GLP-1/Sigma/RAGE receptors: An evolving picture of Alzheimer's disease pathology and treatment.
AD
AGE
GLP-1
Neuroprotection
RAGE
Sigma-1R
Sigma-2R
Journal
Ageing research reviews
ISSN: 1872-9649
Titre abrégé: Ageing Res Rev
Pays: England
ID NLM: 101128963
Informations de publication
Date de publication:
25 Nov 2023
25 Nov 2023
Historique:
received:
03
09
2023
revised:
18
11
2023
accepted:
19
11
2023
pubmed:
27
11
2023
medline:
27
11
2023
entrez:
26
11
2023
Statut:
aheadofprint
Résumé
According to the facts and figures 2023stated that 6.7 million Americans over the age of 65 have Alzheimer's disease (AD). The scenario of AD has reached up to the maximum, of 4.1 million individuals, 2/3rd are female patients, and approximately 1 in 9 adults over the age of 65 have dementia with AD dementia. The fact that there are now no viable treatments for AD indicates that the underlying disease mechanisms are not fully understood. The progressive neurodegenerative disease, AD is characterized by amyloid plaques and neurofibrillary tangles (NFTs) of abnormally hyperphosphorylated tau protein and senile plaques (SPs), which are brought on by the buildup of amyloid beta (Aβ). Numerous attempts have been made to produce compounds that interfere with these characteristics because of significant research efforts into the primary pathogenic hallmark of this disorder. Here, we summarize several research that highlights interesting therapy strategies and the neuroprotective effects of GLP-1, Sigma, and, AGE-RAGE receptors in pre-clinical and clinical AD models.
Identifiants
pubmed: 38008402
pii: S1568-1637(23)00293-3
doi: 10.1016/j.arr.2023.102134
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
102134Informations de copyright
Copyright © 2023 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest There is no conflict of interest.