Abstract
In rat cerebellar slices, 500 microM (RS)-alpha-methyl-4-carboxyphenylglycine (MCPG) reversibly inhibited both dendritic and somatic increases in FLUO-3 fluorescence intensity induced by bath applications of 50-100 microM (+-)-1-aminocyclopentane-trans-1,3-dicarboxylic acid (t-ACPD). No effect of MCPG was observed on dendritically recorded excitatory postsynaptic potentials evoked by synaptic activation of either parallel or climbing fibres. Long-term depression of parallel fibre-Purkinje cell transmission, induced either by conjunctive activation of parallel and climbing fibres or by pairing parallel fibre stimulation with intradendritic injections of 8-BrcGMP, was not only prevented in the presence of MCPG but a robust long-term potentiation of responses consistently occurred. These data show that metabotropic glutamate receptor activation is necessary for the induction of LTD.
MeSH terms
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Aniline Compounds
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Animals
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Benzoates / pharmacology
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Biotransformation / drug effects
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Biotransformation / physiology
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Cerebellum / drug effects
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Cerebellum / physiology*
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Cyclic GMP / analogs & derivatives
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Cyclic GMP / pharmacology
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Cycloleucine / analogs & derivatives
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Cycloleucine / pharmacology
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Cyclopropanes
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Evoked Potentials / drug effects
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Evoked Potentials / physiology
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Fluorescent Dyes
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Glycine / analogs & derivatives
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Glycine / pharmacology
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In Vitro Techniques
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Nerve Fibers / drug effects
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Nerve Fibers / physiology
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Neuronal Plasticity / drug effects
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Neuronal Plasticity / physiology*
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Neurotoxins / pharmacology
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Purkinje Cells / drug effects
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Purkinje Cells / physiology
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Rats
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Receptors, Metabotropic Glutamate / antagonists & inhibitors
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Receptors, Metabotropic Glutamate / physiology*
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Synaptic Transmission / physiology
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Xanthenes
Substances
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Aniline Compounds
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Benzoates
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Cyclopropanes
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Fluorescent Dyes
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Neurotoxins
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Receptors, Metabotropic Glutamate
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Xanthenes
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Cycloleucine
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1-amino-1,3-dicarboxycyclopentane
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alpha-methyl-4-carboxyphenylglycine
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Fluo-3
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8-bromocyclic GMP
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Cyclic GMP
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Glycine