Multifunctional, Fluorene-Based Modulator of Cholinergic and GABAergic Neurotransmission as a Novel Drug Candidate for Palliative Treatment of Alzheimer's Disease

Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202420510. doi: 10.1002/anie.202420510. Epub 2024 Nov 22.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by memory loss and behavioral and psychological symptoms of dementia (BPSD). Given that cholinergic neurons are predominantly affected in AD, current treatments primarily aim to enhance cholinergic neurotransmission. However, imbalances in other neurotransmitters, such as γ-aminobutyric acid (GABA), also contribute to AD symptomatology. In the presented research, using a combination of crystallography and computational methods we developed compound 6 as a dual modulator of GABAergic and cholinergic neurotransmission systems. Compound 6 demonstrated inhibition of BuChE (IC50=0.21 μM) and GABA transporter 1 (IC50=10.96 μM) and 3 (IC50=7.76 μM), along with a favorable drug-likeness profile. Subsequent in vivo studies revealed the effectiveness of 6 in enhancing memory retention and alleviating anxiety and depression symptoms in animal models, while also proving safe and bioavailable for oral administration. The innovative multi-target-directed ligand 6 offers a new approach to treating cognitive deficits and BPSD in AD.

Keywords: Alzheimer's disease; GABA transporters; butyrylcholinesterase; inhibitors; multitarget drugs.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Alzheimer Disease* / drug therapy
  • Alzheimer Disease* / metabolism
  • Animals
  • Butyrylcholinesterase / metabolism
  • Cholinesterase Inhibitors* / chemistry
  • Cholinesterase Inhibitors* / pharmacology
  • Cholinesterase Inhibitors* / therapeutic use
  • Fluorenes* / chemistry
  • Fluorenes* / pharmacology
  • Fluorenes* / therapeutic use
  • GABA Plasma Membrane Transport Proteins / metabolism
  • Humans
  • Mice
  • Molecular Structure
  • Synaptic Transmission* / drug effects
  • gamma-Aminobutyric Acid* / metabolism

Substances

  • Fluorenes
  • Cholinesterase Inhibitors
  • GABA Plasma Membrane Transport Proteins
  • Butyrylcholinesterase
  • gamma-Aminobutyric Acid
  • Acetylcholinesterase