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Fucoxanthin Inhibits β-Amyloid Assembly and Attenuates β-Amyloid Oligomer-Induced Cognitive Impairments.

Abstract
β-Amyloid (Aβ) can form aggregates through self-assembly and produce neurotoxicity in the early stage of Alzheimer's disease (AD). Therefore, the inhibition of Aβ assembly is considered as the primary target for AD therapy. In this study, we reported that fucoxanthin, a marine carotenoid, potently reduced the formation of Aβ fibrils and oligomers. Moreover, the fucoxanthin-triggered modification significantly reduced the neurotoxicity of Aβ oligomers in vitro. Molecular dynamics simulation analysis further revealed a hydrophobic interaction between fucoxanthin and Aβ peptide, which might prevent the conformational transition and self-assembly of Aβ. Most importantly, fucoxanthin could attenuate cognitive impairments in Aβ oligomer-injected mice. In addition, fucoxanthin significantly inhibited oxidative stress, enhanced the expression of brain-derived neurotrophic factor, and increased ChAT-positive regions in the hippocampus of mice. On the basis of these novel findings, we anticipated that fucoxanthin might ameliorate AD via inhibiting Aβ assembly and attenuating Aβ neurotoxicity.
AuthorsSiying Xiang, Fufeng Liu, Jiajia Lin, Huixin Chen, Chunhui Huang, Liping Chen, Yiying Zhou, Luying Ye, Ke Zhang, Jiukai Jin, Jiacheng Zhen, Chuang Wang, Shan He, Qinwen Wang, Wei Cui, Jinrong Zhang
JournalJournal of agricultural and food chemistry (J Agric Food Chem) Vol. 65 Issue 20 Pg. 4092-4102 (May 24 2017) ISSN: 1520-5118 [Electronic] United States
PMID28478680 (Publication Type: Journal Article)
Chemical References
  • Amyloid beta-Peptides
  • Brain-Derived Neurotrophic Factor
  • Xanthophylls
  • fucoxanthin
Topics
  • Alzheimer Disease (drug therapy, genetics, metabolism, psychology)
  • Amyloid beta-Peptides (chemistry, metabolism)
  • Animals
  • Brain-Derived Neurotrophic Factor (genetics, metabolism)
  • Cell Survival (drug effects)
  • Cognition (drug effects)
  • Hippocampus (drug effects, metabolism)
  • Humans
  • Male
  • Mice
  • Mice, Inbred ICR
  • Molecular Docking Simulation
  • Neurons (drug effects, metabolism)
  • Xanthophylls (administration & dosage)

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