Cargando…
A critical period for learning and plastic changes at hippocampal CA1 synapses
Postnatal development of hippocampal function has been reported in many mammalian species, including humans. To obtain synaptic evidence, we analyzed developmental changes in plasticity after an inhibitory avoidance task in rats. Learning performance was low in infants (postnatal 2 weeks) but clearl...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065057/ https://www.ncbi.nlm.nih.gov/pubmed/35504922 http://dx.doi.org/10.1038/s41598-022-10453-z |
_version_ | 1784699501220462592 |
---|---|
author | Sakimoto, Yuya Shintani, Ako Yoshiura, Daiki Goshima, Makoto Kida, Hiroyuki Mitsushima, Dai |
author_facet | Sakimoto, Yuya Shintani, Ako Yoshiura, Daiki Goshima, Makoto Kida, Hiroyuki Mitsushima, Dai |
author_sort | Sakimoto, Yuya |
collection | PubMed |
description | Postnatal development of hippocampal function has been reported in many mammalian species, including humans. To obtain synaptic evidence, we analyzed developmental changes in plasticity after an inhibitory avoidance task in rats. Learning performance was low in infants (postnatal 2 weeks) but clearly improved from the juvenile period (3–4 weeks) to adulthood (8 weeks). One hour after the training, we prepared brain slices and sequentially recorded miniature excitatory postsynaptic currents (mEPSCs) and inhibitory postsynaptic currents (mIPSCs) from the same hippocampal CA1 neuron. Although the training failed to affect the amplitude of either mEPSCs or mIPSCs at 2 weeks, it increased mEPSC, but not mIPSC, amplitude at 3 weeks. At 4 weeks, the training had increased the amplitude of both mEPSCs and mIPSCs, whereas mIPSC, but not mEPSC, amplitude was increased at 8 weeks. Because early-life physiological functions can affect performance, we also evaluated sensory–motor functions together with emotional state and found adequate sensory/motor functions from infancy to adulthood. Moreover, by analyzing performance of rats in multiple hippocampal-dependent tasks, we found that the developmental changes in the performance are task dependent. Taken together, these findings delineate a critical period for learning and plastic changes at hippocampal CA1 synapses. |
format | Online Article Text |
id | pubmed-9065057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90650572022-05-04 A critical period for learning and plastic changes at hippocampal CA1 synapses Sakimoto, Yuya Shintani, Ako Yoshiura, Daiki Goshima, Makoto Kida, Hiroyuki Mitsushima, Dai Sci Rep Article Postnatal development of hippocampal function has been reported in many mammalian species, including humans. To obtain synaptic evidence, we analyzed developmental changes in plasticity after an inhibitory avoidance task in rats. Learning performance was low in infants (postnatal 2 weeks) but clearly improved from the juvenile period (3–4 weeks) to adulthood (8 weeks). One hour after the training, we prepared brain slices and sequentially recorded miniature excitatory postsynaptic currents (mEPSCs) and inhibitory postsynaptic currents (mIPSCs) from the same hippocampal CA1 neuron. Although the training failed to affect the amplitude of either mEPSCs or mIPSCs at 2 weeks, it increased mEPSC, but not mIPSC, amplitude at 3 weeks. At 4 weeks, the training had increased the amplitude of both mEPSCs and mIPSCs, whereas mIPSC, but not mEPSC, amplitude was increased at 8 weeks. Because early-life physiological functions can affect performance, we also evaluated sensory–motor functions together with emotional state and found adequate sensory/motor functions from infancy to adulthood. Moreover, by analyzing performance of rats in multiple hippocampal-dependent tasks, we found that the developmental changes in the performance are task dependent. Taken together, these findings delineate a critical period for learning and plastic changes at hippocampal CA1 synapses. Nature Publishing Group UK 2022-05-03 /pmc/articles/PMC9065057/ /pubmed/35504922 http://dx.doi.org/10.1038/s41598-022-10453-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sakimoto, Yuya Shintani, Ako Yoshiura, Daiki Goshima, Makoto Kida, Hiroyuki Mitsushima, Dai A critical period for learning and plastic changes at hippocampal CA1 synapses |
title | A critical period for learning and plastic changes at hippocampal CA1 synapses |
title_full | A critical period for learning and plastic changes at hippocampal CA1 synapses |
title_fullStr | A critical period for learning and plastic changes at hippocampal CA1 synapses |
title_full_unstemmed | A critical period for learning and plastic changes at hippocampal CA1 synapses |
title_short | A critical period for learning and plastic changes at hippocampal CA1 synapses |
title_sort | critical period for learning and plastic changes at hippocampal ca1 synapses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065057/ https://www.ncbi.nlm.nih.gov/pubmed/35504922 http://dx.doi.org/10.1038/s41598-022-10453-z |
work_keys_str_mv | AT sakimotoyuya acriticalperiodforlearningandplasticchangesathippocampalca1synapses AT shintaniako acriticalperiodforlearningandplasticchangesathippocampalca1synapses AT yoshiuradaiki acriticalperiodforlearningandplasticchangesathippocampalca1synapses AT goshimamakoto acriticalperiodforlearningandplasticchangesathippocampalca1synapses AT kidahiroyuki acriticalperiodforlearningandplasticchangesathippocampalca1synapses AT mitsushimadai acriticalperiodforlearningandplasticchangesathippocampalca1synapses AT sakimotoyuya criticalperiodforlearningandplasticchangesathippocampalca1synapses AT shintaniako criticalperiodforlearningandplasticchangesathippocampalca1synapses AT yoshiuradaiki criticalperiodforlearningandplasticchangesathippocampalca1synapses AT goshimamakoto criticalperiodforlearningandplasticchangesathippocampalca1synapses AT kidahiroyuki criticalperiodforlearningandplasticchangesathippocampalca1synapses AT mitsushimadai criticalperiodforlearningandplasticchangesathippocampalca1synapses |