Flavonoids from Seabuckthorn (Hippophae rhamnoides L.) mimic neurotrophic functions in inducing neurite outgrowth in cultured neurons: Signaling via PI3K/Akt and ERK pathways

被引:11
|
作者
Xia, Chen-Xi [1 ,2 ,3 ]
Gao, Alex Xiong [1 ,2 ,3 ]
Dong, Tina Ting-Xia [1 ,2 ,3 ]
Tsim, Karl Wah-Keung [1 ,2 ,3 ]
机构
[1] HKUST Shenzhen Res Inst, Shenzhen Key Lab Edible & Med Bioresources, Hitech Pk, Shenzhen 518000, Peoples R China
[2] Hong Kong Univ Sci & Technol, Div Life Sci, Clear Water Bay, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Ctr Chinese Med, Clear Water Bay, Hong Kong, Peoples R China
关键词
Hippophae rhamnoides L; Flavonoid; Neurite outgrowth; Neurodegenerative diseases; PC-12; CELLS; BIOAVAILABILITY; EXPRESSION;
D O I
10.1016/j.phymed.2023.154832
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Various brain disorders, including neurodegenerative diseases and major depressive disorders, threaten an increasing number of patients. Seabuckthorn, a fruit from Hippophae rhamnoides L., is an example of "medicine food homology". The fruit has enriched flavonoids that reported to have benefits in treating cognitive disorders. However, the studies on potential functions of Seabuckthorn and/or its flavonoid-enriched fraction in treating neurodegenerative disorders are limited. Purpose: This study aimed to determine the ability and mechanism of the flavonoid-enriched fraction of Sea-buckthorn (named as SBF) in mimicking the neurotrophic functions in inducing neurite outgrowth of cultured neurons. Methods: Cultured PC12 cell line, SH-SY5Y cell line and primary neurons (cortical and hippocampal neurons isolated from E17-19 SD rat embryos) were the employed models to evaluate SBF in inducing neurite outgrowth by comparing to the effects of NGF and BDNF. Immuno-fluorescence staining was applied to identify the morphological change during the neuronal differentiation. Luciferase assay was utilized for analyzing the transcriptional regulation of neurofilaments and cAMP/CREB-mediated gene. Western blot assay was conducted to demonstrate the expressions of neurofilaments and phosphorylated proteins. Results: The application of SBF induced neuronal cell differentiation, and this differentiating activation was blocked by the inhibitors of PI3K/Akt and ERK pathways. Additionally, SBF showed synergy with neurotrophic factors in stimulating the neurite outgrowth of cultured neurons. Moreover, the major flavonoids within SBF, i.e., isorhamnetin, quercetin and kaempferol, could account for the neurotrophic activities of SBF. Conclusion: Seabuckthorn flavonoids mimicked neurotrophic functions in inducing neuronal cell differentiation via activating PI3K/Akt and ERK pathways. The results suggest the beneficial functions of Seabuckthorn as a potential health food supplement in treating various brain disorders, e.g., neurodegenerative diseases.
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页数:10
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