The therapeutic implications of ketone bodies: the effects of ketone bodies in pathological conditions: ketosis, ketogenic diet, redox states, insulin resistance, and mitochondrial metabolism
Veech RL · 2004 · Prostaglandins, Leukotrienes and Essential Fatty Acids
DOI: 10.1016/j.plefa.2003.09.007View source ↗
“Mild ketosis may offer therapeutic potential in a variety of different common and rare disease states.”
Summary
Richard Veech's 2004 review is the most-cited mechanistic argument that ketone bodies — specifically D-β-hydroxybutyrate — are not just an alternative fuel but a more efficient one in metabolic terms. Veech's central claim is that the enthalpy of D-β-hydroxybutyrate combustion is higher per unit oxygen consumed than glucose, meaning more ATP per oxygen molecule. He uses this thermodynamic observation to argue that mild ketosis may be therapeutically useful in conditions where mitochondrial efficiency is compromised: insulin resistance, neurodegeneration, ischemia, and certain rare metabolic disorders. The review covers redox state changes during ketosis (favorable shifts in NAD+/NADH), the role of free fatty acid elevation alongside ketones in ketogenic-diet states, and the activation of PPAR signaling. Veech's framing seeded the modern field of "exogenous ketones as therapy" and is widely cited in research on ketogenic diets for epilepsy, Alzheimer's disease, and traumatic brain injury. The therapeutic claims are speculative for many of the listed conditions; the underlying biochemistry is rigorous.
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References cited by this entry
Veech 2004 framed ketones as therapeutically useful via mitochondrial energetics; Newman/Verdin 2014 extended the framework with ketones-as-signaling-molecules (HDAC inhibition, GPCR binding) — different mechanistic angles on the same therapeutic claim.
- ExtendsThe human metabolic response to chronic ketosis without caloric restriction: preservation of submaximal exercise capability with reduced carbohydrate oxidationPhinney SD et al. · 1983
Phinney 1983 established that ketosis preserves submaximal exercise capacity in trained athletes; Veech 2004 explains the mitochondrial energetics — D-β-hydroxybutyrate has higher inherent energy content than pyruvate, the normal mitochondrial fuel from glycolysis.
Entries that reference this one
Veech 2004 builds on the brain-ketone-uptake biology characterized first by Owen and colleagues, extending it into the βHB-as-signaling-molecule literature.
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