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Published on: June 2, 2022
Dynamic dual roles of gut microbial metabolites in Alzheimer's disease: Translational insights for gut-brain axis
Xutao Ye1, Xiaodong Jing1, Zhongyuan Li1
1Key Laboratory of Industrial Fermentation Microbiology of the Ministry of Education and Tianjin Key Laboratory of Industrial Microbiology, College of Biotechnology, Tianjin University of Science and Technology, Tianjin 300457, China; National Demonstration Center for Experimental Bioengineering Education, Tianjin University of Science and Technology, Tianjin 300457, China.
Abstract:
Alzheimer's disease (AD) is a complex neurodegenerative disorder in which the microbiome-gut-brain axis (MGBA) plays a crucial regulatory role through microbial metabolites. This review analyzes the concentration trajectories of representative metabolites across different disease stages and compartments, and synthesizes current preclinical evidence on how these metabolites influence AD pathogenesis, with particular attention to the mechanisms underlying their dual roles. We integrate evidence for bidirectional pathological crosstalk: gut dysbiosis accelerates central neurodegeneration through altered metabolite signaling, while AD-related neuropathology concurrently disrupts gut homeostasis. The review also evaluates MGBA-targeted intervention strategies and critically identifies key limitations that hinder clinical translation, including unclear dose-response relationships and insufficient patient stratification. We note that brain-to-gut mechanistic evidence remains considerably less developed than that for the gut-to-brain direction, and that signaling crosstalk among multiple metabolites is poorly characterized. Future studies should prioritize the neuroendocrine and immune pathways linking central pathology to gut dysbiosis, the dose-response relationships of individual metabolites, and standardized multi-metabolite profiling within prospective longitudinal cohorts. Addressing these gaps will advance mechanism-guided, precision-targeted interventions that mitigate the prevalent gut dysfunction in AD and confer global therapeutic benefits.
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