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Journal ArticleDOI

Synaptic activation of AMPA receptors inhibits GABA release from cerebellar interneurons.

TLDR
Dual AMPA receptor-mediated functions of excitation and disinhibition may ensure transmission of cerebellar CF signals controlling sensorimotor coordination.
Abstract
A single neurotransmitter elicits diverse physiological responses through activation of multiple receptor subtypes and/or heterosynaptic interactions involving distinct synaptic targets. We found that a typical excitatory transmitter released from the climbing fiber (CF) in the cerebellar cortex not only excited Purkinje cells directly but also presynaptically inhibited GABAergic transmission from interneurons converging on the same Purkinje cells. Both homosynaptic and heterosynaptic actions of the CF transmitter (possibly glutamate) were mediated by activation of AMPA receptors. Dual AMPA receptor-mediated functions of excitation and disinhibition may ensure transmission of cerebellar CF signals controlling sensorimotor coordination.

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Citations
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Journal ArticleDOI

AMPA Receptor Trafficking at Excitatory Synapses

TL;DR: This work has shown that neuronal activity controls synaptic AMPA receptor trafficking, and this dynamic process plays a key role in the synaptic plasticity that is thought to underlie aspects of learning and memory.
Journal ArticleDOI

Cerebellar Long-Term Depression: Characterization, Signal Transduction, and Functional Roles

Masao Ito
TL;DR: Roles of LTD are defined in the light of the microcomplex concept of the cerebellum as functionally eliminating those synaptic connections associated with errors during repeated exercises, while preserving other connections leading to the successful execution of movements.
Journal ArticleDOI

ATP Released by Astrocytes Mediates Glutamatergic Activity-Dependent Heterosynaptic Suppression

TL;DR: It is reported that ATP released from astrocytes as a result of neuronal activity can also modulate central synaptic transmission, and neuron-glia crosstalk may participate in activity-dependent synaptic modulation.
Journal ArticleDOI

Presynaptic ionotropic receptors and control of transmitter release

TL;DR: This review considers the criteria that should be met to identify a presynaptic ionotropic receptor and its regulatory function and review several examples ofpresynaptic receptors that meet at least some of those criteria.
Journal ArticleDOI

Distributed synergistic plasticity and cerebellar learning

TL;DR: It is proposed that the different forms of plasticity in the granular layer and the molecular layer operate synergistically in a temporally and spatially distributed manner, so as to ultimately create optimal output for behaviour.
References
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Journal Article

The glutamate receptor ion channels

TL;DR: The cloning of cDNAs encoding glutamate receptor subunits, which occurred mainly between 1989 and 1992, stimulated the development of ionotropic glutamate receptors in the brain.
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Pharmacology and functions of metabotropic glutamate receptors.

TL;DR: The findings suggest that the mGluRs provide a novel target for development of therepeutic agents that could have a significant impact on neuropharmacology.
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A family of AMPA-selective glutamate receptors

TL;DR: Four cloned cDNAs encoding 900-amino acid putative glutamate receptors with approximately 70 percent sequence identity were isolated from a rat brain cDNA library and in situ hybridization revealed differential expression patterns of the cognate mRNAs throughout the brain.
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Long-term depression

TL;DR: Evidence is accumulating to support the cerebellar learning hypothesis as to how long the LTD lasts beyond the limit of the present maximum observation time of 3 hr, and whether and how it is eventually transformed to a permanent memory.
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Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain.

TL;DR: Staining was most prominent in forebrain structures such as the olfactory bulb and tubercle, septal nuclei, amygdaloid complex, hippocampus, induseum griseum, habenula, and interpeduncular nucleus, and in the cerebellum, with limited evidence of stained presynaptic terminals, excepting Bergmann glia.
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