Photoswitchable Pseudoirreversible Butyrylcholinesterase Inhibitors Allow Optical Control of Inhibition in Vitro and Enable Restoration of Cognition in an Alzheimer's Disease Mouse Model upon Irradiation

J Am Chem Soc. 2022 Feb 23;144(7):3279-3284. doi: 10.1021/jacs.1c13492. Epub 2022 Feb 9.

Abstract

To develop tools to investigate the biological functions of butyrylcholinesterase (BChE) and the mechanisms by which BChE affects Alzheimer's disease (AD), we synthesized several selective, nanomolar active, pseudoirreversible photoswitchable BChE inhibitors. The compounds were able to specifically influence different kinetic parameters of the inhibition process by light. For one compound, a 10-fold difference in the IC50-values (44.6 nM cis, 424 nM trans) in vitro was translated to an "all or nothing" response with complete recovery in a murine cognition-deficit AD model at dosages as low as 0.3 mg/kg.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / chemically induced
  • Alzheimer Disease / drug therapy*
  • Amyloid beta-Peptides
  • Animals
  • Azo Compounds / chemical synthesis
  • Azo Compounds / metabolism
  • Azo Compounds / radiation effects
  • Azo Compounds / therapeutic use
  • Butyrylcholinesterase / metabolism*
  • Carbamates / chemical synthesis
  • Carbamates / metabolism
  • Carbamates / radiation effects
  • Carbamates / therapeutic use
  • Cholinesterase Inhibitors / chemical synthesis
  • Cholinesterase Inhibitors / metabolism
  • Cholinesterase Inhibitors / radiation effects
  • Cholinesterase Inhibitors / therapeutic use*
  • Cognition / drug effects*
  • Kinetics
  • Mice
  • Molecular Docking Simulation
  • Neuroprotective Agents / chemical synthesis
  • Neuroprotective Agents / metabolism
  • Neuroprotective Agents / radiation effects
  • Neuroprotective Agents / therapeutic use*
  • Nootropic Agents / chemical synthesis
  • Nootropic Agents / metabolism
  • Nootropic Agents / radiation effects
  • Nootropic Agents / therapeutic use*
  • Peptide Fragments
  • Protein Binding
  • Stereoisomerism

Substances

  • Amyloid beta-Peptides
  • Azo Compounds
  • Carbamates
  • Cholinesterase Inhibitors
  • Neuroprotective Agents
  • Nootropic Agents
  • Peptide Fragments
  • amyloid beta-protein (25-35)
  • Butyrylcholinesterase