Transcriptional Factor NF-κB as a Target for Therapy in Parkinson's Disease

被引:90
作者
Flood, Patrick M. [1 ]
Qian, Li [1 ]
Peterson, Lynda J. [1 ]
Zhang, Feng [2 ,3 ,4 ]
Shi, Jing-Shan [2 ,3 ]
Gao, Hui-Ming [4 ]
Hong, Jau-Shyong [4 ]
机构
[1] Univ N Carolina, Dept Periodontol & Comprehens Ctr Inflammatory Di, Chapel Hill, NC 27599 USA
[2] Zunji Med Coll, Dept Pharmacol, Zunji, Peoples R China
[3] Zunji Med Coll, Key Lab Pharmacol Guizhou, Zunji, Peoples R China
[4] NIEHS, Neuropharmacol Sect, Lab Toxicol & Pharmacol, NIH, Res Triangle Pk, NC 27709 USA
关键词
SMALL-MOLECULE INHIBITOR; BINDING DOMAIN PEPTIDE; SELECTIVE-INHIBITION; KINASE-ALPHA; CELL-DEATH; IKK-BETA; NEURODEGENERATIVE DISEASES; BLOCKS OSTEOCLASTOGENESIS; CHEMOKINE EXPRESSION; DOPAMINERGIC-NEURONS;
D O I
10.4061/2011/216298
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Parkinson's disease (PD) is a neurodegenerative condition characterized by chronic inflammation. Nuclear factor kappa B (NF-kappa B) is a family of inducible transcription factors that are expressed in a wide variety of cells and tissues, including microglia, astrocytes, and neurons, and the classical NF-kappa B pathway plays a key role in the activation and regulation of inflammatory mediator production during inflammation. Activation of the classical NF-kappa B pathway is mediated through the activity of the IKK kinase complex, which consists of a heterotrimer of IKK alpha, IKK beta, and IKK gamma subunits. Targeting NF-kappa B has been proposed as an approach to the treatment of acute and chronic inflammatory conditions, and the use of inhibitors specific for either IKK beta or IKK gamma has now been found to inhibit neurodegeneration of TH+ DA-producing neurons in murine and primate models of Parkinson's disease. These studies suggest that targeting the classical pathway of NF-kappa B through the inhibition of the IKK complex can serve as a useful therapeutic approach to the treatment of PD.
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页数:8
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