Magnesium-L-threonate treats Alzheimer's disease by modulating the microbiota-gut-brain axis

被引:0
作者
Wang Liao [1 ]
Jiana Wei [1 ,2 ]
Chongxu Liu [1 ]
Haoyu Luo [1 ]
Yuting Ruan [3 ]
Yingren Mai [1 ]
Qun Yu [4 ]
Zhiyu Cao [4 ]
Jiaxin Xu [4 ]
Dong Zheng [5 ]
Zonghai Sheng [6 ]
Xianju Zhou [2 ]
Jun Liu [1 ]
机构
[1] Department of Neurology,The Second Affiliated Hospital of Guangzhou Medical University
[2] Special Medical Service Center,Neuroscience Center,Integrated Hospital of Traditional Chinese Medicine,Southern Medical University
[3] Department of Rehabilitation,The Second Affiliated Hospital,Guangzhou Medical University
[4] Department of Neurology,Sun Yat-sen Memorial Hospital,Sun Yat-sen University
[5] Department of Neurology,The Affiliated Brain Hospital of Guangzhou Medical University
[6] Institute of Biomedical and Health Engineering,Shenzhen Institute of Advanced Technology,Chinese Academy of Sciences
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
R749.16 [];
学科分类号
100203 ;
摘要
Disturbances in the microbiota-gut-brain axis may contribute to the development of Alzheimer’s disease. Magnesium-L-threonate has recently been found to have protective effects on learning and memory in aged and Alzheimer’s disease model mice. However, the effects of magnesium-L-threonate on the gut microbiota in Alzheimer’s disease remain unknown. Previously, we reported that magnesium-L-threonate treatment improved cognition and reduced oxidative stress and inflammation in a double-transgenic line of Alzheimer’s disease model mice expressing the amyloid-β precursor protein and mutant human presenilin 1(APP/PS1). Here, we performed 16S r RNA amplicon sequencing and liquid chromatography-mass spectrometry to analyze changes in the microbiome and serum metabolome following magnesium-Lthreonate exposure in a similar mouse model. Magnesium-L-threonate modulated the abundance of three genera in the gut microbiota, decreasing Allobaculum and increasing Bifidobacterium and Turicibacter. We also found that differential metabolites in the magnesiumL-threonate-regulated serum were enriched in various pathways associated with neurodegenerative diseases. The western blotting detection on intestinal tight junction proteins(zona occludens 1, occludin, and claudin-5) showed that magnesium-L-threonate repaired the intestinal barrier dysfunction of APP/PS1 mice. These findings suggest that magnesium-L-threonate may reduce the clinical manifestations of Alzheimer’s disease through the microbiota-gut-brain axis in model mice, providing an experimental basis for the clinical treatment of Alzheimer’s disease.
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页码:2281 / 2289
页数:9
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