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Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats

Recent studies have shown that antipsychotic drugs have epigenetic effects. However, the effects of antipsychotic drugs on histone modification remain unclear. Therefore, we investigated the effects of antipsychotic drugs on the epigenetic modification of the BDNF gene in the rat hippocampus. Rats w...

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Autores principales: Seo, Mi Kyoung, Kim, Young Hoon, McIntyre, Roger S., Mansur, Rodrigo B., Lee, Yena, Carmona, Nicole E., Choi, Ah Jeong, Kim, Gyung-Mee, Lee, Jung Goo, Park, Sung Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016229/
https://www.ncbi.nlm.nih.gov/pubmed/29991943
http://dx.doi.org/10.1155/2018/2682037
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author Seo, Mi Kyoung
Kim, Young Hoon
McIntyre, Roger S.
Mansur, Rodrigo B.
Lee, Yena
Carmona, Nicole E.
Choi, Ah Jeong
Kim, Gyung-Mee
Lee, Jung Goo
Park, Sung Woo
author_facet Seo, Mi Kyoung
Kim, Young Hoon
McIntyre, Roger S.
Mansur, Rodrigo B.
Lee, Yena
Carmona, Nicole E.
Choi, Ah Jeong
Kim, Gyung-Mee
Lee, Jung Goo
Park, Sung Woo
author_sort Seo, Mi Kyoung
collection PubMed
description Recent studies have shown that antipsychotic drugs have epigenetic effects. However, the effects of antipsychotic drugs on histone modification remain unclear. Therefore, we investigated the effects of antipsychotic drugs on the epigenetic modification of the BDNF gene in the rat hippocampus. Rats were subjected to chronic restraint stress (6 h/d for 21 d) and then were administered with either olanzapine (2 mg/kg) or haloperidol (1 mg/kg). The levels of histone H3 acetylation and MeCP2 binding at BDNF promoter IV were assessed with chromatin immunoprecipitation assays. The mRNA levels of total BDNF with exon IV, HDAC5, DNMT1, and DNMT3a were assessed with a quantitative RT-PCR procedure. Chronic restraint stress resulted in the downregulation of total and exon IV BDNF mRNA levels and a decrease in histone H3 acetylation and an increase in MeCP2 binding at BDNF promoter IV. Furthermore, there were robust increases in the expression of HDAC5 and DNMTs. Olanzapine administration largely prevented these changes. The administration of haloperidol had no effect. These findings suggest that the antipsychotic drug olanzapine induced histone modification of BDNF gene expression in the hippocampus and that these epigenetic alterations may represent one of the mechanisms underlying the actions of antipsychotic drugs.
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spelling pubmed-60162292018-07-10 Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats Seo, Mi Kyoung Kim, Young Hoon McIntyre, Roger S. Mansur, Rodrigo B. Lee, Yena Carmona, Nicole E. Choi, Ah Jeong Kim, Gyung-Mee Lee, Jung Goo Park, Sung Woo Neural Plast Research Article Recent studies have shown that antipsychotic drugs have epigenetic effects. However, the effects of antipsychotic drugs on histone modification remain unclear. Therefore, we investigated the effects of antipsychotic drugs on the epigenetic modification of the BDNF gene in the rat hippocampus. Rats were subjected to chronic restraint stress (6 h/d for 21 d) and then were administered with either olanzapine (2 mg/kg) or haloperidol (1 mg/kg). The levels of histone H3 acetylation and MeCP2 binding at BDNF promoter IV were assessed with chromatin immunoprecipitation assays. The mRNA levels of total BDNF with exon IV, HDAC5, DNMT1, and DNMT3a were assessed with a quantitative RT-PCR procedure. Chronic restraint stress resulted in the downregulation of total and exon IV BDNF mRNA levels and a decrease in histone H3 acetylation and an increase in MeCP2 binding at BDNF promoter IV. Furthermore, there were robust increases in the expression of HDAC5 and DNMTs. Olanzapine administration largely prevented these changes. The administration of haloperidol had no effect. These findings suggest that the antipsychotic drug olanzapine induced histone modification of BDNF gene expression in the hippocampus and that these epigenetic alterations may represent one of the mechanisms underlying the actions of antipsychotic drugs. Hindawi 2018-06-11 /pmc/articles/PMC6016229/ /pubmed/29991943 http://dx.doi.org/10.1155/2018/2682037 Text en Copyright © 2018 Mi Kyoung Seo et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Seo, Mi Kyoung
Kim, Young Hoon
McIntyre, Roger S.
Mansur, Rodrigo B.
Lee, Yena
Carmona, Nicole E.
Choi, Ah Jeong
Kim, Gyung-Mee
Lee, Jung Goo
Park, Sung Woo
Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats
title Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats
title_full Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats
title_fullStr Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats
title_full_unstemmed Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats
title_short Effects of Antipsychotic Drugs on the Epigenetic Modification of Brain-Derived Neurotrophic Factor Gene Expression in the Hippocampi of Chronic Restraint Stress Rats
title_sort effects of antipsychotic drugs on the epigenetic modification of brain-derived neurotrophic factor gene expression in the hippocampi of chronic restraint stress rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016229/
https://www.ncbi.nlm.nih.gov/pubmed/29991943
http://dx.doi.org/10.1155/2018/2682037
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