Repurposing GLP1 agonists for neurodegenerative diseases

Int Rev Neurobiol. 2020:155:91-112. doi: 10.1016/bs.irn.2020.02.007. Epub 2020 Aug 11.

Abstract

There is a large unmet medical need to find disease modifying therapies against neurodegenerative diseases. This review summarizes data indicating that insulin resistance occurs in neurodegeneration and strategies to normalize insulin sensitivity in neurons may provide neuroprotective actions. In particular, recent preclinical and clinical studies in Parkinson's disease and Alzheimer's disease have indicated that glucagon-like peptide 1 (GLP1) agonism and dipeptidyl peptidase-4 inhibition may exert neuroprotection. Mechanistic insights from these studies and future directions for drug development against neurodegeneration based on GLP1 agonism are discussed.

Keywords: Alzheimer's disease; GLP1; Insulin; Neurodegenerative diseases; Parkinson's disease.

Publication types

  • Review

MeSH terms

  • Animals
  • Cognition Disorders / drug therapy
  • Cognition Disorders / etiology
  • Dipeptidyl-Peptidase IV Inhibitors / therapeutic use
  • Drug Repositioning*
  • Glucagon-Like Peptide 1 / agonists*
  • Humans
  • Hypoglycemic Agents / therapeutic use*
  • Insulin / physiology
  • Neurodegenerative Diseases / drug therapy*
  • Neurodegenerative Diseases / psychology
  • Neuroprotective Agents / therapeutic use*

Substances

  • Dipeptidyl-Peptidase IV Inhibitors
  • Hypoglycemic Agents
  • Insulin
  • Neuroprotective Agents
  • Glucagon-Like Peptide 1