Mechanisms of Short-Chain Fatty Acids Derived from Gut Microbiota in Alzheimer's Disease

被引:86
作者
Qian, Xiao-hang [1 ,2 ]
Xie, Ru-yan [3 ]
Liu, Xiao-li [4 ]
Chen, Sheng-di [1 ,2 ]
Tang, Hui-dong [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Rui Jin Hosp, Sch Med, Dept Neurol, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Rui Jin Hosp, Sch Med, Inst Neurol, Shanghai 200025, Peoples R China
[3] Shanghai Guangci Mem Hosp, Shanghai 200025, Peoples R China
[4] Shanghai Jiao Tong Univ Affiliated Peoples Hosp 6, Dept Neurol, Shanghai Fengxian Dist Cent Hosp, South Campus, Shanghai 201406, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; gut microbiota; short-chain fatty acids; PROTEIN-COUPLED RECEPTOR; INULIN-TYPE FRUCTANS; HISTONE DEACETYLASES; MOUSE MODEL; FUNCTIONAL-CHARACTERIZATION; INTESTINAL MICROBIOTA; EPIGENETIC MECHANISMS; INTERNATIONAL UNION; SIGNALING PATHWAY; NERVOUS-SYSTEM;
D O I
10.14336/AD.2021.1215
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Short-chain fatty acids (SCFAs) are important metabolites derived from the gut microbiota through fermentation of dietary fiber. SCFAs participate a number of physiological and pathological processes in the human body, such as host metabolism, immune regulation, appetite regulation. Recent studies on gut-brain interaction have shown that SCFAs are important mediators of gut-brain interactions and are involved in the occurrence and development of many neurodegenerative diseases, including Alzheimer's disease. This review summarizes the current research on the potential roles and mechanisms of SCFAs in AD. First, we introduce the metabolic distribution, specific receptors and signaling pathways of SCFAs in human body. The concentration levels of SCFAs in AD patient/animal models are then summarized. In addition, we illustrate the effects and mechanisms of SCFAs on the cognitive level, pathological features (A ss and tau) and neuroinflammation in AD. Finally, we analyze the translational value of SCFAs as potential therapeutic targets for the treatment of AD.
引用
收藏
页码:1252 / 1266
页数:15
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