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Vol. 300, Issue 3, 717-723, March 2002
Departments of Neurology (D.R.L.), Pediatrics (D.R.L.), and
Pharmacology (R.P.G.), University of Pennsylvania and The Children's
Hospital of Philadelphia, Philadelphia, Pennsylvania
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. The
N-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.
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