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Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs
Synapsins are neuronal phosphoproteins crucial to regulating the processes required for normal neurotransmitter release. Synapsin II, in particular, has been implied as a candidate gene for schizophrenia. This study investigated synapsin II mRNA expression, using Real Time RT-PCR, in coded dorsolate...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970980/ https://www.ncbi.nlm.nih.gov/pubmed/23529008 http://dx.doi.org/10.1038/tpj.2013.6 |
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author | Tan, Mattea Dyck, Bailey A. Gabriele, Joseph Daya, Ritesh Thomas, Nancy Sookram, Christal Basu, Dipannita Ferro, Mark A. Mishra, Ram K. |
author_facet | Tan, Mattea Dyck, Bailey A. Gabriele, Joseph Daya, Ritesh Thomas, Nancy Sookram, Christal Basu, Dipannita Ferro, Mark A. Mishra, Ram K. |
author_sort | Tan, Mattea |
collection | PubMed |
description | Synapsins are neuronal phosphoproteins crucial to regulating the processes required for normal neurotransmitter release. Synapsin II, in particular, has been implied as a candidate gene for schizophrenia. This study investigated synapsin II mRNA expression, using Real Time RT-PCR, in coded dorsolateral prefrontal cortical samples provided by the Stanley Foundation Neuropathology Consortium. Synapsin IIa was decreased in patients with schizophrenia when compared to both healthy subjects and patients with bipolar disorder, whereas the synapsin IIb was only significantly reduced in patients with schizophrenia when compared to healthy subjects, but not patients with bipolar disorder. Furthermore, lifetime antipsychotic drug use was positively associated with synapsin IIa expression in patients with schizophrenia. Results suggest that impairment of synaptic transmission by synapsin II reduction may contribute to dysregulated convergent molecular mechanisms which result in aberrant neural circuits that characterize schizophrenia, while implicating involvement of synapsin II in therapeutic mechanisms of currently prescribed antipsychotic drugs. |
format | Online Article Text |
id | pubmed-3970980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-39709802014-08-01 Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs Tan, Mattea Dyck, Bailey A. Gabriele, Joseph Daya, Ritesh Thomas, Nancy Sookram, Christal Basu, Dipannita Ferro, Mark A. Mishra, Ram K. Pharmacogenomics J Article Synapsins are neuronal phosphoproteins crucial to regulating the processes required for normal neurotransmitter release. Synapsin II, in particular, has been implied as a candidate gene for schizophrenia. This study investigated synapsin II mRNA expression, using Real Time RT-PCR, in coded dorsolateral prefrontal cortical samples provided by the Stanley Foundation Neuropathology Consortium. Synapsin IIa was decreased in patients with schizophrenia when compared to both healthy subjects and patients with bipolar disorder, whereas the synapsin IIb was only significantly reduced in patients with schizophrenia when compared to healthy subjects, but not patients with bipolar disorder. Furthermore, lifetime antipsychotic drug use was positively associated with synapsin IIa expression in patients with schizophrenia. Results suggest that impairment of synaptic transmission by synapsin II reduction may contribute to dysregulated convergent molecular mechanisms which result in aberrant neural circuits that characterize schizophrenia, while implicating involvement of synapsin II in therapeutic mechanisms of currently prescribed antipsychotic drugs. 2013-03-26 2014-02 /pmc/articles/PMC3970980/ /pubmed/23529008 http://dx.doi.org/10.1038/tpj.2013.6 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Tan, Mattea Dyck, Bailey A. Gabriele, Joseph Daya, Ritesh Thomas, Nancy Sookram, Christal Basu, Dipannita Ferro, Mark A. Mishra, Ram K. Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs |
title | Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs |
title_full | Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs |
title_fullStr | Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs |
title_full_unstemmed | Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs |
title_short | Synapsin II Gene Expression in the Dorsolateral Prefrontal Cortex of Brain Specimens from Patients with Schizophrenia and Bipolar Disorder: Effect of Lifetime Intake of Antipsychotic Drugs |
title_sort | synapsin ii gene expression in the dorsolateral prefrontal cortex of brain specimens from patients with schizophrenia and bipolar disorder: effect of lifetime intake of antipsychotic drugs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970980/ https://www.ncbi.nlm.nih.gov/pubmed/23529008 http://dx.doi.org/10.1038/tpj.2013.6 |
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