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)

Grants and funding

This study was supported by the First People’s Hospital of Yangzhou and Changzheng Hospital. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.