You are here

Neurosci Lett DOI:10.1016/j.neulet.2013.06.016

FDG-PET imaging reveals local brain glucose utilization is altered by class I histone deacetylase inhibitors.

Publication TypeJournal Article
Year of Publication2013
AuthorsSchroeder, FA, Chonde, DB, Riley, MM, Moseley, CK, Granda, ML, Wilson, CM, Wagner, FF, Zhang, Y-L, Gale, J, Holson, EB, Haggarty, SJ, Hooker, JM
JournalNeurosci Lett
Volume550
Pages119-24
Date Published2013 Aug 29
ISSN1872-7972
KeywordsAnimals, Brain, Fluorodeoxyglucose F18, Glucose, Histone Deacetylase Inhibitors, Image Processing, Computer-Assisted, Neuroimaging, Phenylenediamines, Positron-Emission Tomography, Rats
Abstract

The purpose of this work--the first of its kind--was to evaluate the impact of chronic selective histone deacetylase (HDAC) inhibitor treatment on brain activity using uptake of the radioligand (18)F-fluorodeoxyglucose and positron emission tomography ((18)FDG-PET). HDAC dysfunction and other epigenetic mechanisms are implicated in diverse CNS disorders and animal research suggests HDAC inhibition may provide a lead toward developing improved treatment. To begin to better understand the role of the class I HDAC subtypes HDAC 1, 2 and 3 in modulating brain activity, we utilized two benzamide inhibitors from the literature, compound 60 (Cpd-60) and CI-994 which selectively inhibit HDAC 1 and 2 or HDACs 1, 2 and 3, respectively. One day after the seventh treatment with Cpd-60 (22.5 mg/kg) or CI-994 (5 mg/kg), (18)FDG-PET experiments (n=11-12 rats per treatment group) revealed significant, local changes in brain glucose utilization. These 2-17% changes were represented by increases and decreases in glucose uptake. The pattern of changes was similar but distinct between Cpd-60 and CI-994, supporting that (18)FDG-PET is a useful tool to examine the relationship between HDAC subtype activity and brain activity. Further work using additional selective HDAC inhibitors will be needed to clarify these effects as well as to understand how brain activity changes influence behavioral response.

DOI10.1016/j.neulet.2013.06.016
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/23810801?dopt=Abstract

Alternate JournalNeurosci. Lett.
PubMed ID23810801
PubMed Central IDPMC3750730
Grant ListR01DA028301 / DA / NIDA NIH HHS / United States
R01DA030321 / DA / NIDA NIH HHS / United States
R01 DA030321 / DA / NIDA NIH HHS / United States
S10 RR015728 / RR / NCRR NIH HHS / United States
S10 RR023385 / RR / NCRR NIH HHS / United States
R01 DA028301 / DA / NIDA NIH HHS / United States