Neuregulin1 Attenuates H2O2-Induced Reductions in EAAC1 Protein Levels and Reduces H2O2-Induced Oxidative Stress
Autor: | Ji-Young Yoo, Dae-Yong Song, Sun Seek Min, Jun Ho Lee, Han-Byeol Kim, Hong-Il Yoo, Ran-Sook Woo, Tai-Kyoung Baik |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
chemistry.chemical_classification Reactive oxygen species Programmed cell death Antioxidant biology General Neuroscience medicine.medical_treatment Glutathione peroxidase Toxicology medicine.disease_cause Neuroprotection Cell biology Superoxide dismutase 03 medical and health sciences chemistry.chemical_compound 030104 developmental biology 0302 clinical medicine chemistry Lactate dehydrogenase mental disorders biology.protein medicine 030217 neurology & neurosurgery Oxidative stress |
Zdroj: | Neurotoxicity Research. 35:401-409 |
ISSN: | 1476-3524 1029-8428 |
DOI: | 10.1007/s12640-018-9965-4 |
Popis: | 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. |
Databáze: | OpenAIRE |
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