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Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility
In recent years it has become clear that corticosteroid hormones (such as corticosterone) are released in ultradian pulses as a natural consequence of pituitary-adrenal interactions. All organs, including the brain, are thus exposed to pulsatile changes in corticosteroid hormone level, important to...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712151/ https://www.ncbi.nlm.nih.gov/pubmed/26741493 http://dx.doi.org/10.1371/journal.pone.0145858 |
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author | Sarabdjitsingh, R. Angela Pasricha, Natasha Smeets, Johanna A. S. Kerkhofs, Amber Mikasova, Lenka Karst, Henk Groc, Laurent Joëls, Marian |
author_facet | Sarabdjitsingh, R. Angela Pasricha, Natasha Smeets, Johanna A. S. Kerkhofs, Amber Mikasova, Lenka Karst, Henk Groc, Laurent Joëls, Marian |
author_sort | Sarabdjitsingh, R. Angela |
collection | PubMed |
description | In recent years it has become clear that corticosteroid hormones (such as corticosterone) are released in ultradian pulses as a natural consequence of pituitary-adrenal interactions. All organs, including the brain, are thus exposed to pulsatile changes in corticosteroid hormone level, important to ensure full genomic responsiveness to stress-induced surges. However, corticosterone also changes neuronal excitability through rapid non-genomic pathways, particularly in the hippocampus. Potentially, background excitability of hippocampal neurons could thus be changed by pulsatile exposure to corticosteroids. It is currently unknown, though, how neuronal activity alters during a sequence of corticosterone pulses. To test this, hippocampal cells were exposed in vitro to four consecutive corticosterone pulses with a 60 min inter-pulse interval. During the pulses we examined four features of hippocampal signal transfer by the main excitatory transmitter glutamate—i.e., postsynaptic responses to spontaneous release of presynaptic vesicles, postsynaptic GluA2-AMPA receptor dynamics, basal (evoked) field responses, and synaptic plasticity, using a set of high resolution imaging and electrophysiological approaches. We show that the first pulse of corticosterone causes a transient increase in miniature EPSC frequency, AMPA receptor trafficking and synaptic plasticity, while basal evoked field responses are unaffected. This pattern is not maintained during subsequent applications: responses become more variable, attenuate or even reverse over time, albeit with different kinetics for the various experimental endpoints. This may indicate that the beneficial effect of ultradian pulses on transcriptional regulation in the hippocampus is not consistently accompanied by short-term perturbations in background excitability. In general, this could be interpreted as a means to keep hippocampal neurons responsive to incoming signals related to environmental challenges. |
format | Online Article Text |
id | pubmed-4712151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47121512016-01-26 Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility Sarabdjitsingh, R. Angela Pasricha, Natasha Smeets, Johanna A. S. Kerkhofs, Amber Mikasova, Lenka Karst, Henk Groc, Laurent Joëls, Marian PLoS One Research Article In recent years it has become clear that corticosteroid hormones (such as corticosterone) are released in ultradian pulses as a natural consequence of pituitary-adrenal interactions. All organs, including the brain, are thus exposed to pulsatile changes in corticosteroid hormone level, important to ensure full genomic responsiveness to stress-induced surges. However, corticosterone also changes neuronal excitability through rapid non-genomic pathways, particularly in the hippocampus. Potentially, background excitability of hippocampal neurons could thus be changed by pulsatile exposure to corticosteroids. It is currently unknown, though, how neuronal activity alters during a sequence of corticosterone pulses. To test this, hippocampal cells were exposed in vitro to four consecutive corticosterone pulses with a 60 min inter-pulse interval. During the pulses we examined four features of hippocampal signal transfer by the main excitatory transmitter glutamate—i.e., postsynaptic responses to spontaneous release of presynaptic vesicles, postsynaptic GluA2-AMPA receptor dynamics, basal (evoked) field responses, and synaptic plasticity, using a set of high resolution imaging and electrophysiological approaches. We show that the first pulse of corticosterone causes a transient increase in miniature EPSC frequency, AMPA receptor trafficking and synaptic plasticity, while basal evoked field responses are unaffected. This pattern is not maintained during subsequent applications: responses become more variable, attenuate or even reverse over time, albeit with different kinetics for the various experimental endpoints. This may indicate that the beneficial effect of ultradian pulses on transcriptional regulation in the hippocampus is not consistently accompanied by short-term perturbations in background excitability. In general, this could be interpreted as a means to keep hippocampal neurons responsive to incoming signals related to environmental challenges. Public Library of Science 2016-01-07 /pmc/articles/PMC4712151/ /pubmed/26741493 http://dx.doi.org/10.1371/journal.pone.0145858 Text en © 2016 Sarabdjitsingh et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Research Article Sarabdjitsingh, R. Angela Pasricha, Natasha Smeets, Johanna A. S. Kerkhofs, Amber Mikasova, Lenka Karst, Henk Groc, Laurent Joëls, Marian Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility |
title | Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility |
title_full | Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility |
title_fullStr | Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility |
title_full_unstemmed | Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility |
title_short | Hippocampal Fast Glutamatergic Transmission Is Transiently Regulated by Corticosterone Pulsatility |
title_sort | hippocampal fast glutamatergic transmission is transiently regulated by corticosterone pulsatility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712151/ https://www.ncbi.nlm.nih.gov/pubmed/26741493 http://dx.doi.org/10.1371/journal.pone.0145858 |
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