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芝麻素通过ERK1/2通路和SIRT1调节在神经生长因子不足条件下促进PC12细胞的神经突生长。

Sesamin Promotes Neurite Outgrowth under Insufficient Nerve Growth Factor Condition in PC12 Cells through ERK1/2 Pathway and SIRT1 Modulation.

作者信息

Udomruk Sasimol, Kaewmool Chayanut, Phitak Thanyaluck, Pothacharoen Peraphan, Kongtawelert Prachya

机构信息

Thailand Excellence Center for Tissue Engineering and Stem Cells, Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Evid Based Complement Alternat Med. 2020 Mar 26;2020:9145458. doi: 10.1155/2020/9145458. eCollection 2020.

DOI:10.1155/2020/9145458
PMID:32308720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7139881/
Abstract

The promotion of neurogenesis can be a promising strategy to improve and restore neuronal function in neurodegenerative diseases. Nerve growth factor (NGF) plays a key role in neurite outgrowth and synaptic formation during brain repair stage. Nowadays, there are several studies on the developing methods to enhance the endogenous NGF activity for treatment and restore the neuronal function. In this study, the potentiating effect of sesamin, a major lignan in sesame seeds () and oil, on NGF-induced neurogenesis and its involved mechanisms were firstly reported. Sesamin effectively enhanced the PC12 neuron-like cell differentiation and neurite length under insufficient conditions of NGF. The neuronal markers including synaptophysin and growth-associated protein-43 along with the synaptic connections were significantly increased in combination treatment between sesamin and NGF. Moreover, sesamin also increased the level of phospho-ERK1/2 and SIRT1 protein, an important regulatory protein of the neurogenesis process. The neurogenesis was blocked by the specific SIRT1 inhibitor, JGB1741, suggesting that the neuritogenic effect of sesamin was associated with SIRT1 protein modulation. Taken together, the potentiating effect of sesamin on NGF-induced neurogenesis in this finding could be used for alternative treatment in neurodegenerative diseases, including Alzheimer's disease.

摘要

促进神经发生可能是改善和恢复神经退行性疾病中神经元功能的一种有前景的策略。神经生长因子(NGF)在脑修复阶段的神经突生长和突触形成中起关键作用。如今,有几项关于开发增强内源性NGF活性以治疗和恢复神经元功能的方法的研究。在本研究中,首次报道了芝麻素(芝麻籽及其油中的一种主要木脂素)对NGF诱导的神经发生的增强作用及其相关机制。在NGF不足的条件下,芝麻素有效地增强了PC12神经元样细胞的分化和神经突长度。在芝麻素和NGF联合处理中,包括突触素和生长相关蛋白43在内的神经元标志物以及突触连接显著增加。此外,芝麻素还增加了磷酸化ERK1/2和SIRT1蛋白的水平,SIRT1蛋白是神经发生过程中的一种重要调节蛋白。神经发生被特异性SIRT1抑制剂JGB1741阻断,这表明芝麻素的促神经突生长作用与SIRT1蛋白调节有关。综上所述,本研究中芝麻素对NGF诱导的神经发生的增强作用可用于神经退行性疾病(包括阿尔茨海默病) 的替代治疗。

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