Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex

Abstract Aims The molecular and cellular mechanisms underlying the antidepressant effects of fluoxetine in the brain are not fully understood. Emerging evidence has led to the hypothesis that chronic fluoxetine treatment induces dematuration of certain types of mature neurons in rodents. These studi...

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Main Authors: Hideo Hagihara, Koji Ohira, Tsuyoshi Miyakawa
Format: Article
Language:English
Published: Wiley 2019-06-01
Series:Neuropsychopharmacology Reports
Online Access:https://doi.org/10.1002/npr2.12048
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author Hideo Hagihara
Koji Ohira
Tsuyoshi Miyakawa
author_facet Hideo Hagihara
Koji Ohira
Tsuyoshi Miyakawa
author_sort Hideo Hagihara
collection DOAJ
description Abstract Aims The molecular and cellular mechanisms underlying the antidepressant effects of fluoxetine in the brain are not fully understood. Emerging evidence has led to the hypothesis that chronic fluoxetine treatment induces dematuration of certain types of mature neurons in rodents. These studies have focused on the properties of typical molecular and/or electrophysiological markers for neuronal maturation. Nevertheless, it remains unknown whether dematuration‐related phenomena are present at the genome‐wide gene expression level. Methods Based on the aforementioned hypothesis, we directly compared transcriptome data between fluoxetine‐treated adult mice and those of naive infants in the hippocampus and medial prefrontal cortex (mPFC) to assess similarities and/or differences. We further investigated whether fluoxetine treatment caused dematuration in these brain regions in a hypothesis‐free manner using a weighted gene co‐expression network analysis (WGCNA). Results Gene expression patterns in fluoxetine‐treated mice resembled those in infants in the mPFC and, to a large extent, in the hippocampus. The gene expression patterns of fluoxetine‐treated adult mice were more similar to those of approximately 2‐week‐old infants than those of older mice. WGCNA confirmed that fluoxetine treatment was associated with maturation abnormalities, particularly in the hippocampus, and highlighted respective co‐expression modules for maturity and immaturity marker genes in the hippocampus in response to fluoxetine treatment. Conclusions Our results strongly support the hypothesis that chronic fluoxetine treatment induces dematuration in the adult mouse brain from a transcriptomic standpoint. Detection of discrete transcriptomic regulatory networks related to fluoxetine treatment may help to further elucidate the mechanisms of antidepressant action.
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spelling doaj.art-34f5a11e01f342f2bf46a6aaf286ab742022-12-22T02:56:57ZengWileyNeuropsychopharmacology Reports2574-173X2019-06-01392788910.1002/npr2.12048Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortexHideo Hagihara0Koji Ohira1Tsuyoshi Miyakawa2Division of Systems Medical Science Institute for Comprehensive Medical Science Fujita Health University Toyoake JapanDivision of Systems Medical Science Institute for Comprehensive Medical Science Fujita Health University Toyoake JapanDivision of Systems Medical Science Institute for Comprehensive Medical Science Fujita Health University Toyoake JapanAbstract Aims The molecular and cellular mechanisms underlying the antidepressant effects of fluoxetine in the brain are not fully understood. Emerging evidence has led to the hypothesis that chronic fluoxetine treatment induces dematuration of certain types of mature neurons in rodents. These studies have focused on the properties of typical molecular and/or electrophysiological markers for neuronal maturation. Nevertheless, it remains unknown whether dematuration‐related phenomena are present at the genome‐wide gene expression level. Methods Based on the aforementioned hypothesis, we directly compared transcriptome data between fluoxetine‐treated adult mice and those of naive infants in the hippocampus and medial prefrontal cortex (mPFC) to assess similarities and/or differences. We further investigated whether fluoxetine treatment caused dematuration in these brain regions in a hypothesis‐free manner using a weighted gene co‐expression network analysis (WGCNA). Results Gene expression patterns in fluoxetine‐treated mice resembled those in infants in the mPFC and, to a large extent, in the hippocampus. The gene expression patterns of fluoxetine‐treated adult mice were more similar to those of approximately 2‐week‐old infants than those of older mice. WGCNA confirmed that fluoxetine treatment was associated with maturation abnormalities, particularly in the hippocampus, and highlighted respective co‐expression modules for maturity and immaturity marker genes in the hippocampus in response to fluoxetine treatment. Conclusions Our results strongly support the hypothesis that chronic fluoxetine treatment induces dematuration in the adult mouse brain from a transcriptomic standpoint. Detection of discrete transcriptomic regulatory networks related to fluoxetine treatment may help to further elucidate the mechanisms of antidepressant action.https://doi.org/10.1002/npr2.12048
spellingShingle Hideo Hagihara
Koji Ohira
Tsuyoshi Miyakawa
Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
Neuropsychopharmacology Reports
title Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
title_full Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
title_fullStr Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
title_full_unstemmed Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
title_short Transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
title_sort transcriptomic evidence for immaturity induced by antidepressant fluoxetine in the hippocampus and prefrontal cortex
url https://doi.org/10.1002/npr2.12048
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