NMDA agonists and antagonists as probes of glutamatergic dysfunction and pharmacotherapies in neuropsychiatric disorders

Harv Rev Psychiatry. 1999 Sep-Oct;7(3):125-43.

Abstract

Antagonists of the N-methyl-D-aspartate (NMDA) subclass of glutamate receptors and agonists of the glycine-B coagonist site of these receptors have been important tools for characterizing the contributions of NMDA receptor pathophysiology to a large number of neuropsychiatric conditions and for treating these conditions. Among these disorders are Alzheimer's disease, chronic pain syndromes, epilepsy, schizophrenia, Parkinson's disease, Huntington's disease, addiction disorders, major depression, and anxiety disorders. This review will examine pathophysiological and therapeutic hypotheses generated or supported by clinical studies employing NMDA antagonists and glycine-B agonists and partial agonists. It will also consider ethical issues related to human psychopharmacological studies employing glutamatergic probes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Brain Diseases / drug therapy*
  • Brain Diseases / metabolism
  • Chronic Disease
  • Ethics, Medical
  • Human Experimentation
  • Humans
  • Mental Disorders / drug therapy*
  • Mental Disorders / metabolism
  • Pain / drug therapy*
  • Pain / metabolism
  • Receptors, Glycine / agonists*
  • Receptors, Glycine / metabolism
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Syndrome
  • United States

Substances

  • Receptors, Glycine
  • Receptors, N-Methyl-D-Aspartate