The ketone body β-hydroxybutyrate (βHB) rescues behavioral defects in DAF-18/PTEN mutants of C. elegans

RAYES, D.; GIUNTI, S.; DE ROSA, M.J.

Congreso; XXXVI Anual meeting SAN; 2021

Mutations in the phosphatase and tensin homolog (PTEN) gene, a negative regulator of the Akt/PKB pathway,are associated with neurodevelopmental disorders (NDDs). In recent years, ketogenic diets (KGDs) have beenshown to have beneficial behavioral effects in animal models of NDDs. Ketogenic diets trigger a metabolic shiftby forcing the production of ketone bodies (KBs) to generate ATP. The mechanisms underlying the beneficialeffects of KGDs on NDDs are unknown. Here we used daf-18/PTEN mutants of C. elegans to gain molecularand cellular insights into the effects of KGDs on neurodevelopment. We find that these mutants are defective inexerting a complex behavior such as the escape response. These behavioral defects improve in animals culturedin the presence of KB β-hydroxybutyrate (βHB). Surprisingly, exposure to βHB at early stages is sufficient toachieve this improvement throughout adulthood, suggesting that βHB is necessary at a critical stage ofdevelopment. We have also found that the effect of βHB is abolished in daf-16/FOXO mutants, revealing a keyrole for this transcription factor. Finally, we observed morphological defects in GABAergic motor neurons indaf-18 mutants. We are exploring whether exposure to βHB can amend these abnormalities. Given the highlevel of conservation of the pathways involved (PTEN/AKT/FOXO) across the animal kingdom, this work couldcontribute to better understand NDDs and establishing potential therapeutic options in mammals.