Neuregulin1 Attenuates H2O2-Induced Reductions in EAAC1 Protein Levels and Reduces H2O2-Induced Oxidative Stress

被引:0
|
作者
Jun-Ho Lee
Ji-Young Yoo
Han-byeol Kim
Hong-Il Yoo
Dae-Yong Song
Sun Seek Min
Tai-Kyoung Baik
Ran-Sook Woo
机构
[1] Daejeon University,Department of Emergency Medical Technology
[2] Eulji University,Department of Anatomy and Neuroscience, College of Medicine
[3] Eulji University,Department of Physiology and Biophysics, College of Medicine
来源
Neurotoxicity Research | 2019年 / 35卷
关键词
H; O; Neuregulin 1; EAAC1; Reactive oxygen species; Superoxide dismutase; Glutathione peroxidase;
D O I
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中图分类号
学科分类号
摘要
Neuregulin 1 (NRG1) exhibits potent neuroprotective properties. The aim of the present study was to investigate the antioxidative effects and underlying mechanisms of NRG1 against H2O2-induced oxidative stress in primary rat cortical neurons. The expression level of the excitatory amino acid carrier 1 (EAAC1) protein was measured by Western blotting and immunocytochemistry. The levels of lactate dehydrogenase (LDH) release, reactive oxygen species (ROS) generation, superoxide dismutase (SOD) activity, GPx activity, and mitochondrial membrane potential (∆ψm) were determined to examine cell death and the antioxidant properties of NRG1 in primary rat cortical neurons. H2O2 reduced the expression of EAAC1 in a dose-dependent manner. We found that pretreatment with NRG1 attenuated the H2O2-induced reduction in EAAC1 expression. Moreover, NRG1 reduced the cell death and oxidative stress induced by H2O2. In addition, NRG1 attenuated H2O2-induced reductions in antioxidant enzyme activity and ∆ψm. Our data indicate a role for NRG1 in protecting against oxidative stress via the regulation of EAAC1. These observations may provide novel insights into the mechanisms of NRG1 activity during oxidative stress and may reveal new therapeutic targets for regulating the oxidative stress associated with various neurological diseases.
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页码:401 / 409
页数:8
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