Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5844297 | Progress in Neuro-Psychopharmacology and Biological Psychiatry | 2016 | 5 Pages |
Abstract
Numerous preclinical studies demonstrate that changes in gene expression in the brain occur in animal models of depression using exposure to stress, such as social defeat and leaned helplessness, and that repeated administration of antidepressants ameliorates these stress-induced changes in gene expression. These findings suggest that alteration in gene transcription in the central nervous system in response to stress plays an important role in the pathophysiology of depression. Recent advances in epigenetics have led to the realization that chromatin remodeling mediated by histone deacetylase (HDAC) is closely involved in the regulation of gene transcription. In this context, we first review several preclinical studies demonstrating the antidepressant-like efficacy of HDAC inhibitors. We then suggest the efficacy of HDAC inhibitors in treatment-resistant depression based on the mechanism of action of HDAC. Finally, we discuss the possibility of using HDAC inhibitors in patients with treatment-resistant depression.
Keywords
CREBcAMP response binding proteinVLONACTSTHDAChistone deacetylase (HDAC) inhibitorSAHASNRIGDNFFSTVPASIRTBDNFTail suspension testforced swim testPosttraumatic stress disorderPTSDDepressionSodium butyrateAntidepressantVascular endothelial growth factorBrain-derived neurotrophic factor (BDNF)Glial cell line-derived neurotrophic factorBrain-derived neurotrophic factorVentrolateral orbital cortexSelective serotonin reuptake inhibitorSSRINADNucleus accumbensHistone acetyltransferasehistone deacetylaseValproic acidHAT
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Authors
Manabu Fuchikami, Shigeto Yamamoto, Shigeru Morinobu, Satoshi Okada, Yosuke Yamawaki, Shigeto Yamawaki,