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原儿茶酸通过调控 SIRT1/NF-κB 通路抑制 LPS 激活的 BV2 小胶质细胞炎症反应进而抑制小胶质细胞激活诱导的 PC12 细胞凋亡。

Protocatechuic acid inhibits inflammatory responses in LPS-activated BV2 microglia via regulating SIRT1/NF-κB pathway contributed to the suppression of microglial activation-induced PC12 cell apoptosis.

机构信息

Thailand Excellence Center for Tissue Engineering and Stem Cells, Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

Thailand Excellence Center for Tissue Engineering and Stem Cells, Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

J Neuroimmunol. 2020 Apr 15;341:577164. doi: 10.1016/j.jneuroim.2020.577164. Epub 2020 Jan 18.

Abstract

SIRT1 exhibits inhibitory effects on microglial activation-induced neurodegeneration. Regulating SIRT1 may become a novel approach for curing neurodegenerative diseases. Protocatechuic acid (PA), a phenolic acid, has anti-neuroinflammatory effects. The effect of PA on SIRT1 in activated microglia remains unknown. Here, we examined whether PA has anti-inflammatory effects against microglial activation-induced neuronal cell death via regulating SIRT1 in microglia. We found that PA inhibited the release of inflammatory mediators in LPS-activated BV2 microglia via the SIRT1/NF-κB pathway and thereby attenuated microglial activation-induced PC12 cell apoptosis. This suggests that SIRT1 mediates the anti-neuroinflammatory effects of PA to ameliorate microglial activation-induced neuron death.

摘要

SIRT1 对小胶质细胞激活诱导的神经退行性变具有抑制作用。调节 SIRT1 可能成为治疗神经退行性疾病的新方法。原儿茶酸(PA)是一种酚酸,具有抗神经炎症作用。PA 对激活的小胶质细胞中 SIRT1 的影响尚不清楚。在这里,我们研究了 PA 是否通过调节小胶质细胞中的 SIRT1 来抑制 LPS 激活的 BV2 小胶质细胞中炎症介质的释放,从而减轻小胶质细胞激活诱导的 PC12 细胞凋亡。这表明 SIRT1 介导了 PA 的抗神经炎症作用,以改善小胶质细胞激活诱导的神经元死亡。

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