标题:Rosiglitazone protects dopaminergic neurons against lipopolysaccharide- induced neurotoxicity through inhibition of microglia activation
作者:He,X.;Feng,L.;Meng,H.;Wang,X.;Liu,S.
作者机构:Department of Anatomy, Shandong University School of Medicine, 44 Wenhua xilu, Jinan, Shandong;Department of Anatomy, Shandong U
通讯作者:Liu, SW
通讯作者地址:[Liu, SW]Shandong Univ, Dept Anat, Sch Med, 44 Wenhua Xilu, Jinan 250012, Shandong, Peoples R China.
来源:International Journal of Neuroscience
出版年:2012
卷:122
期:9
页码:532-540
DOI:10.3109/00207454.2012.686544
关键词:dopaminergic neurons;microglia;Parkinson\'s disease;rosiglitazone
摘要:Recent evidence has suggested that microglia activation plays an important role in the pathogenesis of Parkinson\'s disease (PD). Activated microglia secrete various proinflammatory cytokines and neurotoxic mediators, which may contribute to the development of PD. Thus, the inhibition of microglia activation may have a therapeutic benefit in the treatment of PD. In the present study, using mesencephalic neuronmicroglia mixed culture and microglia-enriched culture, we investigated whether rosiglitazone (RGZ), a member of peroxisome proliferator-activated receptor gamma (PPARγ) agonists, could inhibit microglia activation. Our results showed that RGZ significantly inhibited lipopolysaccharide (LPS)-induced microglia activation and the production of tumor necrosis factor-alpha (TNF-α), nitric oxide (NO), and superoxide. We further investigated the intracellular signaling pathways regulating the production of TNF-α and NO in LPS-activated microglia. The results showed that RGZ inhibited the phosphorylation and nuclear translocation of the p65 subunit of NF-κB, and the phosphorylation of p38 mitogen-activated protein kinase (p38MAPK). Taken together, our results suggested that the therapeutic effects of RGZ were partially mediated by modulating microglia activation.
收录类别:SCIE
WOS核心被引频次:6
资源类型:期刊论文
TOP