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The Role of N-Methyl-d-Aspartate (NMDA) Receptors in Pain: A Review

Anesthesia & Analgesia · 2003 · Vol. 97(4) · pp. 1108–1116
Andrei B. PetrenkoTomohiro YamakuraHiroshi BabaKoki Shimoji

Abstract

There is accumulating evidence to implicate the importance of N-methyl-D-aspartate (NMDA) receptors to the induction and maintenance of central sensitization during pain states. However, NMDA receptors may also mediate peripheral sensitization and visceral pain. NMDA receptors are composed of NR1, NR2 (A, B, C, and D), and NR3 (A and B) subunits, which determine the functional properties of native NMDA receptors. Among NMDA receptor subtypes, the NR2B subunit-containing receptors appear particularly important for nociception, thus leading to the possibility that NR2B-selective antagonists may be useful in the treatment of chronic pain.

Pain Mechanisms and TreatmentsNeuroscience and Neuropharmacology ResearchIon channel regulation and functionNMDA receptorReceptorNociceptionSensitizationNeuroscienceGlutamate receptorLong-term depressionPharmacologyChemistryMedicine

MeSH terms

AnimalsCentral Nervous SystemChronic DiseaseHumansPainReceptors, N-Methyl-D-AspartatePeripheral Nervous SystemExcitatory Amino Acid Agonists
Citations
660
FWCI
11.27
field-weighted impact
References
82
Percentile
99%
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