Inhibition of Aβ peptide aggregation by ruthenium(II) polypyridyl complexes through copper chelation.

J Inorg Biochem

School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Education Mega Centre, No. 280, Waihuandong Road, Guangzhou 510006, PR China. Electronic address:

Published: November 2021

AI Article Synopsis

  • Alzheimer's disease (AD) is a complicated condition, and new compounds show potential as treatments by targeting metal ions and amyloid beta peptides (Aβ).
  • Researchers developed four hybrid compounds that use chelators like 8-hydroxyquinoline and designed them to capture copper (Cu) from Aβ, leading to improved efficiency in removing Cu and preventing Aβ assembly.
  • These compounds also inhibit harmful reactive oxygen species (ROS), protect mitochondria, and enhance neuron cell survival, representing a novel approach that combines hydrophobic interactions with metal ion chelation for AD therapy.

Article Abstract

Alzheimer's disease (AD) is known as a complex multifactorial syndrome and both metal chelators and amyloid β peptide (Aβ) inhibitors show promise against AD. Herein, four small hybrid compounds have been designed and synthesized utilizing 8-hydroxyquinoline, pyridine or imidazole as chelators and benzimidazole as the recognition moiety for AD treatment. These conjugates can capture Cu from Aβ and become dimers upon Cu coordination and show high efficiency for both Cu elimination and Aβ assembly inhibition. Besides, these designed complexes can inhibit the production of Aβ-induced reactive oxygen species (ROS), protect mitochondria from damage, and improve the survival rate of neuron cells. Our work provides a new strategy to combine hydrophobic interaction and metal ion chelation to design amyloid inhibitors.

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Source
http://dx.doi.org/10.1016/j.jinorgbio.2021.111591DOI Listing

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