Neuroprotective Effects of Icariin on Brain Metabolism, Mitochondrial Functions, and Cognition in Triple-Transgenic Alzheimer's Disease Mice

被引:106
作者
Chen, Yi-Jing [1 ]
Zheng, Hai-Yang [1 ]
Huang, Xiu-Xian [2 ]
Han, Shuang-Xue [1 ]
Zhang, Dong-Sheng [2 ]
Ni, Jia-Zuan [1 ]
He, Xiao-Yang [1 ]
机构
[1] Shenzhen Univ, Coll Life Sci, Shenzhen Key Lab Marine Bioresources & Ecol, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Life Sci, Shenzhen Key Lab Microbial Genet Engn, Shenzhen 518060, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Alzheimer's disease; Icariin; Magnetic resonance spectroscopy; Mitochondrial dysfunction; N-acetylaspartate; MAGNETIC-RESONANCE-SPECTROSCOPY; A-BETA; N-ACETYLASPARTATE; AMYLOID-BETA; MEMORY IMPAIRMENT; MOUSE MODEL; WATER-MAZE; H-1; MRS; DEFICITS; DYSFUNCTION;
D O I
10.1111/cns.12473
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Aims: This study investigated the neuroprotective properties of icariin (an effective component of traditional Chinese herbal medicine Epimedium) on neuronal function and brain energy metabolism maintenance in a triple-transgenic mouse model of Alzheimer's disease (3 9 Tg-AD). Methods: 3 9 Tg-AD mice as well as primary neurons were subjected to icariin treatment. Morris water maze assay, magnetic resonance spectroscopy (MRS), Western blotting, ELISA, and immunohistochemistry analysis were used to evaluate the effects of icariin administration. Results: Icariin significantly improved spatial learning and memory retention in 3 9 Tg-AD mice, promoted neuronal cell activity as identified by the enhancement of brain metabolite N-acetylaspartate level and ATP production in AD mice, preserved the expressions of mitochondrial key enzymes COX IV, PDHE1 alpha, and synaptic protein PSD95, reduced A beta plaque deposition in the cortex and hippocampus of AD mice, and inhibited beta-site APP cleavage enzyme 1 (BACE1) expression. Icariin treatment also decreased the levels of extracellular and intracellular A beta 1-42 in 3 9 Tg-AD primary neurons, modulated the distribution of A beta along the neurites, and protected against mitochondrial fragmentation in 3 9 Tg-AD neurons. Conclusions: Icariin shows neuroprotective effects in 3 9 Tg-AD mice and may be a promising multitarget drug in the prevention/protection against AD.
引用
收藏
页码:63 / 73
页数:11
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