Selective boosting of transcriptional and behavioral responses to drugs of abuse by histone deacetylase inhibition - PubMed (original) (raw)
. 2009 Dec;34(13):2642-54.
doi: 10.1038/npp.2009.125. Epub 2009 Sep 2.
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- PMID: 19727068
- DOI: 10.1038/npp.2009.125
Free article
Selective boosting of transcriptional and behavioral responses to drugs of abuse by histone deacetylase inhibition
Carles Sanchis-Segura et al. Neuropsychopharmacology. 2009 Dec.
Free article
Abstract
Histone acetylation and other modifications of the chromatin are important regulators of gene expression and, consequently, may contribute to drug-induced behaviors and neuroplasticity. Earlier studies have shown that a reduction in histone deacetylase (HDAC) activity results in the enhancement of some psychostimulant-induced behaviors. In this study, we extend those seminal findings by showing that the administration of the HDAC inhibitor sodium butyrate enhances morphine-induced locomotor sensitization and conditioned place preference. In contrast, this compound has no effects on the development of morphine tolerance and dependence. Similar effects were observed for cocaine and ethanol-induced behaviors. These behavioral changes were accompanied by a selective boosting of a component of the transcriptional program activated by chronic morphine administration that included circadian clock genes and other genes relevant to addictive behavior. Our results support a specific function for histone acetylation and the epigenetic modulation of transcription at a reduced number of biologically relevant loci on non-homeostatic, long-lasting, drug-induced behavioral plasticity.
Comment in
- Synergistic interactions between histone deacetylase inhibitors and drugs of abuse.
Adachi M, Monteggia LM. Adachi M, et al. Neuropsychopharmacology. 2009 Dec;34(13):2619-20. doi: 10.1038/npp.2009.156. Epub 2009 Sep 30. Neuropsychopharmacology. 2009. PMID: 19794404 Free PMC article. No abstract available. - Epigenetic modifications: significance in drug addiction and treatment.
Ma L. Ma L. Epigenomics. 2010 Apr;2(2):183-6. doi: 10.2217/epi.10.15. Epigenomics. 2010. PMID: 22121869 No abstract available.
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