Nanowired delivery of cerebrolysin with neprilysin and p-Tau antibodies induces superior neuroprotection in Alzheimer's disease.
Alzheimer's disease
Antibodies
Blood-brain barrier
Brain edema
Brain pathology
Cerebrolysin
Nanowired delivery
Neurotrophic factors
Phosphorylated Tau protein
Journal
Progress in brain research
ISSN: 1875-7855
Titre abrégé: Prog Brain Res
Pays: Netherlands
ID NLM: 0376441
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
10
4
2019
pubmed:
10
4
2019
medline:
6
6
2019
Statut:
ppublish
Résumé
Alzheimer's disease (AD) is estimated to be afflicting over 55 millions of individual worldwide in 2018-19 for which no suitable clinical therapeutic measures have been developed so far. Thus, there is an urgent need to explore novel therapeutic strategies using nanodelivery of drugs and agents either alone or in combination for superior neuroprotection in AD and enhanced quality of life of the affected individuals. There are reports that AD is often associated with diminished neurotrophic factors and neprilysin together with enhancement of phosphorylated Tau (p-Tau) within the brain and in the cerebrospinal fluid (CSF). Thus, studies aiming to enhance neurotrophic factors and neprilysin together with neutralizing p-Tau within the central nervous system (CNS) may alleviate brain pathology in AD. In this review these strategies are discussed using nanotechnological approaches largely based on our own investigations in relation to current literature in the field.
Identifiants
pubmed: 30961867
pii: S0079-6123(19)30039-1
doi: 10.1016/bs.pbr.2019.03.009
pii:
doi:
Substances chimiques
Amino Acids
0
Antibodies
0
Neuroprotective Agents
0
tau Proteins
0
cerebrolysin
37KZM6S21G
Neprilysin
EC 3.4.24.11
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
145-200Subventions
Organisme : NIA NIH HHS
ID : R01 AG028679
Pays : United States
Informations de copyright
© 2019 Elsevier B.V. All rights reserved.