Protective roles of Amanita caesarea polysaccharides against Alzheimer's disease via Nrf2 pathway

被引:54
|
作者
Li, Zhiping [1 ]
Chen, Xia [1 ]
Zhang, Yongfeng [2 ]
Liu, Xin [2 ]
Wang, Chunyue [2 ]
Teng, Lesheng [2 ]
Wang, Di [2 ]
机构
[1] Jilin Univ, Coll Basic Med Sci, Dept Pharmacol, Changchun 130006, Jilin, Peoples R China
[2] Jilin Univ, Sch Life Sci, Changchun, Jilin, Peoples R China
关键词
A. caesarea polysaccharides; Alzheimer's disease; Nrf2; pathway; AMYLOID-BETA-PEPTIDE; OXIDATIVE STRESS; MECHANISMS; HEALTH; DEATH; MICE; BAX;
D O I
10.1016/j.ijbiomac.2018.09.216
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
This study explores the neuro-protective effects of Amanita caesarea polysaccharides (ACPS), obtained by 80% alcohol precipitation of water extract and purified using a DEAE-52 cellulose anion exchange column, related to antioxidant activity. A 3-h pre-treatment of ACPS prior to L-glutamic acid (L-Glu) co-exposure reversed the decreased cell viability, inhibited apoptosis, suppressed the accumulation of intracellular reactive oxygen species and restored mitochondrial membrane potential in HT22 cells. Compared to L-Glu-exposed cells, ACPS enhanced the nuclear levels of NF-E2p45-related factor 2 (Nrf2), reduced the cytoplasmic levels of Nrf2 and cytochrome C, suppressed the expression of Kelch-like ECH-associated protein 1, and enhanced the expression of heme oxygen-ase-1, superoxide dismutase 1 and cysteine ligase catalytic subunit. In a D-galactose and aluminum trichloride Alzheimer's disease (AD) mouse model, 42-day administration of ACPS improved the abnormal behaviors. ACPS suppressed the deposition of beta-amyloid peptide in the brain and ameliorated oxidative stress via modulating the levels of related enzymes. ACPS improved the functioning of the central cholinergic system, as indicated by an increase in acetylcholine and choline acetyltransferase concentrations, and reduced acetylcholine esterase levels in the serum, hypothalamus and cerebral cortex. Our data suggest that ACPS may be a promising candidate for the treatment of AD. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:29 / 37
页数:9
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