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

被引:46
作者
Kaewmool, Chayanut [1 ]
Kongtawelert, Prachya [1 ]
Phitak, Thanyaluck [1 ]
Pothacharoen, Peraphan [1 ]
Udomruk, Sasimol [1 ]
机构
[1] Chiang Mai Univ, Fac Med, Thailand Excellence Ctr Tissue Engn & Stem Cells, Dept Biochem, Chiang Mai 50200, Thailand
关键词
Protocatechuic acid; Microglial activation; SIRT1; Neuronal apoptosis; Neurodegenerative diseases; NF-KAPPA-B; GENE-EXPRESSION; NEURONAL APOPTOSIS; OXIDATIVE STRESS; DOWN-REGULATION; BRAIN-INJURY; SIRT1; LIPOPOLYSACCHARIDE; MECHANISMS; NEUROINFLAMMATION;
D O I
10.1016/j.jneuroim.2020.577164
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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-kappa B 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.
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页数:11
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