Ketogenic diet rescues mouse embryos missing the mitochondrial pyruvate carrier

Our SNF Sinargia work with the Martinou Lab (U. Geneva) was published in PLoS Genetics. Congratulation to his team, Petra and Manuel!

by Nicola Zamboni

Summary

The tight control of cellular metabolism and energy production plays a crucial role during embryonic development, cancer and neurodegenerative disorders. We show that mitochondrial pyruvate carrier deficiency in mice causes metabolic alterations that result in lactic acidosis, neurotransmitter imbalance, energy deficit, brain damage and embryonic lethality. Feeding the pregnant dams a ketogenic diet allowed the survival of affected embryos until birth. Our results demonstrate the importance of the mitochondrial pyruvate carrier in maintaining the metabolic program necessary to sustain normal mammalian development.

Reference

Vanderperre B, Herzig S, Krznar P, Hörl M, Ammar Z, Montessuit S, Pierredon S, Zamboni N, Martinou JC. Embryonic Lethality of Mitochondrial Pyruvate Carrier 1 Deficient Mouse Can Be Rescued by a Ketogenic DietPLoS Genetics, 2016; 12(5):e1006056. external pagePubmed doi:external page10.1371/journal.pgen.1006056

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