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Published on: December 26, 2016
The Microbiota-Gut-Brain Axis and Alzheimer's Disease: Neuroinflammation Is to Blame?
Ashwinipriyadarshini Megur1, Daiva Baltriukienė1, Virginija Bukelskienė1
1Life Sciences Center, Department of Biological Models, Institute of Biochemistry, Vilnius University, Sauletekio Ave. 7, LT-10257 Vilnius, Lithuania.
Abstract:
For years, it has been reported that Alzheimer's disease (AD) is the most common cause of dementia. Various external and internal factors may contribute to the early onset of AD. This review highlights a contribution of the disturbances in the microbiota-gut-brain (MGB) axis to the development of AD. Alteration in the gut microbiota composition is determined by increase in the permeability of the gut barrier and immune cell activation, leading to impairment in the blood-brain barrier function that promotes neuroinflammation, neuronal loss, neural injury, and ultimately AD. Numerous studies have shown that the gut microbiota plays a crucial role in brain function and changes in the behavior of individuals and the formation of bacterial amyloids. Lipopolysaccharides and bacterial amyloids synthesized by the gut microbiota can trigger the immune cells residing in the brain and can activate the immune response leading to neuroinflammation. Growing experimental and clinical data indicate the prominent role of gut dysbiosis and microbiota-host interactions in AD. Modulation of the gut microbiota with antibiotics or probiotic supplementation may create new preventive and therapeutic options in AD. Accumulating evidences affirm that research on MGB involvement in AD is necessary for new treatment targets and therapies for AD.
Insights
Disturbances in the microbiota-gut-brain axis contribute to Alzheimer's disease (AD) development. Modulating gut microbiota may offer new therapeutic strategies for AD.
Area of Science:
- Neuroscience
- Microbiology
- Gastroenterology
Background:
- Alzheimer's disease (AD) is a leading cause of dementia.
- The microbiota-gut-brain (MGB) axis plays a role in brain function and behavior.
Purpose of the Study:
- To review the contribution of MGB axis disturbances to AD development.
- To highlight the role of gut dysbiosis in AD pathogenesis.
Main Methods:
- Review of experimental and clinical data on the MGB axis and AD.
- Analysis of the impact of gut microbiota alterations on the blood-brain barrier and neuroinflammation.
Main Results:
- Gut microbiota alterations increase gut permeability and activate immune cells, impairing blood-brain barrier function.
- Bacterial products like lipopolysaccharides and amyloids trigger neuroinflammation, neuronal loss, and injury.
- Gut dysbiosis and microbiota-host interactions are implicated in AD.
Conclusions:
- The MGB axis is a significant factor in AD development.
- Modulating gut microbiota through antibiotics or probiotics presents potential preventive and therapeutic avenues for AD.
- Further research into MGB axis involvement is crucial for identifying new AD treatment targets.
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