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Ketone ester effects on metabolism and transcription

Journal

JOURNAL OF LIPID RESEARCH
Volume 55, Issue 10, Pages 2004-2006

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ELSEVIER
DOI: 10.1194/jlr.R046292

Keywords

D-beta-hydroxybutyrate - R-1,3 butanediol monoester; elevated blood ketones; Alzheimer's disease; antioxidants; diabetes; fatty acid; deacetylase; ketosis

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Ketosis induced by starvation or feeding a ketogenic diet has widespread and often contradictory effects due to the simultaneous elevation of both ketone bodies and free fatty acids. The elevation of ketone bodies increases the energy of ATP hydrolysis by reducing the mitochondrial NAD couple and oxidizing the coenzyme Q couple, thus increasing the redox span between site I and site II. In contrast, metabolism of fatty acids leads to a reduction of both mitochondrial NAD and mitochondrial coenzyme Q causing a decrease in the Delta G of ATP hydrolysis. In contrast, feeding ketone body esters leads to pure ketosis, unaccompanied by elevation of free fatty acids, producing a physiological state not previously seen in nature. The effects of pure ketosis on transcription and upon certain neurodegenerative diseases make approach not only interesting, but of potential therapeutic value.

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