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Mulberry Diels-Alder-type adducts from Morus alba as multi-targeted agents for Alzheimer's disease.
- Source :
-
Phytochemistry [Phytochemistry] 2019 Jan; Vol. 157, pp. 82-91. Date of Electronic Publication: 2018 Nov 01. - Publication Year :
- 2019
-
Abstract
- Mulberry Diels-Alder-type adducts (MDAAs) are a group of structurally unique natural products biosynthetically derived from the intermolecular [4 + 2] cycloaddition of a dehydroprenylphenol and a chalcone. In the current study, ten MDAAs, including an undescribed one, inethermulberrofuran C, were isolated from the root bark of Morus alba. The anti-Alzheimer's disease (anti-AD) properties of these isolates were systematically screened for a series of potential targets (Aβ self-aggregation, tau aggregation, and ChEs) as well as the anti-neuroinflammatory and neuroprotective activities. Four compounds, mulberrofuran C, mulberrofuran K, mulberrofuran G, and isomulberrofuran G, turned out to be potent multi-targeted agents for AD. Among them, mulberrofuran K with a good blood-brain barrier (BBB) permeability (8.7 ± 0.3 × 10 <superscript>-6</superscript> cm/s) was selected as a promising candidate for further mechanism study in glutamate-induced HT22 cell model, which showed its neuroprotective ability on up-regulation of the glutathione (GSH) level and suppression of the reactive oxygen species (ROS) production.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Subjects :
- Amyloid beta-Peptides chemistry
Biological Products metabolism
Biological Products therapeutic use
Blood-Brain Barrier metabolism
Cell Line
Cholinesterase Inhibitors metabolism
Cholinesterase Inhibitors pharmacology
Cholinesterase Inhibitors therapeutic use
Dose-Response Relationship, Drug
Glutathione metabolism
Humans
Peptide Fragments chemistry
Permeability
Protein Aggregates drug effects
Reactive Oxygen Species metabolism
Up-Regulation drug effects
Alzheimer Disease drug therapy
Biological Products pharmacology
Morus chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3700
- Volume :
- 157
- Database :
- MEDLINE
- Journal :
- Phytochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 30390605
- Full Text :
- https://doi.org/10.1016/j.phytochem.2018.10.028