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首页> 外文期刊>Neurochemical Research >Dietary Supplementation with tBHQ, an Nrf2 Stabilizer Molecule, Confers Neuroprotection Against Apoptosis in Amyloid β-Injected Rat
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Dietary Supplementation with tBHQ, an Nrf2 Stabilizer Molecule, Confers Neuroprotection Against Apoptosis in Amyloid β-Injected Rat

机译:膳食补充tBHQ(一种Nrf2稳定剂分子)可为注射淀粉样蛋白的大鼠提供抗凋亡的神经保护作用

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摘要

Nuclear factor erythroid 2-related factor 2 (Nrf2) coordinates the up-regulation of cytoprotective genes via the antioxidant response element (ARE). There is significant evidence that oxidative stress is a critical event in the pathogenesis of AD. Considering the protective role of Nrf2 against oxidative injury, we studied to determine whether in vivo toxicity of amyloid β (Aβ) can be attenuated by tBHQ, an Nrf2 stabilizer, Using an Aβ injection model. We demonstrated that pre-activation of endogenous Nrf2 by tBHQ attenuated Aβ-induced caspase-3 expression. tBHQ enhanced GSH, decreased MDA level, and inhibited NF-κB. This investigation provides the first documentation of tBHQ’s neuroprotective effect through decrease of Aβ accumulation in rat brain. Our results show the involvement of Hsp-70 in this protective effect. In summary tBHQ treatment for 1 week prior to Aβ injection protected against the oxidative damage, apoptosis and Aβ accumulation in rats.
机译:核因子红系2相关因子2(Nrf2)通过抗氧化剂反应元件(ARE)协调细胞保护基因的上调。有大量证据表明氧化应激是AD发病机理中的关键事件。考虑到Nrf2对氧化损伤的保护作用,我们研究了使用Aβ注射模型确定Nbf2稳定剂tBHQ是否可以减弱淀粉样蛋白β(Aβ)的体内毒性。我们证明了tBHQ对内源性Nrf2的预激活减弱了Aβ诱导的caspase-3表达。 tBHQ增强GSH,降低MDA水平,并抑制NF-κB。这项研究首次证明了tBHQ通过减少大鼠脑内Aβ积累而产生的神经保护作用。我们的结果表明Hsp-70参与了这种保护作用。总之,在注射Aβ之前1周的tBHQ治疗可防止大鼠的氧化损伤,细胞凋亡和Aβ积累。

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