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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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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 |
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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 |
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