首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Cerebral Dopamine Neurotrophic Factor (CDNF) Has Neuroprotective Effects against Cerebral Ischemia That May Occur through the Endoplasmic Reticulum Stress Pathway
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Cerebral Dopamine Neurotrophic Factor (CDNF) Has Neuroprotective Effects against Cerebral Ischemia That May Occur through the Endoplasmic Reticulum Stress Pathway

机译:脑多巴胺神经营养因子(CDNF)对可能通过内质网应激途径发生的脑缺血具有神经保护作用

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摘要

Cerebral dopamine neurotrophic factor (CDNF), previously known as the conserved dopamine neurotrophic factor, belongs to the evolutionarily conserved CDNF/mesencephalic astrocyte-derived neurotrophic factor MANF family of neurotrophic factors that demonstrate neurotrophic activities in dopaminergic neurons. The function of CDNF during brain ischemia is still not known. MANF is identified as an endoplasmic reticulum (ER) stress protein; however, the role of CDNF in ER stress remains to be fully elucidated. Here, we test the neuroprotective effect of CDNF on middle cerebral artery occlusion (MCAO) rats and neurons and astrocytes treated with oxygen–glucose depletion (OGD). We also investigate the expression of CDNF in cerebral ischemia and in primary neurons treated with ER stress-inducing agents. Our results show that CDNF can significantly reduce infarct volume, reduce apoptotic cells and improve motor function in MCAO rats, while CDNF can increase the cell viability of neurons and astrocytes treated by OGD. The expression of CDNF was upregulated in the peri-infarct tissue at 2 h of ischemia/24 h reperfusion. ER stress inducer can induce CDNF expression in primary cultured neurons. Our data indicate that CDNF has neuroprotective effects on cerebral ischemia and the OGD cell model and the protective mechanism of CDNF may occur through ER stress pathways.
机译:脑多巴胺神经营养因子(CDNF),以前称为保守的多巴胺神经营养因子,属于进化保守的CDNF /中脑星形胶质细胞衍生的神经营养因子MANF家族的神经营养因子,可证明多巴胺能神经元具有神经营养活性。 CDNF在脑缺血期间的功能仍然未知。 MANF被鉴定为内质网(ER)应激蛋白;然而,CDNF在内质网应激中的作用仍有待充分阐明。在这里,我们测试了CDNF对大脑中动脉闭塞(MCAO)大鼠以及经氧葡萄糖耗竭(OGD)处理的神经元和星形胶质细胞的神经保护作用。我们还研究了CDNF在脑缺血和用ER应激诱导剂治疗的原代神经元中的表达。我们的结果表明,CDNF可以显着减少MCAO大鼠的梗塞体积,减少凋亡细胞并改善运动功能,而CDNF可以增加OGD处理的神经元和星形胶质细胞的细胞活力。在缺血2小时/ 24 h再灌注后,梗死周围组织中CDNF的表达上调。 ER应激诱导剂可诱导原代培养神经元中CDNF的表达。我们的数据表明CDNF对脑缺血和OGD细胞模型具有神经保护作用,而CDNF的保护机制可能是通过ER应激途径发生的。

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