| Literature DB >> 29036812 |
Ling Zhang1,2, Ying Wang1,2, Xia Xiayu1,2, Changhua Shi1,2, Wei Chen1,2, Nan Song1,2, Xinjing Fu1,2, Rui Zhou1,2, Yan-Feng Xu1,2, Lan Huang1,2, Hua Zhu1,2, Yunlin Han1,2, Chuan Qin1,2.
Abstract
The topic of gut microbiota is currently attracting considerable interest as a potential factor in Alzheimer's disease (AD). However, the extent and time course of alterations in the gut microbiota, and their effects on AD pathology remain uncertain. Herein, we compared the fecal microbiomes and fecal short chain fatty acid composition (SCFAs) between wild-type and AD model mice at different ages under strictly controlled specific pathogen free conditions, and also conducted microscopic investigations of intestinal structures. Our results showed that the microbiota composition and diversity were perturbed and the level of SCFAs was reduced in AD mice, predicting alterations in more than 30 metabolic pathways, which may be associated with amyloid deposition and ultrastructural abnormalities in AD mouse intestine. These findings indicate that AD pathology might not only affect brain function directly, but also exacerbate cognitive deficits through reducing the level of SCFAs via alterations of gut microbiota induced by intestinal amyloid deposition. Our data may support a role of gut microbiota, and suggest a novel route for therapeutic intervention in AD.Entities:
Keywords: Alzheimer’s disease; aging; gut microbiota; mouse model; short chain fatty acids
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Year: 2017 PMID: 29036812 DOI: 10.3233/JAD-170020
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472