Abstract
Several synaptic depression mechanisms have been described for the hippocampus, cerebellum and neocortex in vitro, but little is known about which, if any, are engaged during experience-dependent depression (EDD). We found that EDD in the mouse barrel cortex depends on the AMPA subunit GluR1 in layers II/III and IV, but not in layer V, and that long-term depression is also GluR1 dependent in the IV-II/III, but not II/III-V, pathway.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Analysis of Variance
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Animals
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Long-Term Synaptic Depression / genetics
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Long-Term Synaptic Depression / physiology*
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Mice
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Mice, Knockout
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Receptors, AMPA / deficiency
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Receptors, AMPA / physiology*
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Sensory Deprivation / physiology
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Somatosensory Cortex / anatomy & histology*
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Somatosensory Cortex / physiology*
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Synaptic Transmission / genetics
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Synaptic Transmission / physiology*
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Vibrissae / innervation
Substances
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Receptors, AMPA
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glutamate receptor ionotropic, AMPA 1