Induction of autophagy by a novel small molecule improves aβ pathology and ameliorates cognitive deficits

PLoS One. 2013 Jun 4;8(6):e65367. doi: 10.1371/journal.pone.0065367. Print 2013.

Abstract

Growing evidence has demonstrated a neuroprotective role of autophagy in Alzheimer's disease (AD). Thus, autophagy has been regarded as a potential therapeutic target, attracting increasing interest in pharmaceutical autophagy modulation by small molecules. We designed a two-cycle screening strategy on the basis of imaging high-throughout screening (HTS) and cellular toxicity assay, and have identified a novel autophagy inducer known as GTM-1. We further showed that GTM-1 exhibits dual activities, such as autophagy induction and antagonism against Aβ-oligomer toxicity. GTM-1 modulates autophagy in an Akt-independent and mTOR-independent manner. In addition, we demonstrated that GTM-1 enhances autophagy clearance and reverses the downregulation of autophagy flux by thapsigargin and asparagine. Furthermore, administration of GTM-1 attenuated Aβ pathology and ameliorated cognitive deficits in AD mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology
  • Amyloid beta-Peptides / chemistry*
  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Autophagy / drug effects*
  • Cell Line, Tumor
  • Cognition / drug effects*
  • Drug Evaluation, Preclinical
  • High-Throughput Screening Assays
  • Humans
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Memory / drug effects
  • Mice
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / pathology
  • Neuroprotective Agents / adverse effects
  • Neuroprotective Agents / pharmacology*
  • Neuroprotective Agents / therapeutic use
  • Oxidative Stress / drug effects
  • Peptide Fragments / chemistry*
  • Peptide Fragments / toxicity*
  • Protein Multimerization / drug effects
  • Protein Structure, Secondary
  • Quinazolines / adverse effects
  • Quinazolines / pharmacology*
  • Quinazolines / therapeutic use
  • Small Molecule Libraries / adverse effects
  • Small Molecule Libraries / pharmacology*
  • Small Molecule Libraries / therapeutic use

Substances

  • Amyloid beta-Peptides
  • GTM-1 compound
  • Neuroprotective Agents
  • Peptide Fragments
  • Quinazolines
  • Small Molecule Libraries
  • amyloid beta-protein (1-42)