The use of mouse models to understand and improve cognitive deficits in Down syndrome

Dis Model Mech. 2011 Sep;4(5):596-606. doi: 10.1242/dmm.007716. Epub 2011 Aug 4.

Abstract

Remarkable advances have been made in recent years towards therapeutics for cognitive impairment in individuals with Down syndrome (DS) by using mouse models. In this review, we briefly describe the phenotypes of mouse models that represent outcome targets for drug testing, the behavioral tests used to assess impairments in cognition and the known mechanisms of action of several drugs that are being used in preclinical studies or are likely to be tested in clinical trials. Overlaps in the distribution of targets and in the pathways that are affected by these diverse drugs in the trisomic brain suggest new avenues for DS research and drug development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Behavior, Animal
  • Brain / pathology
  • Brain / physiopathology
  • Clinical Trials as Topic
  • Cognition Disorders / complications*
  • Cognition Disorders / physiopathology
  • Disease Models, Animal*
  • Down Syndrome / complications*
  • Down Syndrome / drug therapy
  • Down Syndrome / physiopathology
  • Humans
  • Mice