4.7 Article

Ketogenic diet metabolites reduce firing in central neurons by opening KATP channels

Journal

JOURNAL OF NEUROSCIENCE
Volume 27, Issue 14, Pages 3618-3625

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0132-07.2007

Keywords

epilepsy; ketogenic diet; K(ATP) channels; substantia nigra pars reticulata; glycolysis; anticonvulsant treatment

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Funding

  1. NINDS NIH HHS [F31 NS048798] Funding Source: Medline

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A low-carbohydrate ketogenic diet remains one of the most effective (but mysterious) treatments for severe pharmacoresistant epilepsy. We have tested for an acute effect of physiological ketone bodies on neuronal firing rates and excitability, to discover possible therapeutic mechanisms of the ketogenic diet. Physiological concentrations of ketone bodies beta-hydroxybutyrate or acetoacetate) reduced the spontaneous firing rate of neurons in slices from rat or mouse substantia nigra pars reticulata. This region is thought to act as a seizure gate, controlling seizure generalization. Consistent with an anticonvulsant role, the ketone body effect is larger for cells that fire more rapidly. The effect of ketone bodies was abolished by eliminating the metabolically sensitive K(ATP) channels pharmacologically or by gene knock-out. We propose that ketone bodies or glycolytic restriction treat epilepsy by augmenting a natural activity-limiting function served by KATP channels in neurons.

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