Microbiome Alterations and Alzheimer's Disease: Modeling Strategies with Transgenic Mice.
Alzheimer’s disease
amyloid
dysbiosis
fecal microbiota transplantation
metabolic diseases
microbiota
neuroinflammation
probiotics
tau
transgenic mouse models
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
27 Jun 2023
27 Jun 2023
Historique:
received:
07
06
2023
revised:
21
06
2023
accepted:
23
06
2023
medline:
29
7
2023
pubmed:
29
7
2023
entrez:
29
7
2023
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 37509487
pii: biomedicines11071846
doi: 10.3390/biomedicines11071846
pmc: PMC10377071
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Subventions
Organisme : University of Malaga
ID : C1 from Plan Propio
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