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ModuEation of the NMDA receptor by D-serine in the cortex and the spinal cord, in vitro

Authors
Journal
European Journal of Pharmacology
0014-2999
Publisher
Elsevier
Publication Date
Volume
191
Issue
1
Identifiers
DOI: 10.1016/0014-2999(90)94093-d
Keywords
  • Nmda (N-Methyl-D-Aspartate)
  • 7-Chlorokynurenic Acid
  • Ha-966
  • Glycine
  • Spinal Cord
  • Cortical Wedge
  • (Electrophysiology)

Abstract

Abstract We present a comparative study of the modulation of the N-methyl-D-aspartate (NMDA) receptor at the strychnine-insensitive glycine site in the spinal cord and in the cortex. The excitatory effect of NMDA was potentiated by D-serine (a glycine mimetic) in the hemisected rat spinal cord. The non-competitive NMDA antagonists 7-chlorokynurenic acid (7-C1 KYNA; 10 μM) and 3-aimno-l-hydroxypyrrolid-2-one (HA-966; 100 or 200 μM) antagonized the effect of NMDA in the spinal cord and cortical wedge preparation. The antagonism was reversed by the addition of D-serine. This effect was strychnine-insensitive and hence not related to the inhibitory glycine receptor known to be present in the spinal cord. Our results suggest strongly that glycine positively modulates the NMDA system not only at a supraspinal level but also at the spinal level. As the positive modulation of NMDA responses by D-serine was also seen in the presence of tetrodotoxin, we conclude that the NMDA/glycine complex is (also) located on motoneurones in addition to the known glycine-mediated inhibitory system.

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