Nanowired Delivery of Cerebrolysin Together with Antibodies to Amyloid Beta Peptide, Phosphorylated Tau, and Tumor Necrosis Factor Alpha Induces Superior Neuroprotection in Alzheimer's Disease Brain Pathology Exacerbated by Sleep Deprivation.
Alzheimer’s disease
Brain pathology
Monoclonal antibodies
Nanomedicine amyloid beta peptide
Nanowired delivery
Neuroprotection
Phosphorylated p-tau
Serotonin6 receptor antagonist
Sleep deprivation
Journal
Advances in neurobiology
ISSN: 2190-5215
Titre abrégé: Adv Neurobiol
Pays: United States
ID NLM: 101571545
Informations de publication
Date de publication:
2023
2023
Historique:
medline:
24
7
2023
pubmed:
22
7
2023
entrez:
22
7
2023
Statut:
ppublish
Résumé
Sleep deprivation induces amyloid beta peptide and phosphorylated tau deposits in the brain and cerebrospinal fluid together with altered serotonin metabolism. Thus, it is likely that sleep deprivation is one of the predisposing factors in precipitating Alzheimer's disease (AD) brain pathology. Our previous studies indicate significant brain pathology following sleep deprivation or AD. Keeping these views in consideration in this review, nanodelivery of monoclonal antibodies to amyloid beta peptide (AβP), phosphorylated tau (p-tau), and tumor necrosis factor alpha (TNF-α) in sleep deprivation-induced AD is discussed based on our own investigations. Our results suggest that nanowired delivery of monoclonal antibodies to AβP with p-tau and TNF-α induces superior neuroprotection in AD caused by sleep deprivation, not reported earlier.
Identifiants
pubmed: 37480458
doi: 10.1007/978-3-031-32997-5_1
doi:
Substances chimiques
Amyloid beta-Peptides
0
Antibodies, Monoclonal
0
cerebrolysin
37KZM6S21G
Tumor Necrosis Factor-alpha
0
Nanoparticle Drug Delivery System
0
tau Proteins
0
Types de publication
Review
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3-53Informations de copyright
© 2023. The Author(s), under exclusive license to Springer Nature Switzerland AG.
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