Abstract
In the Xenopus oocyte preparation, D-cycloserine (DCS) had the profile of a partial agonist at the glycine modulatory site of the NMDA receptor. Maximal NMDA responses in the presence of DCS were only 40-50% of those in the presence of glycine. Glycine and D-serine were agonists at this site. The actions of DCS were competitively antagonized by HA-966, a known glycine antagonist.
MeSH terms
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Animals
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Cycloserine / pharmacology*
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Glycine / pharmacology
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Glycine / physiology*
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Oocytes / metabolism
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Oocytes / physiology*
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Pyrrolidinones / pharmacology
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RNA, Messenger
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Rats
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Receptors, N-Methyl-D-Aspartate
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Receptors, Neurotransmitter / drug effects*
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Receptors, Neurotransmitter / physiology
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Xenopus laevis
Substances
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Pyrrolidinones
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RNA, Messenger
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Receptors, N-Methyl-D-Aspartate
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Receptors, Neurotransmitter
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Cycloserine
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1-hydroxy-3-amino-2-pyrrolidone
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Glycine