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水仙苷通过增强MiR200a/Nrf-2/GSH轴及介导MAPK/Akt相关信号通路对6-羟基多巴胺诱导的帕金森病模型的神经保护作用

Neuroprotective Capability of Narcissoside in 6-OHDA-Exposed Parkinson's Disease Models through Enhancing the MiR200a/Nrf-2/GSH Axis and Mediating MAPK/Akt Associated Signaling Pathway.

作者信息

Fu Ru-Huei, Tsai Chia-Wen, Liu Shih-Ping, Chiu Shao-Chih, Chen Yen-Chuan, Chiang Yu-Ting, Kuo Yun-Hua, Shyu Woei-Cherng, Lin Shinn-Zong

机构信息

Graduate Institute of Biomedical Sciences, China Medical University, Taichung 40402, Taiwan.

Translational Medicine Research Center, China Medical University Hospital, Taichung 40447, Taiwan.

出版信息

Antioxidants (Basel). 2022 Oct 23;11(11):2089. doi: 10.3390/antiox11112089.

DOI:10.3390/antiox11112089
PMID:36358461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9686521/
Abstract

We assessed the antioxidant potential of narcissoside from flowers (elderflowers) in Parkinson's disease models in vitro and in vivo. The results showed that narcissoside lessened the 6-hydroxydopamine (6-OHDA)-induced increase in reactive oxygen species (ROS) and apoptosis in SH-SY5Y cells. In the 6-OHDA-exposed model, narcissoside reduced degeneration of dopaminergic neurons and ROS generation, and also improved dopamine-related food-sensitive behavior and shortened lifespan. Moreover, NCS increased total glutathione (GSH) by increasing the expression of the catalytic subunit and modifier subunit of γ-glutamylcysteine ligase in cells and nematodes. Treatment with a GSH inhibitor partially abolished the anti-apoptotic ability of narcissoside. Furthermore, narcissoside diminished the 6-OHDA-induced phosphorylation of JNK and p38, while rising activities of ERK and Akt in resisting apoptosis. The antioxidant response element (ARE)-luciferase reporter activity analysis and electromobility gel shift assay showed that narcissoside promotes the transcriptional activity mediated by Nrf2. Finally, we found that narcissoside augmented the expression of miR200a, a translational inhibitor of the Nrf2 repressor protein Keap1. Downregulation of Nrf2 and miR200a by RNAi and anti-miR200a, respectively, reversed the neuroprotective ability of narcissoside. In summary, narcissoside can enhance the miR200a/Nrf2/GSH antioxidant pathway, alleviate 6-OHDA-induced apoptosis, and has the neuroprotective potential.

摘要

我们在体外和体内帕金森病模型中评估了来自花朵(接骨木花)的水仙苷的抗氧化潜力。结果表明,水仙苷减轻了6-羟基多巴胺(6-OHDA)诱导的SH-SY5Y细胞中活性氧(ROS)增加和细胞凋亡。在6-OHDA暴露模型中,水仙苷减少了多巴胺能神经元的退化和ROS生成,还改善了与多巴胺相关的食物敏感行为并缩短了寿命。此外,水仙苷通过增加细胞和线虫中γ-谷氨酰半胱氨酸连接酶催化亚基和修饰亚基的表达来增加总谷胱甘肽(GSH)。用GSH抑制剂处理部分消除了水仙苷的抗凋亡能力。此外,水仙苷减少了6-OHDA诱导的JNK和p38磷酸化,同时提高了ERK和Akt在抵抗细胞凋亡中的活性。抗氧化反应元件(ARE)-荧光素酶报告基因活性分析和电泳迁移率凝胶阻滞试验表明,水仙苷促进了由Nrf2介导的转录活性。最后,我们发现水仙苷增加了miR200a的表达,miR200a是Nrf2抑制蛋白Keap1的翻译抑制剂。分别通过RNAi和抗miR200a下调Nrf2和miR200a可逆转水仙苷的神经保护能力。总之,水仙苷可增强miR200a/Nrf2/GSH抗氧化途径,减轻6-OHDA诱导的细胞凋亡,具有神经保护潜力。

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