MODULATION OF THE NMDA RECEPTOR BY D-SERINE IN THE CORTEX AND THE SPINAL-CORD, INVITRO

被引:27
作者
BRUGGER, F
WICKI, U
NASSENSTEINELTON, D
FAGG, GE
OLPE, HR
POZZA, MF
机构
[1] Research and Development Department, Pharmaceuticals Division, Ciba-Geigy, Ltd.
关键词
(Electrophysiology); 7-Chlorokynurenic acid; Cortical wedge; Glycine; HA-966; NMDA (N-methyl-D-aspartate); Spinal cord;
D O I
10.1016/0014-2999(90)94093-D
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. © 1990.
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页码:29 / 38
页数:10
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