Glucagon-Like Peptide-1 Receptor Agonists as Potential Myelination-Inducible and Anti-Demyelinating Remedies

被引:13
|
作者
Sango, Kazunori [1 ]
Takaku, Shizuka [1 ]
Tsukamoto, Masami [1 ]
Niimi, Naoko [1 ]
Yako, Hideji [1 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Dis & Infect, Diabet Neuropathy Project, Tokyo, Tokyo, Japan
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2022年 / 10卷
关键词
glucagon-like peptide-1 receptor agonists; neuroprotection; axonal injury; diabetic neuropathy (DN); multiple sclerosis (MS); Schwann cells; olfactory ensheathing cells; oligodendrocytes; EXENDIN-4; INSULIN; CELLS; NEUROPROTECTION; LIRAGLUTIDE; ACTIVATION; MECHANISMS; EXENATIDE; MIGRATION; PATHWAYS;
D O I
10.3389/fcell.2022.950623
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucagon-like peptide-1 receptor agonists (GLP-1RAs) were developed as insulinotropic and anti-hyperglycemic agents for the treatment of type 2 diabetes, but their neurotrophic and neuroprotective activities have been receiving increasing attention. Myelin plays a key role in the functional maintenance of the central and peripheral nervous systems, and recent in vivo and in vitro studies have shed light on the beneficial effects of GLP-1RAs on the formation and protection of myelin. In this article, we describe the potential efficacy of GLP-1RAs for the induction of axonal regeneration and remyelination following nerve lesions and the prevention and alleviation of demyelinating disorders, particularly multiple sclerosis.
引用
收藏
页数:7
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