首页> 美国卫生研究院文献>Aging (Albany NY) >A phenolic amide (LyA) isolated from the fruits of Lycium barbarum protects against cerebral ischemia–reperfusion injury via PKCε/Nrf2/HO-1 pathway
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A phenolic amide (LyA) isolated from the fruits of Lycium barbarum protects against cerebral ischemia–reperfusion injury via PKCε/Nrf2/HO-1 pathway

机译:从枸杞子中分离得到的酚酰胺(LyA)通过PKCε/ Nrf2 / HO-1途径预防脑缺血-再灌注损伤

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摘要

Lyciumamide A (LyA), a dimer of phenolic amide isolated from the fruits of has been confirmed to possess potent antioxidant activity. This study was aimed to investigate the neuroprotection and molecular mechanisms of LyA against cerebral ischemia/reperfusion (I/R) injury via improving antioxidant activity. The model of middle cerebral artery occlusion (MCAO) and SH-SY5Y cells induced by oxygen and glucose deprivation (OGD) were adopted to verify the neuroprotective effects and the potential pharmacology mechanisms of LyA and . In MCAO model, treatment with LyA significantly improved neurologic score, reduced infarct volume, and relieved oxidative stress injury at 48 h after reperfusion. Meanwhile, LyA markedly increased the transcription Nrf2 and HO-1 expressions in the ischemic cerebral cortex. In vitro results showed that LyA protected differentiated SH-SY5Y cells against OGD-induced injury. LyA significantly decreased the expression of caspase-3 and the Bax/Bcl-2 ratio. But knockdown of Nrf2 or HO-1 attenuated the protective effect of LyA. Similarly, knockdown of protein kinase Cε (PKCε) inhibited LyA-induced Nrf2/HO-1 activation, and abated its protective effects. In conclusion, this study firstly demonstrated that LyA protects against cerebral I/R injury, ameliorates oxidative damage and neuronal apoptosis, partly via activation of PKCε/Nrf2/HO-1 pathway.
机译:业已确认从水果中分离出的酚酰胺的二聚体Lyciumamide A(LyA)具有有效的抗氧化活性。这项研究旨在探讨LyA通过改善抗氧化活性来对抗脑缺血/再灌注(I / R)损伤的神经保护作用和分子机制。采用氧和葡萄糖剥夺(OGD)诱导的大脑中动脉闭塞(MCAO)和SH-SY5Y细胞模型来验证LyA和LyA的神经保护作用和潜在的药理机制。在MCAO模型中,在再灌注后48 h,LyA治疗可显着改善神经系统评分,减少梗塞体积并减轻氧化应激损伤。同时,LyA明显增加缺血性大脑皮层的转录Nrf2和HO-1表达。体外结果显示,LyA保护分化的SH-SY5Y细胞免受OGD诱导的损伤。 LyA显着降低caspase-3的表达和Bax / Bcl-2的比率。但是敲低Nrf2或HO-1减弱了LyA的保护作用。同样,敲除蛋白激酶Cε(PKCε)抑制LyA诱导的Nrf2 / HO-1活化,并减弱其保护作用。总之,这项研究首先证明了LyA可以部分地通过激活PKCε/ Nrf2 / HO-1途径来预防脑I / R损伤,改善氧化损伤和神经细胞凋亡。

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