Harnessing the power of ginger leaf polysaccharide: A potential strategy to combat A(3-induced toxicity through the Wnt/(3-catenin pathway

被引:0
|
作者
Zhang, Zhong-hao [1 ]
Pei, Ying-hong [1 ]
Duan, Zhi-hao [1 ]
Gao, Tao [1 ]
Feng, Shi-ling [1 ]
Tang, Zi-zhong [1 ]
Chen, Yang-er [1 ]
Hu, Sheng-lin [2 ]
Yuan, Shu [3 ]
Wang, Wei [4 ]
Yan, Xiao-rong [2 ]
Pu, Ya-ying [2 ]
Yuan, Ming [1 ]
机构
[1] Sichuan Agr Univ, Coll Life Sci, Yaan 625014, Sichuan Provinc, Peoples R China
[2] Yaan Peoples Hosp, Yaan 625099, Peoples R China
[3] Sichuan Agr Univ, Coll Resources, Chengdu 611130, Sichuan Provinc, Peoples R China
[4] Dazhu Cty Sci & Technol Informat Res Inst, Chengdu 635000, Sichuan Provinc, Peoples R China
关键词
Ginger leaf polysaccharide; Alzheimer's disease; A(3; Wnt/(3-catenin pathway; Neurotoxicity; AMYLOID-BETA PEPTIDE; ALZHEIMERS-DISEASE; CAENORHABDITIS-ELEGANS; COGNITIVE FUNCTION; MOUSE MODEL; A-BETA; IMPAIRMENT; MECHANISM; PATHOLOGY;
D O I
10.1016/j.ijbiomac.2025.140692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is prevalent in the elderly, with amyloid-(3 (A(3) playing a critical role in its progression. Polysaccharides have garnered increasing attention due to their low toxicity and diverse applications in alleviating AD-like symptoms. However, the potential of ginger leaf polysaccharide in mitigating AD-like symptoms has been rarely investigated. In this study, we isolated a polysaccharide (GLP1) from ginger leaf and evaluated its efficacy and underlying mechanisms in alleviating AD-like symptoms using Caenorhabditis elegans and PC12 cells. GLP1 ameliorated AD-like symptoms in C. elegans, as evidenced by a 41.50 % increase in head thrashing frequency and an 87.13 % increase in body bending frequency. Furthermore, GLP1 mitigated cognitive decline by 76.51 %. Additionally, GLP1 enhanced the activity of acetylcholinesterase in C. elegans and maintained the integrity of neural system function. Moreover, GLP1 improved the survival rate of PC12 cells under A(3 induction by activating the Wnt/(3-catenin pathway, which also resulted in a reduction in the release of inflammatory factors, specifically IL-1(3 by 21.15 %, IL-6 by 39.98 %, and TNF-alpha by 19.66 %. Notably, FITC-labeled GLP1 could be absorbed by PC12 cells. These compelling findings underscored the therapeutic potential of GLP1 in alleviating A(3-induced AD-like symptoms and supported the advancement of ginger leaf resource utilization.
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页数:14
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