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

机译:Neuregulin1减轻H2O2诱导的EAAC1蛋白水平的降低并降低H2O2诱导的氧化应激

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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.
机译:神经调节蛋白1(NRG1)具有强大的神经保护作用。本研究的目的是研究NRG1对H2O2诱导的原代大鼠皮层神经元氧化应激的抗氧化作用及其潜在机制。通过蛋白质印迹和免疫细胞化学测量兴奋性氨基酸载体1(EAAC1)蛋白的表达水平。测定乳酸脱氢酶(LDH)释放水平,活性氧(ROS)产生,超氧化物歧化酶(SOD)活性,GPx活性和线粒体膜电位(∆ψm),以检查原代细胞死亡和NRG1的抗氧化特性大鼠皮质神经元。 H2O2以剂量依赖性方式降低EAAC1的表达。我们发现用NRG1预处理减弱了H2O2诱导的EAAC1表达的降低。此外,NRG1减少了H2O2诱导的细胞死亡和氧化应激。此外,NRG1减弱了H2O2引起的抗氧化酶活性和∆ψm的降低。我们的数据表明NRG1在通过调节EAAC1抵抗氧化应激中的作用。这些观察结果可能会提供有关氧化应激期间NRG1活性机制的新颖见解,并可能揭示调节与各种神经系统疾病相关的氧化应激的新治疗靶标。

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