A ketogenic diet rescues hippocampal memory defects in a mouse model of Kabuki syndrome

作者：Benjamin Joel S; Pilarowski Genay O; Carosso Giovanni A; Zhang Li; Huso David L; Goff Loyal A; Vernon Hilary J; Hansen Kasper D; Bjornsson Hans T^*

来源：Proceedings of the National Academy of Sciences of the United States of America, 2017, 114(1): 125-130.

DOI：10.1073/pnas.1611431114

• epigenetics
• histone machinery
• adult neurogenesis
• intellectual disability
• ketone bodies

Kabuki syndrome is a Mendelian intellectual disability syndrome caused by mutations in either of two genes (KMT2D and KDM6A) involved in chromatin accessibility. We previously showed that an agent that promotes chromatin opening, the histone deacetylase inhibitor (HDACi) AR-42, ameliorates the deficiency of adult neurogenesis in the granule cell layer of the dentate gyrus and rescues hippocampal memory defects in a mouse model of Kabuki syndrome (Kmt2d(+/beta Geo)). Unlike a drug, a dietary intervention could be quickly transitioned to the clinic. Therefore, we have explored whether treatment with a ketogenic diet could lead to a similar rescue through increased amounts of beta-hydroxybutyrate, an endogenous HDACi. Here, we report that a ketogenic diet in Kmt2d(+/beta Geo) mice modulates H3ac and H3K4me3 in the granule cell layer, with concomitant rescue of both the neurogenesis defect and hippocampal memory abnormalities seen in Kmt2d(+/beta Geo) mice; similar effects on neurogenesis were observed on exogenous administration of beta-hydroxybutyrate. These data suggest that dietary modulation of epigenetic modifications through elevation of beta-hydroxybutyrate may provide a feasible strategy to treat the intellectual disability seen in Kabuki syndrome and related disorders.

• 出版日期2017-1-3