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Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices

Although activity-dependent transcription represents a crucial mechanism for long-lasting experience-dependent changes in the hippocampus, limited data exist on its contribution to pathological conditions. We aim to investigate the influence of chronic stress on the activity-dependent transcription...

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Autores principales: Molteni, Raffaella, Rossetti, Andrea C., Savino, Elisa, Racagni, Giorgio, Calabrese, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736009/
https://www.ncbi.nlm.nih.gov/pubmed/26881097
http://dx.doi.org/10.1155/2016/2592319
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author Molteni, Raffaella
Rossetti, Andrea C.
Savino, Elisa
Racagni, Giorgio
Calabrese, Francesca
author_facet Molteni, Raffaella
Rossetti, Andrea C.
Savino, Elisa
Racagni, Giorgio
Calabrese, Francesca
author_sort Molteni, Raffaella
collection PubMed
description Although activity-dependent transcription represents a crucial mechanism for long-lasting experience-dependent changes in the hippocampus, limited data exist on its contribution to pathological conditions. We aim to investigate the influence of chronic stress on the activity-dependent transcription of brain-derived neurotrophic factor (BDNF). The ex vivo methodology of acute stimulation of hippocampal slices obtained from rats exposed to chronic mild stress (CMS) was used to evaluate whether the adverse experience may alter activity-dependent BDNF gene expression. CMS reduces BDNF expression and that acute depolarization significantly upregulates total BDNF mRNA levels only in control animals, showing that CMS exposure may alter BDNF transcription under basal conditions and during neuronal activation. Moreover, while the basal effect of CMS on total BDNF reflects parallel modulations of all the transcripts examined, isoform-specific changes were found after depolarization. This different effect was also observed in the activation of intracellular signaling pathways related to the neurotrophin. In conclusion, our study discloses a functional alteration of BDNF transcription as a consequence of stress. Being the activity-regulated transcription a critical process in synaptic and neuronal plasticity, the different regulation of individual BDNF promoters may contribute to long-lasting changes, which are fundamental for the vulnerability of the hippocampus to stress-related diseases.
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spelling pubmed-47360092016-02-15 Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices Molteni, Raffaella Rossetti, Andrea C. Savino, Elisa Racagni, Giorgio Calabrese, Francesca Neural Plast Research Article Although activity-dependent transcription represents a crucial mechanism for long-lasting experience-dependent changes in the hippocampus, limited data exist on its contribution to pathological conditions. We aim to investigate the influence of chronic stress on the activity-dependent transcription of brain-derived neurotrophic factor (BDNF). The ex vivo methodology of acute stimulation of hippocampal slices obtained from rats exposed to chronic mild stress (CMS) was used to evaluate whether the adverse experience may alter activity-dependent BDNF gene expression. CMS reduces BDNF expression and that acute depolarization significantly upregulates total BDNF mRNA levels only in control animals, showing that CMS exposure may alter BDNF transcription under basal conditions and during neuronal activation. Moreover, while the basal effect of CMS on total BDNF reflects parallel modulations of all the transcripts examined, isoform-specific changes were found after depolarization. This different effect was also observed in the activation of intracellular signaling pathways related to the neurotrophin. In conclusion, our study discloses a functional alteration of BDNF transcription as a consequence of stress. Being the activity-regulated transcription a critical process in synaptic and neuronal plasticity, the different regulation of individual BDNF promoters may contribute to long-lasting changes, which are fundamental for the vulnerability of the hippocampus to stress-related diseases. Hindawi Publishing Corporation 2016 2015-12-31 /pmc/articles/PMC4736009/ /pubmed/26881097 http://dx.doi.org/10.1155/2016/2592319 Text en Copyright © 2016 Raffaella Molteni et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Molteni, Raffaella
Rossetti, Andrea C.
Savino, Elisa
Racagni, Giorgio
Calabrese, Francesca
Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices
title Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices
title_full Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices
title_fullStr Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices
title_full_unstemmed Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices
title_short Chronic Mild Stress Modulates Activity-Dependent Transcription of BDNF in Rat Hippocampal Slices
title_sort chronic mild stress modulates activity-dependent transcription of bdnf in rat hippocampal slices
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736009/
https://www.ncbi.nlm.nih.gov/pubmed/26881097
http://dx.doi.org/10.1155/2016/2592319
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