The Class I HDAC inhibitor RGFP963 enhances consolidation of cued fear extinction.

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Behavioral Neuroscience and Psychiatric Disorders, Emory University, Atlanta, Georgia 30329, USA Howard Hughes Medical Institute, Chevy Chase, Maryland 20815, USA

Published: April 2015

Evidence indicates that broad, nonspecific histone deacetylase (HDAC) inhibition enhances learning and memory, however, the contribution of the various HDACs to specific forms of learning is incompletely understood. Here, we show that the Class I HDAC inhibitor, RGFP963, enhances consolidation of cued fear extinction. However, RGFP966, a strong inhibitor of HDAC3, does not significantly enhance consolidation of cued fear extinction. These data extend previous evidence that demonstrate the Class I HDACs play a role in the consolidation of long-term memory, suggesting that HDAC1 and/or HDAC2, but less likely HDAC3, may function as negative regulators of extinction retention. The development of specific HDAC inhibitors, such as RGFP963, will further illuminate the role of specific HDACs in various types of learning and memory. Moreover, HDAC inhibitors that enhance cued fear extinction may show translational promise for the treatment of fear-related disorders, including post-traumatic stress disorder (PTSD).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371170PMC
http://dx.doi.org/10.1101/lm.036699.114DOI Listing

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