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Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants

BACKGROUND: The neurotrophin BDNF has been implicated in the regulation of neuroplasticity, gene expression, and synaptic function in the adult brain, as well as in the pathophysiology of neuropsychiatric disorders and the mechanism of action of antidepressants. Antidepressant treatments have been s...

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Autores principales: Musazzi, Laura, Cattaneo, Annamaria, Tardito, Daniela, Barbon, Alessandro, Gennarelli, Massimo, Barlati, Sergio, Racagni, Giorgio, Popoli, Maurizio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689227/
https://www.ncbi.nlm.nih.gov/pubmed/19439074
http://dx.doi.org/10.1186/1471-2202-10-48
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author Musazzi, Laura
Cattaneo, Annamaria
Tardito, Daniela
Barbon, Alessandro
Gennarelli, Massimo
Barlati, Sergio
Racagni, Giorgio
Popoli, Maurizio
author_facet Musazzi, Laura
Cattaneo, Annamaria
Tardito, Daniela
Barbon, Alessandro
Gennarelli, Massimo
Barlati, Sergio
Racagni, Giorgio
Popoli, Maurizio
author_sort Musazzi, Laura
collection PubMed
description BACKGROUND: The neurotrophin BDNF has been implicated in the regulation of neuroplasticity, gene expression, and synaptic function in the adult brain, as well as in the pathophysiology of neuropsychiatric disorders and the mechanism of action of antidepressants. Antidepressant treatments have been shown to increase the expression of BDNF mRNA, although the changes measured were found to be different depending on various factors. A few studies only have measured levels of BDNF protein after antidepressant treatments, and poor correlation was found between mRNA and protein changes. We studied the time course of expression of BDNF mRNA and protein during drug treatments, in order to elucidate the temporal profile of regulation of this effector and whether mRNA and protein levels correlate. Rat groups were treated for 1, 2 or 3 weeks with fluoxetine or reboxetine; in additional groups drug treatment was followed by a washout week (3+1). Total BDNF mRNA was measured by Real Time PCR, pro- and mature BDNF proteins were measured by Western blot. RESULTS: We found that mature BDNF protein is induced more rapidly than mRNA, by both drugs in hippocampus (weeks 1–2) and by reboxetine in prefrontal/frontal cortex (week 1). The temporal profile of BDNF protein expression was largely inconsistent with that of mRNA, which followed the protein induction and reached a peak at week 3. CONCLUSION: These results suggest that BDNF protein is rapidly elevated by antidepressant treatments by posttranscriptional mechanisms, and that induction of BDNF mRNA is a slower process.
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spelling pubmed-26892272009-06-02 Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants Musazzi, Laura Cattaneo, Annamaria Tardito, Daniela Barbon, Alessandro Gennarelli, Massimo Barlati, Sergio Racagni, Giorgio Popoli, Maurizio BMC Neurosci Research Article BACKGROUND: The neurotrophin BDNF has been implicated in the regulation of neuroplasticity, gene expression, and synaptic function in the adult brain, as well as in the pathophysiology of neuropsychiatric disorders and the mechanism of action of antidepressants. Antidepressant treatments have been shown to increase the expression of BDNF mRNA, although the changes measured were found to be different depending on various factors. A few studies only have measured levels of BDNF protein after antidepressant treatments, and poor correlation was found between mRNA and protein changes. We studied the time course of expression of BDNF mRNA and protein during drug treatments, in order to elucidate the temporal profile of regulation of this effector and whether mRNA and protein levels correlate. Rat groups were treated for 1, 2 or 3 weeks with fluoxetine or reboxetine; in additional groups drug treatment was followed by a washout week (3+1). Total BDNF mRNA was measured by Real Time PCR, pro- and mature BDNF proteins were measured by Western blot. RESULTS: We found that mature BDNF protein is induced more rapidly than mRNA, by both drugs in hippocampus (weeks 1–2) and by reboxetine in prefrontal/frontal cortex (week 1). The temporal profile of BDNF protein expression was largely inconsistent with that of mRNA, which followed the protein induction and reached a peak at week 3. CONCLUSION: These results suggest that BDNF protein is rapidly elevated by antidepressant treatments by posttranscriptional mechanisms, and that induction of BDNF mRNA is a slower process. BioMed Central 2009-05-13 /pmc/articles/PMC2689227/ /pubmed/19439074 http://dx.doi.org/10.1186/1471-2202-10-48 Text en Copyright © 2009 Musazzi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Musazzi, Laura
Cattaneo, Annamaria
Tardito, Daniela
Barbon, Alessandro
Gennarelli, Massimo
Barlati, Sergio
Racagni, Giorgio
Popoli, Maurizio
Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
title Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
title_full Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
title_fullStr Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
title_full_unstemmed Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
title_short Early raise of BDNF in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
title_sort early raise of bdnf in hippocampus suggests induction of posttranscriptional mechanisms by antidepressants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689227/
https://www.ncbi.nlm.nih.gov/pubmed/19439074
http://dx.doi.org/10.1186/1471-2202-10-48
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