Microbiome Alterations and Alzheimer's Disease: Modeling Strategies with Transgenic Mice.
Juan Antonio López-VillodresAlejandro EscamillaSilvia Mercado-SáenzCarmen Alba-TercedorLuis Manuel Rodriguez-PerezIsabel Arranz-SalasRaquel Sanchez-VaroDiego BermúdezPublished in: Biomedicines (2023)
In the last decade, the role of the microbiota-gut-brain axis has been gaining momentum in the context of many neurodegenerative and metabolic disorders, including Alzheimer's disease (AD) and diabetes, respectively. Notably, a balanced gut microbiota contributes to the epithelial intestinal barrier maintenance, modulates the host immune system, and releases neurotransmitters and/or neuroprotective short-chain fatty acids. However, dysbiosis may provoke immune dysregulation, impacting neuroinflammation through peripheral-central immune communication. Moreover, lipopolysaccharide or detrimental microbial end-products can cross the blood-brain barrier and induce or at least potentiate the neuropathological progression of AD. Thus, after repeated failure to find a cure for this dementia, a necessary paradigmatic shift towards considering AD as a systemic disorder has occurred. Here, we present an overview of the use of germ-free and/or transgenic animal models as valid tools to unravel the connection between dysbiosis, metabolic diseases, and AD, and to investigate novel therapeutical targets. Given the high impact of dietary habits, not only on the microbiota but also on other well-established AD risk factors such as diabetes or obesity, consistent changes of lifestyle along with microbiome-based therapies should be considered as complementary approaches.
Keyphrases
- type diabetes
- cardiovascular disease
- risk factors
- metabolic syndrome
- weight loss
- fatty acid
- cognitive decline
- cerebral ischemia
- glycemic control
- mild cognitive impairment
- cognitive impairment
- traumatic brain injury
- insulin resistance
- lps induced
- microbial community
- toll like receptor
- physical activity
- white matter
- lipopolysaccharide induced
- body mass index
- immune response
- chemotherapy induced