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Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation
Ampakines are allosteric modulators of AMPA receptors that facilitate hippocampal long-term potentiation (LTP) and learning, and have been considered for the treatment of cognition and memory deficits. Here, we show that the ampakine CX546 raises the amplitude and slows the decay time of excitatory...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236409/ https://www.ncbi.nlm.nih.gov/pubmed/25403454 http://dx.doi.org/10.1101/lm.035220.114 |
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author | van Beugen, Boeke J. Qiao, Xin Simmons, Dana H. De Zeeuw, Chris I. Hansel, Christian |
author_facet | van Beugen, Boeke J. Qiao, Xin Simmons, Dana H. De Zeeuw, Chris I. Hansel, Christian |
author_sort | van Beugen, Boeke J. |
collection | PubMed |
description | Ampakines are allosteric modulators of AMPA receptors that facilitate hippocampal long-term potentiation (LTP) and learning, and have been considered for the treatment of cognition and memory deficits. Here, we show that the ampakine CX546 raises the amplitude and slows the decay time of excitatory postsynaptic currents (EPSCs) at cerebellar parallel fiber (PF) to Purkinje cell synapses, thus resembling CX546 effects described at hippocampal synapses. Using the fluorescent calcium indicator dye Oregon Green BAPTA-2 and an ultra-high-speed CCD camera, we also monitored calcium transients in Purkinje cell dendrites. In the presence of CX546 in the bath, PF-evoked calcium transients were enhanced and prolonged, suggesting that CX546 not only enhances synaptic transmission, but also boosts dendritic calcium signaling at cerebellar synapses. In contrast to previous observations in the hippocampus, however, CX546 applied during cerebellar recordings facilitates long-term depression (LTD) rather than LTP at PF synapses. These findings show that ampakines selectively modify the LTP–LTD balance depending on the brain area and type of synapse, and may provide tools for the targeted regulation of synaptic memories. |
format | Online Article Text |
id | pubmed-4236409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42364092015-12-01 Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation van Beugen, Boeke J. Qiao, Xin Simmons, Dana H. De Zeeuw, Chris I. Hansel, Christian Learn Mem Research Ampakines are allosteric modulators of AMPA receptors that facilitate hippocampal long-term potentiation (LTP) and learning, and have been considered for the treatment of cognition and memory deficits. Here, we show that the ampakine CX546 raises the amplitude and slows the decay time of excitatory postsynaptic currents (EPSCs) at cerebellar parallel fiber (PF) to Purkinje cell synapses, thus resembling CX546 effects described at hippocampal synapses. Using the fluorescent calcium indicator dye Oregon Green BAPTA-2 and an ultra-high-speed CCD camera, we also monitored calcium transients in Purkinje cell dendrites. In the presence of CX546 in the bath, PF-evoked calcium transients were enhanced and prolonged, suggesting that CX546 not only enhances synaptic transmission, but also boosts dendritic calcium signaling at cerebellar synapses. In contrast to previous observations in the hippocampus, however, CX546 applied during cerebellar recordings facilitates long-term depression (LTD) rather than LTP at PF synapses. These findings show that ampakines selectively modify the LTP–LTD balance depending on the brain area and type of synapse, and may provide tools for the targeted regulation of synaptic memories. Cold Spring Harbor Laboratory Press 2014-12 /pmc/articles/PMC4236409/ /pubmed/25403454 http://dx.doi.org/10.1101/lm.035220.114 Text en © 2014 van Beugen et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research van Beugen, Boeke J. Qiao, Xin Simmons, Dana H. De Zeeuw, Chris I. Hansel, Christian Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation |
title | Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation |
title_full | Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation |
title_fullStr | Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation |
title_full_unstemmed | Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation |
title_short | Enhanced AMPA receptor function promotes cerebellar long-term depression rather than potentiation |
title_sort | enhanced ampa receptor function promotes cerebellar long-term depression rather than potentiation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236409/ https://www.ncbi.nlm.nih.gov/pubmed/25403454 http://dx.doi.org/10.1101/lm.035220.114 |
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