoxia induces some pathological process, such as oxidative stress, autophagy and apoptosis [2] [3] [4]. Researchers have obtained a good understanding of individual pathological processes induced by hypoxia. Little information is known about the relationships among these processes in cardiomyocytes which limited our understanding of the roles of oxidative stress, autophagy and apoptosis in the progression of human diseases [5]
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