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Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia
Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model of NMDA receptor hypofunction by chronically treating rats with low doses of the NMDA recep...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930128/ https://www.ncbi.nlm.nih.gov/pubmed/26460480 http://dx.doi.org/10.1038/tp.2015.151 |
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author | Ingason, A Giegling, I Hartmann, A M Genius, J Konte, B Friedl, M Ripke, S Sullivan, P F St. Clair, D Collier, D A O'Donovan, M C Mirnics, K Rujescu, D |
author_facet | Ingason, A Giegling, I Hartmann, A M Genius, J Konte, B Friedl, M Ripke, S Sullivan, P F St. Clair, D Collier, D A O'Donovan, M C Mirnics, K Rujescu, D |
author_sort | Ingason, A |
collection | PubMed |
description | Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model of NMDA receptor hypofunction by chronically treating rats with low doses of the NMDA receptor antagonist MK-801. Subsequently, we performed an expression study and identified 20 genes showing altered expression in the brain of these rats compared with untreated animals. We then explored whether the human orthologs of these genes are associated with schizophrenia in the largest schizophrenia genome-wide association study published to date, and found evidence for association for 4 out of the 20 genes: SF3B1, FOXP1, DLG2 and VGLL4. Interestingly, three of these genes, FOXP1, SF3B1 and DLG2, have previously been implicated in neurodevelopmental disorders. |
format | Online Article Text |
id | pubmed-4930128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49301282016-07-14 Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia Ingason, A Giegling, I Hartmann, A M Genius, J Konte, B Friedl, M Ripke, S Sullivan, P F St. Clair, D Collier, D A O'Donovan, M C Mirnics, K Rujescu, D Transl Psychiatry Original Article Antagonists of the N-methyl-D-aspartate (NMDA)-type glutamate receptor induce psychosis in healthy individuals and exacerbate schizophrenia symptoms in patients. In this study we have produced an animal model of NMDA receptor hypofunction by chronically treating rats with low doses of the NMDA receptor antagonist MK-801. Subsequently, we performed an expression study and identified 20 genes showing altered expression in the brain of these rats compared with untreated animals. We then explored whether the human orthologs of these genes are associated with schizophrenia in the largest schizophrenia genome-wide association study published to date, and found evidence for association for 4 out of the 20 genes: SF3B1, FOXP1, DLG2 and VGLL4. Interestingly, three of these genes, FOXP1, SF3B1 and DLG2, have previously been implicated in neurodevelopmental disorders. Nature Publishing Group 2015-10 2015-10-13 /pmc/articles/PMC4930128/ /pubmed/26460480 http://dx.doi.org/10.1038/tp.2015.151 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Ingason, A Giegling, I Hartmann, A M Genius, J Konte, B Friedl, M Ripke, S Sullivan, P F St. Clair, D Collier, D A O'Donovan, M C Mirnics, K Rujescu, D Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
title | Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
title_full | Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
title_fullStr | Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
title_full_unstemmed | Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
title_short | Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
title_sort | expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930128/ https://www.ncbi.nlm.nih.gov/pubmed/26460480 http://dx.doi.org/10.1038/tp.2015.151 |
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