Shikimic Acid Promotes Oligodendrocyte Precursor Cell Differentiation and Accelerates Remyelination in Mice

被引:17
|
作者
Lu, Fengfeng [1 ,2 ,3 ]
Yin, Dou [1 ,2 ,3 ]
Pu, Yingyan [2 ,3 ]
Liu, Weili [1 ,2 ,3 ]
Li, Zhenghao [2 ,3 ]
Shao, Qi [2 ,3 ]
He, Cheng [1 ,2 ,3 ]
Cao, Li [2 ,3 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Hefei 230601, Anhui, Peoples R China
[2] Second Mil Med Univ, Minist Educ, Inst Neurosci, Key Lab Mol Neurobiol, Shanghai 200433, Peoples R China
[3] Second Mil Med Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Shikimic acid; Oligodendrocyte precursor cells; Demyelination; Remyelination; MULTIPLE-SCLEROSIS; OXIDATIVE STRESS; MAMMALIAN TARGET; PROGENITOR CELLS; CNS; ACTIVATION; MICROGLIA; MTOR; DEMYELINATION; POLARIZATION;
D O I
10.1007/s12264-018-0322-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The obstacle to successful remyelination in demyelinating diseases, such as multiple sclerosis, mainly lies in the inability of oligodendrocyte precursor cells (OPCs) to differentiate, since OPCs and oligodendrocyte-lineage cells that are unable to fully differentiate are found in the areas of demyelination. Thus, promoting the differentiation of OPCs is vital for the treatment of demyelinating diseases. Shikimic acid (SA) is mainly derived from star anise, and is reported to have anti-influenza, anti-oxidation, and anti-tumor effects. In the present study, we found that SA significantly promoted the differentiation of cultured rat OPCs without affecting their proliferation and apoptosis. In mice, SA exerted therapeutic effects on experimental autoimmune encephalomyelitis (EAE), such as alleviating clinical EAE scores, inhibiting inflammation, and reducing demyelination in the CNS. SA also promoted the differentiation of OPCs as well as their remyelination after lysolecithin-induced demyelination. Furthermore, we showed that the promotion effect of SA on OPC differentiation was associated with the up-regulation of phosphorylated mTOR. Taken together, our results demonstrated that SA could act as a potential drug candidate for the treatment of demyelinating diseases.
引用
收藏
页码:434 / 446
页数:13
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