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Updated: Jun 11, 2026

Quantitative 3D In Silico Modeling (q3DISM) of Cerebral Amyloid-beta Phagocytosis in Rodent Models of Alzheimer's Disease
Published on: December 26, 2016
Gut microbiota in Alzheimer's disease: Understanding molecular pathways and potential therapeutic perspectives
Simone Lista1, Antonio Munafò2, Filippo Caraci3
1i+HeALTH Strategic Research Group, Department of Health Sciences, Miguel de Cervantes European University (UEMC), Valladolid 47012, Spain.
Abstract:
Accumulating evidence suggests that gut microbiota (GM) plays a crucial role in Alzheimer's disease (AD) pathogenesis and progression. This narrative review explores the complex interplay between GM, the immune system, and the central nervous system in AD. We discuss mechanisms through which GM dysbiosis can compromise intestinal barrier integrity, enabling pro-inflammatory molecules and metabolites to enter systemic circulation and the brain, potentially contributing to AD hallmarks. Additionally, we examine other pathophysiological mechanisms by which GM may influence AD risk, including the production of short-chain fatty acids, secondary bile acids, and tryptophan metabolites. The role of the vagus nerve in gut-brain communication is also addressed. We highlight potential therapeutic implications of targeting GM in AD, focusing on antibiotics, probiotics, prebiotics, postbiotics, phytochemicals, and fecal microbiota transplantation. While preclinical studies showed promise, clinical evidence remains limited and inconsistent. We critically assess clinical trials, emphasizing challenges in translating GM-based therapies to AD patients. The reviewed evidence underscores the need for further research to elucidate precise molecular mechanisms linking GM to AD and determine whether GM dysbiosis is a contributing factor or consequence of AD pathology. Future studies should focus on large-scale clinical trials to validate GM-based interventions' efficacy and safety in AD.
Insights
Gut microbiota (GM) influences Alzheimer's disease (AD) by affecting the gut-brain axis. While therapies targeting GM show promise, clinical evidence for treating AD is limited and requires further investigation.
Area of Science:
- Neuroscience
- Microbiology
- Immunology
Background:
- Gut microbiota (GM) is increasingly implicated in Alzheimer's disease (AD) pathogenesis.
- Dysbiosis of GM may compromise intestinal integrity, leading to neuroinflammation and AD hallmarks.
Purpose of the Study:
- To review the intricate relationship between GM, immunity, and the central nervous system in AD.
- To explore mechanisms linking GM to AD and evaluate therapeutic strategies targeting GM.
Main Methods:
- Narrative review of existing literature.
- Analysis of preclinical and clinical studies on GM-based interventions for AD.
Main Results:
- GM dysbiosis can promote inflammation and influence AD through various metabolites and the vagus nerve.
- Preclinical studies show therapeutic potential, but clinical evidence for interventions like probiotics and FMT is inconsistent.
Conclusions:
- Further research is needed to clarify the precise role of GM in AD etiology and progression.
- Large-scale clinical trials are essential to validate the efficacy and safety of GM-based therapies for Alzheimer's disease.
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