Abstract
The necessity of metabotropic glutamate receptors (mGluRs) in the induction of long-term potentiation (LTP) has recently been questioned. We examined the effect of (R,S)-alpha-methyl-4-caboxyphenylglycine (MCPG), a selective mGluR antagonist, on two independent forms of LTP. One form induced by a 25 Hz/1 s tetanus is solely N-methyl-D-aspartate (NMDA) receptor-dependent. The other form induced by four 200 Hz/0.5 s bursts in the presence of APV is NMDA receptor-independent. In both paradigms the presence of MCPG prevented the induction of LTP by afferent activation.
MeSH terms
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Animals
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Benzoates / pharmacology*
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Calcium Channels / drug effects
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Calcium Channels / metabolism
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Calcium Channels / physiology
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Electric Stimulation
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Electrophysiology
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Excitatory Amino Acid Antagonists / pharmacology*
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Glycine / analogs & derivatives*
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Glycine / pharmacology
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Hippocampus / drug effects
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Hippocampus / physiology*
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In Vitro Techniques
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Ion Channel Gating / drug effects
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Long-Term Potentiation / drug effects*
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Rats
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Receptors, Metabotropic Glutamate / antagonists & inhibitors*
Substances
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Benzoates
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Calcium Channels
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Excitatory Amino Acid Antagonists
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Receptors, Metabotropic Glutamate
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alpha-methyl-4-carboxyphenylglycine
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Glycine