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Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons
Although contextual learning requires plasticity at both excitatory and inhibitory (E/I) synapses in cornu ammonis 1 (CA1) neurons, the temporal dynamics across the neuronal population are poorly understood. Using an inhibitory avoidance task, we analyzed the dynamic changes in learning-induced E/I...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Federation of American Societies for Experimental Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894079/ https://www.ncbi.nlm.nih.gov/pubmed/31689120 http://dx.doi.org/10.1096/fj.201801893RRR |
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author | Sakimoto, Yuya Kida, Hiroyuki Mitsushima, Dai |
author_facet | Sakimoto, Yuya Kida, Hiroyuki Mitsushima, Dai |
author_sort | Sakimoto, Yuya |
collection | PubMed |
description | Although contextual learning requires plasticity at both excitatory and inhibitory (E/I) synapses in cornu ammonis 1 (CA1) neurons, the temporal dynamics across the neuronal population are poorly understood. Using an inhibitory avoidance task, we analyzed the dynamic changes in learning-induced E/I synaptic plasticity. The training strengthened GABA(A) receptor–mediated synapses within 1 min, peaked at 10 min, and lasted for over 60 min. The intracellular loop (Ser(408−409)) of GABA(A) receptor β(3) subunit was also phosphorylated within 1 min of training. As the results of strengthening of α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate receptor–mediated synapses, CA1 pyramidal neurons exhibited broad diversity of E/I synaptic currents within 5 min. Moreover, presynaptic glutamate release probability at basal dendrites also increased within 5 min. To further quantify the diversified E/I synaptic currents, we calculated self-entropy (bit) for individual neurons. The neurons showed individual levels of the parameter, which rapidly increased within 1 min of training and maintained for over 60 min. These results suggest that learning-induced synaptic plasticity is critical immediately following encoding rather than during the retrieval phase of the learning. Understanding the temporal dynamics along with the quantification of synaptic diversity would be necessary to identify a failure point for learning-promoted plasticity in cognitive disorders.—Sakimoto, Y., Kida, H., Mitsushima, D. Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons. |
format | Online Article Text |
id | pubmed-6894079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Federation of American Societies for Experimental Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-68940792019-12-10 Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons Sakimoto, Yuya Kida, Hiroyuki Mitsushima, Dai FASEB J Research Although contextual learning requires plasticity at both excitatory and inhibitory (E/I) synapses in cornu ammonis 1 (CA1) neurons, the temporal dynamics across the neuronal population are poorly understood. Using an inhibitory avoidance task, we analyzed the dynamic changes in learning-induced E/I synaptic plasticity. The training strengthened GABA(A) receptor–mediated synapses within 1 min, peaked at 10 min, and lasted for over 60 min. The intracellular loop (Ser(408−409)) of GABA(A) receptor β(3) subunit was also phosphorylated within 1 min of training. As the results of strengthening of α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate receptor–mediated synapses, CA1 pyramidal neurons exhibited broad diversity of E/I synaptic currents within 5 min. Moreover, presynaptic glutamate release probability at basal dendrites also increased within 5 min. To further quantify the diversified E/I synaptic currents, we calculated self-entropy (bit) for individual neurons. The neurons showed individual levels of the parameter, which rapidly increased within 1 min of training and maintained for over 60 min. These results suggest that learning-induced synaptic plasticity is critical immediately following encoding rather than during the retrieval phase of the learning. Understanding the temporal dynamics along with the quantification of synaptic diversity would be necessary to identify a failure point for learning-promoted plasticity in cognitive disorders.—Sakimoto, Y., Kida, H., Mitsushima, D. Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons. Federation of American Societies for Experimental Biology 2019-12 2019-11-05 /pmc/articles/PMC6894079/ /pubmed/31689120 http://dx.doi.org/10.1096/fj.201801893RRR Text en © The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Sakimoto, Yuya Kida, Hiroyuki Mitsushima, Dai Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons |
title | Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons |
title_full | Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons |
title_fullStr | Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons |
title_full_unstemmed | Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons |
title_short | Temporal dynamics of learning-promoted synaptic diversity in CA1 pyramidal neurons |
title_sort | temporal dynamics of learning-promoted synaptic diversity in ca1 pyramidal neurons |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894079/ https://www.ncbi.nlm.nih.gov/pubmed/31689120 http://dx.doi.org/10.1096/fj.201801893RRR |
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