Synthetic β-hydroxy ketone derivative inhibits cholinesterases, rescues oxidative stress and ameliorates cognitive deficits in 5XFAD mice model of AD.
Acetylcholinesterase
/ metabolism
Alzheimer Disease
/ drug therapy
Animals
Antioxidants
/ chemical synthesis
Butyrylcholinesterase
/ metabolism
Cholinesterase Inhibitors
/ chemical synthesis
Cognitive Dysfunction
/ enzymology
Cyclopentanes
/ chemical synthesis
Disease Models, Animal
Enzyme Assays
Frontal Lobe
/ drug effects
Hippocampus
/ drug effects
Ketones
/ chemical synthesis
Male
Maze Learning
/ drug effects
Mice
Mice, Transgenic
Neuroprotective Agents
/ chemical synthesis
Oxidative Stress
/ drug effects
Postural Balance
/ drug effects
Acetylcholine
Alzheimer’s disease
Antioxidant
Cholinesterase
Cognitive impairments
Neuroprotection
Journal
Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
20
08
2020
accepted:
11
11
2020
pubmed:
20
11
2020
medline:
20
5
2021
entrez:
19
11
2020
Statut:
ppublish
Résumé
Alzheimer's disease (AD) is a progressive, chronic and age-related neurodegenerative disorder that affects millions of people across the world. In pursuit of new anti-AD remedies, 2-[Hydroxy-(4-nitrophenyl)methyl]-cyclopentanone (NMC), a β hydroxyl ketone derivative was studied to explore its neuroprotective potentials against AD. The in-vitro AChE and BuChE enzymes inhibition were evaluated by Ellman protocol and antioxidant potentials of NMC by DPPH free radical scavenging assay. In-vivo behavioral studies were performed in the transgenic 5xFAD mice model of AD using shallow water maze (SWM), Paddling Y-Maze (PYM), elevated plus maze (EPM) and balance beam (BB) tests. Also, the ex-vivo cholinesterase inhibitory effects of NMC and histopathological analysis of amyloid-β plaques were determined in the frontal cortex and hippocampal regions of the mice brain. NMC exhibited significant in vitro anti-cholinesterase enzyme potentials with an IC
Identifiants
pubmed: 33211296
doi: 10.1007/s11033-020-05997-0
pii: 10.1007/s11033-020-05997-0
doi:
Substances chimiques
Antioxidants
0
Cholinesterase Inhibitors
0
Cyclopentanes
0
Ketones
0
Neuroprotective Agents
0
Acetylcholinesterase
EC 3.1.1.7
Butyrylcholinesterase
EC 3.1.1.8
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
9553-9566Subventions
Organisme : Higher Education Commision, Pakistan
ID : NRPU 6671/KP/NRPU/R&D/HEC/2016