Cargando…

Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia

The central serotonergic system is implicated in the pathogenesis of schizophrenia, where the imbalance between dopamine, serotonin and glutamate plays a key pathophysiological role. The dorsal raphe nucleus (DRN) is the main source of serotonergic innervation of forebrain limbic structures disturbe...

Descripción completa

Detalles Bibliográficos
Autores principales: Krzyżanowska, Marta, Steiner, Johann, Brisch, Ralf, Mawrin, Christian, Busse, Stefan, Braun, Katharina, Jankowski, Zbigniew, Bernstein, Hans-Gert, Bogerts, Bernhard, Gos, Tomasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339493/
https://www.ncbi.nlm.nih.gov/pubmed/25091423
http://dx.doi.org/10.1007/s00406-014-0518-4
_version_ 1782358878055301120
author Krzyżanowska, Marta
Steiner, Johann
Brisch, Ralf
Mawrin, Christian
Busse, Stefan
Braun, Katharina
Jankowski, Zbigniew
Bernstein, Hans-Gert
Bogerts, Bernhard
Gos, Tomasz
author_facet Krzyżanowska, Marta
Steiner, Johann
Brisch, Ralf
Mawrin, Christian
Busse, Stefan
Braun, Katharina
Jankowski, Zbigniew
Bernstein, Hans-Gert
Bogerts, Bernhard
Gos, Tomasz
author_sort Krzyżanowska, Marta
collection PubMed
description The central serotonergic system is implicated in the pathogenesis of schizophrenia, where the imbalance between dopamine, serotonin and glutamate plays a key pathophysiological role. The dorsal raphe nucleus (DRN) is the main source of serotonergic innervation of forebrain limbic structures disturbed in schizophrenia patients. The study was carried out on paraffin-embedded brains from 17 (8 paranoid and 9 residual) schizophrenia patients and 28 matched controls without mental disorders. The transcriptional activity of ribosomal DNA (rDNA) in DRN neurons was evaluated by the AgNOR silver-staining method. An increased rDNA transcriptional activity was found in schizophrenia patients in the cumulative analysis of all DRN subnuclei (t test, P = 0.02). Further subgroup analysis revealed that it was an effect specific for residual schizophrenia versus paranoid schizophrenia or control groups (ANOVA, P = 0.002). This effect was confounded neither by suicide nor by antipsychotic medication. Our findings suggest that increased activity of rDNA in DRN neurons is a distinct phenomenon in schizophrenia, particularly in residual patients. An activation of the rDNA transcription in DRN neurons may represent a compensatory mechanism to overcome the previously described prefrontal serotonergic hypofunction in this diagnostic subgroup.
format Online
Article
Text
id pubmed-4339493
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-43394932015-03-02 Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia Krzyżanowska, Marta Steiner, Johann Brisch, Ralf Mawrin, Christian Busse, Stefan Braun, Katharina Jankowski, Zbigniew Bernstein, Hans-Gert Bogerts, Bernhard Gos, Tomasz Eur Arch Psychiatry Clin Neurosci Original Paper The central serotonergic system is implicated in the pathogenesis of schizophrenia, where the imbalance between dopamine, serotonin and glutamate plays a key pathophysiological role. The dorsal raphe nucleus (DRN) is the main source of serotonergic innervation of forebrain limbic structures disturbed in schizophrenia patients. The study was carried out on paraffin-embedded brains from 17 (8 paranoid and 9 residual) schizophrenia patients and 28 matched controls without mental disorders. The transcriptional activity of ribosomal DNA (rDNA) in DRN neurons was evaluated by the AgNOR silver-staining method. An increased rDNA transcriptional activity was found in schizophrenia patients in the cumulative analysis of all DRN subnuclei (t test, P = 0.02). Further subgroup analysis revealed that it was an effect specific for residual schizophrenia versus paranoid schizophrenia or control groups (ANOVA, P = 0.002). This effect was confounded neither by suicide nor by antipsychotic medication. Our findings suggest that increased activity of rDNA in DRN neurons is a distinct phenomenon in schizophrenia, particularly in residual patients. An activation of the rDNA transcription in DRN neurons may represent a compensatory mechanism to overcome the previously described prefrontal serotonergic hypofunction in this diagnostic subgroup. Springer Berlin Heidelberg 2014-08-05 2015 /pmc/articles/PMC4339493/ /pubmed/25091423 http://dx.doi.org/10.1007/s00406-014-0518-4 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Krzyżanowska, Marta
Steiner, Johann
Brisch, Ralf
Mawrin, Christian
Busse, Stefan
Braun, Katharina
Jankowski, Zbigniew
Bernstein, Hans-Gert
Bogerts, Bernhard
Gos, Tomasz
Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
title Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
title_full Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
title_fullStr Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
title_full_unstemmed Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
title_short Ribosomal DNA transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
title_sort ribosomal dna transcription in the dorsal raphe nucleus is increased in residual but not in paranoid schizophrenia
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339493/
https://www.ncbi.nlm.nih.gov/pubmed/25091423
http://dx.doi.org/10.1007/s00406-014-0518-4
work_keys_str_mv AT krzyzanowskamarta ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT steinerjohann ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT brischralf ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT mawrinchristian ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT bussestefan ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT braunkatharina ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT jankowskizbigniew ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT bernsteinhansgert ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT bogertsbernhard ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia
AT gostomasz ribosomaldnatranscriptioninthedorsalraphenucleusisincreasedinresidualbutnotinparanoidschizophrenia