Excitotoxicity: Perspectives Based on N-Methyl-d-Aspartate Receptor Subtypes
- 1 March 2002
- journal article
- review article
- Published by Elsevier in The Journal of Pharmacology and Experimental Therapeutics
- Vol. 300 (3) , 717-723
- https://doi.org/10.1124/jpet.300.3.717
Abstract
Since excitotoxicity has been implicated in a variety of neuropathological conditions, understanding the pathways involved in this type of cell death is of critical importance to the future clinical treatment of many diseases. TheN-methyl-d-aspartate (NMDA) receptor has become a primary focus of excitotoxic research because early studies demonstrated that antagonism of this receptor subtype was neuroprotective. However, initial pharmacological agents were not clinically useful due to the adverse effects of complete NMDA receptor blockade. Understanding the biochemical properties of the multitude of NMDA receptor subtypes offers the possibility of developing more effective and clinically useful drugs. With the discovery of the basis of heterogeneity of NMDA receptors through molecular biological approaches, many new potential therapeutic targets have been uncovered, and several model systems have been developed for the study of NMDA receptor-mediated cell death. This review discusses these models and the current understanding of the relationship between NMDA receptor subtypes and excitotoxicity.Keywords
This publication has 49 references indexed in Scilit:
- Calcium buffering and protection from excitotoxic cell death by exogenous calbindin-D28k in HEK 293 cellsCell Calcium, 2001
- Mutant Huntingtin Enhances Excitotoxic Cell DeathMolecular and Cellular Neuroscience, 2001
- Antiparkinsonian Actions of CP-101,606, an Antagonist of NR2B Subunit-Containing N-Methyl--Aspartate ReceptorsExperimental Neurology, 2000
- Effects of Depolarization and NMDA Antagonists on the Survival of Cerebellar Granule Cells: A Pivotal Role for Protein Kinase C IsoformsJournal of Neurochemistry, 1997
- N-Methyl-D-aspartate Receptors Expressed in a Nonneuronal Cell Line Mediate Subunit-specific Increases in Free Intracellular CalciumJournal of Biological Chemistry, 1997
- Glutamate Receptor Ion Channel Properties Predict Vulnerability to Cytotoxicity in a Transfected Nonneuronal Cell LineMolecular and Cellular Neuroscience, 1996
- Delayed Antagonism of Calpain Reduces Excitotoxicity in Cultured NeuronsStroke, 1995
- Secondary mechanisms in neuronal traumaCurrent Opinion in Neurology, 1994
- Interleukin-1β inhibits Ca2+ channel currents in hippocampal neurons through protein kinase CEuropean Journal of Pharmacology: Molecular Pharmacology, 1994
- Developmental switch in the expression of NMDA receptors occurs in vivo and in vitroNeuron, 1993