首页> 外文期刊>Brain research >Diallyl trisufide protects against oxygen glucose deprivation -induced apoptosis by scavenging free radicals via the PI3K/Akt -mediated Nrf2/HO-1 signaling pathway in B35 neural cells
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Diallyl trisufide protects against oxygen glucose deprivation -induced apoptosis by scavenging free radicals via the PI3K/Akt -mediated Nrf2/HO-1 signaling pathway in B35 neural cells

机译:通过在B35神经细胞中通过PI3K / AKT介导的NRF2 / HO-1信号通路清除自由基,将二烯丙基三硫化物防止氧血糖剥夺 - 诱导的细胞凋亡

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摘要

Oxidative stress contributes to development of ischemic brain damage. Many antioxidants have been proven effective in ameliorating cerebral ischemia injury by inhibiting oxidative stress. DATS, an organosulfuric component of garlic oil, exhibits antioxidative effects. In present study, we used OGD model to investigate the neuroprotective effects of OATS and the mechanisms related to these effects. B35 neural cells exposed to OGD caused a decrease in cell viability and increases in the percentage of apoptotic cells and the level of intracellular cleaved caspase-3, all of which were markedly attenuated by DATS. Further, OATS treatment significantly increased Nrf2 expression and nuclear translocation, upregulated downstream gene HO-1 and inhibited intracellular ROS and MDA generation, all of which were markedly attenuated in cells transfected with Nrf2-specific siRNA. In addition, inhibition of PI3K/Akt signaling by PI3K-specific siRNA not only decreased the expression level of Nrf2 and HO-1 proteins, but also diminished the antdoxidative and neuroprotective effect of DATS. Taken together, these results indicate that DATS protects B35 neural cells against OGD-induced cell injury by inhibiting ROS production via upregulating the PI3K/ Akt-mediated Nrf2 pathway, which further activates HO-1. Based on our results, OATS may be a potential candidate for intervention in hypoxic ischemic brain injuries such as stroke. (C) 2015 Elsevier B.V. All rights reserved.
机译:氧化应激有助于发展缺血性脑损伤。通过抑制氧化应激,已经证明许多抗氧化剂有效地改善脑缺血损伤。 DATS是大蒜油的有机硫磺成分,表现出抗氧化作用。在目前的研究中,我们使用OGD模型来研究燕麦的神经保护作用和与这些效果相关的机制。暴露于OGD的B35神经细胞导致细胞活力降低,并增加凋亡细胞的百分比和细胞内切割的caspase-3的水平,所有这些都通过DATS显着减弱。此外,燕麦治疗显着增加了NRF2表达和核转位,上游下游基因HO-1并抑制细胞内ROS和MDA产生,所有这些都在用NRF2特异性siRNA转染的细胞中显着减弱。此外,PI3K特异性siRNA的PI3K / AKT信号传导的抑制不仅降低了NRF2和HO-1蛋白的表达水平,还降低了DATS的抗氧化和神经保护作用。总之,这些结果表明,通过上调PI3K / AKT介导的NRF2途径来抑制ROS生产,可以通过上调PI3K / AKT介导的NRF2途径来保护B35神经细胞免受OGD诱导的细胞损伤。根据我们的结果,燕麦可能是潜在的候选人,用于干预缺氧缺血性脑损伤,如中风。 (c)2015 Elsevier B.v.保留所有权利。

著录项

  • 来源
    《Brain research》 |2015年第null期|共13页
  • 作者单位

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

    Chengdu Mil Gen Hosp Dept Geriatr Chengdu 610083 Sichuan Provice Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经病学;
  • 关键词

    Diallyl trisulfide; Oxygen glucose deprivation; Apoptosis; Reactive oxygen species; PI3K/Akt; Nrf2/HO-1;

    机译:二烯丙基三硫化物;氧葡萄糖剥夺;细胞凋亡;活性氧;PI3K / AKT;NRF2 / HO-1;

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