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首页> 外文期刊>Brain research bulletin >Electroacupuncture pretreatment prevents ischemic stroke and inhibits Wnt signaling-mediated autophagy through the regulation of GSK-3 beta phosphorylation
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Electroacupuncture pretreatment prevents ischemic stroke and inhibits Wnt signaling-mediated autophagy through the regulation of GSK-3 beta phosphorylation

机译:电针预处理可防止缺血性卒中,并通过调节GSK-3β磷酸化来抑制WNT信号传导的自噬

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摘要

Electroacupuncture (EA), a traditional Chinese replacement therapy, is widely accepted to treat ischemic stroke. Increasing evidence show that autophagy is involved in the process of cerebral ischemia injury and the Wnt/GSK3 beta pathway, playing an important role in protecting central nervous system. In this study, rats were treated with EA prior to focal ischemia by middle cerebral artery occlusion (MCAO). Deficit score, infarct volumes and levels of autophagy markers, such as LC3I, LC3II and p62, were assessed with either PI3K inhibitor wortmannin or a GSK-3 beta inhibitor LiCl. Oxygen-glucose deprivation/re-oxygenation (OGD/R) was made in the primitive neuron in vitro, and was respectively treated with autophagy inhibitors 3-MA, LiCl, GSK3 beta siRNA, or mTOR inhibitor rapamycin. The results indicated that EA pretreatment increased the levels of autophagy marker LC3-II and reduced the levels of p62. Meanwhile, deficit outcome was improved, and infarct volumes were reduced by EA pretreatment. Furthermore, the beneficial effects of EA pretreatment were reversed by wortmannin. LiCl and GSK3 beta siRNA can mimic the neuroprotective effects of EA pretreatment by downregulating autophagy, and increasing protein levels of p-mTOR, p-GSK3 beta and beta-catenin in OGD/R neurons. However, the protective effects of GSK3 beta siRNA were blocked by rapamycin. These results suggest that EA pretreatment induces tolerance to cerebral ischemia by inhibiting autophagy via the Wnt pathway through the inhibition of GSK3 beta.
机译:一种传统的中药替代治疗,广泛接受电针(EA),以治疗缺血性卒中。越来越多的证据表明,自噬参与了脑缺血损伤和WNT / GSK3β途径的过程,在保护中枢神经系统中发挥着重要作用。在这项研究中,通过中脑动脉闭塞(MCAO)在局灶性缺血之前用EA对大鼠进行治疗。使用PI3K抑制剂Wortmannin或GSK-3β抑制剂LiCl评估缺陷评分,梗塞体积和自噬标志物,例如LC3I,LC3II和P62的水平。在体外,在原始神经元中制备氧葡萄糖剥夺/重新氧合(OGD / R),并分别用自噬抑制剂3-MA,LICL,GSK3βsiRNA或MTOR抑制剂雷帕霉素处理。结果表明,EA预处理增加了自噬标志物LC3-II的水平,降低了P62的水平。同时,改善了赤字结果,EA预处理减少了梗塞体积。此外,韦尔曼本林逆转EA预处理的有益效果。 LiCl和GSK3βsiRNA可以模仿EA预处理的神经保护作用,通过下调自噬,增加P-MTOR,P-GSK3β和β-连环蛋白在OGD / R神经元中的蛋白质水平。然而,通过雷帕霉素阻断GSK3βsiRNA的保护作用。这些结果表明EA预处理通过抑制GSK3β通过WNT途径抑制自噬诱导对脑缺血的耐受性。

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