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热量限制可促进多发性硬化症的 Cuprizone 诱导脱髓鞘模型中的髓鞘再生。

Calorie restriction promotes remyelination in a Cuprizone-Induced demyelination mouse model of multiple sclerosis.

机构信息

Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Department of Anatomy, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.

出版信息

Metab Brain Dis. 2020 Oct;35(7):1211-1224. doi: 10.1007/s11011-020-00597-0. Epub 2020 Jul 7.

DOI:10.1007/s11011-020-00597-0
PMID:32638202
Abstract

Over the past few decades several attempts have been made to introduce a potential and promising therapy for Multiple sclerosis (MS). Calorie restriction (CR) is a dietary manipulation to reduce calorie intake which has been shown to improve neuroprotection and attenuate neurodegenerative disorders. Here, we evaluated the effect of 33% CR regimen for 4 weeks on the remyelination capacity of Cuprizone (CPZ) induced demyelination in a mouse model of MS. Results showed that CR induced a significant increase in motor coordination and balance performance in CPZ mice. Also, luxol fast blue (LFB) staining showed that CR regimen significantly improved the remyelination in the corpus callosum of CPZ + CR mice compared to the CPZ group. In addition, CR regimen significantly increased the transcript expression levels of BDNF, Sox2, and Sirt1 in the corpus callosum of CPZ mice, while decreasing the p53 levels. Moreover, CR regimen significantly decreased the apoptosis rate. Furthermore, astrogliosis (GFAP + astrocytes) and microgliosis (Iba-1 + microglia) were significantly decreased by CR regimen while oligodendrogenesis (Olig2+) and Sirt1 + cell expression were significantly increased in the corpus callosum of CPZ + CR mice compared to the CPZ group. In conclusion, CR regimen can promote remyelination potential in a CPZ-demyelinating mouse model of MS by increasing oligodendrocyte generation while decreasing their apoptosis.

摘要

在过去的几十年中,人们曾多次尝试为多发性硬化症 (MS) 引入一种有潜力和前景的治疗方法。热量限制 (CR) 是一种减少热量摄入的饮食干预措施,已被证明可改善神经保护并减轻神经退行性疾病。在这里,我们评估了为期 4 周的 33% CR 方案对 CPZ 诱导的 MS 小鼠模型脱髓鞘的髓鞘再生能力的影响。结果表明,CR 方案可显著提高 CPZ 小鼠的运动协调和平衡能力。此外,卢索快速蓝 (LFB) 染色显示,与 CPZ 组相比,CR 方案可显著改善 CPZ+CR 小鼠胼胝体的髓鞘再生。此外,CR 方案可显著增加 CPZ 小鼠胼胝体中 BDNF、Sox2 和 Sirt1 的转录表达水平,同时降低 p53 水平。此外,CR 方案还可显著降低细胞凋亡率。此外,星形胶质细胞增生 (GFAP+星形胶质细胞) 和小胶质细胞增生 (Iba-1+小胶质细胞) 可被 CR 方案显著减少,而少突胶质细胞生成 (Olig2+) 和 Sirt1+细胞表达在 CPZ+CR 小鼠的胼胝体中明显增加,与 CPZ 组相比。总之,CR 方案可通过增加少突胶质细胞的生成并减少其凋亡来促进 CPZ 脱髓鞘 MS 小鼠模型的髓鞘再生潜能。

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