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On the role of synthesized hydroxylated chalcones as dual functional amyloid-β aggregation and ferroptosis inhibitors for potential treatment of Alzheimer's disease.
- Source :
-
European Journal of Medicinal Chemistry . Mar2019, Vol. 166, p11-21. 11p. - Publication Year :
- 2019
-
Abstract
- Abstract In addition to amyloid cascade hypothesis, ferroptosis – a recently identified cell death pathway associated with the accumulation of lipid hydroperoxides – was hypothesized as one of the main forms of cell death in Alzheimer's disease. Herein, a series of hydroxylated chalcones were designed and synthesized as dual-functional inhibitors to inhibit amyloid-β peptide (Aβ) aggregation as well as ferroptosis simultaneously. Thioflavin-T assay indicated trihydroxy chalcones inhibited Aβ aggregation better. In human neuroblastoma SH-SY5Y cells, cytoprotective chalcones 14a-c with three hydroxyl substituents exhibited a significant neuroprotection against Aβ 1-42 aggregation induced toxicity. In addition, chalcones 14a-c were found to be good inhibitors of ferroptosis induced by either pharmacological inhibition of the hydroperoxide-detoxifying enzyme Gpx4 using (1S, 3R)-RSL4 or cystine/glutamate antiporter system X c − inhibition by erastin through lipid peroxidation inhibition mechanism. Trihydroxy chalcone 14a was also able to completely subvert lipid peroxidation induced by Aβ 1-42 aggregation in SH-SY5Y cells indicating that they can reduce the neurotoxicity involved with oxidative stress. Compound 14a-c showed good ADMET properties and blood-brain barrier penetration in silico simulation software. From these data, a picture emerges wherein trihydroxy chalcones are potential candidates for the treatment of Alzheimer's disease by simultaneously inhibition of Aβ 1-42 aggregation and ferroptosis. Graphical abstract Image 1 Highlights • Hydroxylated chalcones were synthesized as dual-functional inhibitors. • Chalcones 14a-c inhibited amyloid-β aggregation at micromolar concentrations. • Chalcones 14a-c protected neural cells against Aβ aggregation induced toxicity. • Chalcones 14a-c protected cells from ferroptosis at micromolar concentrations. [ABSTRACT FROM AUTHOR]
- Subjects :
- *HYDROXYLATION
*HYDROPEROXIDES
*ALZHEIMER'S disease
*CHALCONES
*LIPIDS
Subjects
Details
- Language :
- English
- ISSN :
- 02235234
- Volume :
- 166
- Database :
- Academic Search Index
- Journal :
- European Journal of Medicinal Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 134864311
- Full Text :
- https://doi.org/10.1016/j.ejmech.2019.01.039