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NMDA receptor antagonists as analgesics: focus on the NR2B subtype
Authors:Boris A. Chizh   P. Max Headley  Thomas M. Tzschentke
Affiliation:

a Dept of Pharmacology, Grünenthal GmbH Research & Development, Zieglerstr. 6, 52078 Aachen, Germany

b Dept of Physiology, University of Bristol, Bristol, UK BS8 1TD.

c Dept of Pharmacology, Grünenthal GmbH Research & Development, Zieglerstr. 6, 52078 Aachen, Germany

Abstract:Ifenprodil and a group of related compounds are selective antagonists of NR2B-containing NMDA receptors. These compounds are antinociceptive in a variety of preclinical pain models and have a much lower side-effect profile compared with other NMDA receptor antagonists. It remains unclear whether the improved safety of these compounds is due to their subtype selectivity or to a unique mode of inhibition of the receptor. Human trials have so far confirmed the good tolerability of these subtype-selective NMDA receptor antagonists; however, whether they are as effective as other NMDA receptor antagonists in pain patients remains to be demonstrated.
Keywords:nociception   NMDA receptors   NR2B subunit   side-effects   neurotoxicity   dependence   psychotomimetic action
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