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HDAC inhibitors as cognitive enhancers in fear, anxiety and trauma therapy: where do we stand?
- Source :
- Biochemical Society Transactions
- Publication Year :
- 2014
-
Abstract
- A novel strategy to treat anxiety and fear-related disorders such as phobias, panic and PTSD (post-traumatic stress disorder) is combining CBT (cognitive behavioural therapy), including extinction-based exposure therapy, with cognitive enhancers. By targeting and boosting mechanisms underlying learning, drug development in this field aims at designing CBT-augmenting compounds that help to overcome extinction learning deficits, promote long-term fear inhibition and thus support relapse prevention. Progress in revealing the role of epigenetic regulation of specific genes associated with extinction memory generation has opened new avenues in this direction. The present review examines recent evidence from pre-clinical studies showing that increasing histone acetylation, either via genetic or pharmacological inhibition of HDACs (histone deacetylases) by e.g. vorinostat/SAHA (suberoylanilide hydroxamic acid), entinostat/MS-275, sodium butyrate, TSA (trichostatin A) or VPA (valproic acid), or by targeting HATs (histone acetyltransferases), augments fear extinction and, importantly, generates a long-term extinction memory that can protect from return of fear phenomena. The molecular mechanisms and pathways involved including BDNF (brain-derived neurotrophic factor) and NMDA (N-methyl-D-aspartate) receptor signalling are just beginning to be revealed. First studies in healthy humans are in support of extinction-facilitating effects of HDAC inhibitors. Very recent evidence that HDAC inhibitors can rescue deficits in extinction-memory-impaired rodents indicates a potential clinical utility of this approach also for exposure therapy-resistant patients. Important future work includes investigation of the long-term safety aspects of HDAC inhibitor treatment, as well as design of isotype(s)-specific inhibitors. Taken together, HDAC inhibitors display promising potential as pharmacological adjuncts to augment the efficacy of exposure-based approaches in anxiety and trauma therapy.
- Subjects :
- CS, conditioned stimulus
VPA, valproic acid
US, unconditioned stimulus
S7
histone deacetylase inhibitor (HDAC inhibitor)
histone acetyltransferase activator (HAT activator)
HDAC, histone deacetylase
Anxiety
CREB, cAMP-response-element-binding protein
SSRI, selective serotonin-re-uptake inhibitor
Humans
lysine acetylation
CBP, CREB-binding protein
Nootropic Agents
CoREST, co-repressor for element-1-silencing transcription factor
Independent Meeting
SPS, single prolonged stress
cognitive enhancer
epigenetics
NMDA, N-methyl-D-aspartate
NuRD, nucleosome remodelling and deacetylation
Fear
Histone Deacetylase Inhibitors
anxiolytic therapy
trauma
PTSD, post-traumatic stress disorder
SAHA, suberoylanilide hydroxamic acid
BDNF, brain-derived neurotrophic factor
Wounds and Injuries
HAT, histone acetyltransferase
CBT, cognitive behavioural therapy
Subjects
Details
- ISSN :
- 14708752
- Volume :
- 42
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Biochemical Society transactions
- Accession number :
- edsair.pmid..........1302ac3abbb43117d8c93b6adb42d03d