JCI Insight · 2019 · 367 citations · 49 references
Life SciencesCardiologyPhysiologyBioenergeticsMetabolismMitochondrial BiologyCardiac PhysiologyHeart FailureKetone Body MetabolismMitochondrial BioenergeticsMitochondrial MetabolismMitochondrial PhysiologyCardiac Mitochondrial FunctionCardiac RemodelingCardiomyocyte EnergeticsFatty AcidsKetone Body OxidationKetone Body Utilization In HeartMitochondrial Fatty Acid OxidationMitochondrial Function In Cardiomyocytes
Evidence has emerged that the failing heart increases utilization of ketone bodies. We sought to determine whether this fuel shift is adaptive. Mice rendered incapable of oxidizing the ketone body 3-hydroxybutyrate (3OHB) in the heart exhibited worsened heart failure in response to fasting or a pressure overload/ischemic insult compared with WT controls. Increased delivery of 3OHB ameliorated pathologic cardiac remodeling and dysfunction in mice and in a canine pacing model of progressive heart failure. 3OHB was shown to enhance bioenergetic thermodynamics of isolated mitochondria in the context of limiting levels of fatty acids. These results indicate that the heart utilizes 3OHB as a metabolic stress defense and suggest that strategies aimed at increasing ketone delivery to the heart could prove useful in the treatment of heart failure.
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The ketone metabolite β-hydroxybutyrate blocks NLRP3 inflammasome–mediated inflammatory disease
Yun‐Hee Youm, Kim Nguyen, Ryan W. Grant et al. · Nature Medicine · 2015 · 2.1K citations · Full text
Brain Metabolism during Fasting*
O E Owen, Alfred P. Morgan, H. G. Kemp et al. · Journal of Clinical Investigation · 1967 · 1.6K citations · Full text