Journal
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 166, Issue -, Pages 11-21Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2019.01.039
Keywords
Chalcone derivatives; Amyloid-beta aggregation inhibition; Ferroptosis inhibition; Alzheimer's disease
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Funding
- Fund of Innovation Center of Radiation Application, China [KFZC2018040208]
- National Key Scientific Instrument and Equipment Project of the Ministry of Science and Technology of China [2013YQ03059514]
- Beijing Institute of Technology Research Fund Program for Young Scholars
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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-beta peptide (A beta) aggregation as well as ferroptosis simultaneously. Thiofiavin-T assay indicated trihydroxy chalcones inhibited A beta aggregation better. In human neuroblastoma SH-SY5Y cells, cytoprotective chalcones 14a-c with three hydroxyl substituents exhibited a significant neuroprotection against A beta(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 A beta(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 A beta(1-42) aggregation and ferroptosis. (C) 2019 Elsevier Masson SAS. All rights reserved.
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