Abstract

The ketogenic diet is used as a diet treatment for drug-resistant epilepsy, but there are no antiepileptic drugs based on the ketogenic diet. The ketogenic diet changes energy metabolites (ketone bodies, glucose and lactate) in the brain, which consequently changes electrical activities in neurons and ultimately suppresses seizures in epileptic patients. In order to elucidate the antiseizure effects of the ketogenic diet, it is important to clarify the mechanism by which these metabolic changes are converted to electrical changes in neurons. In this review, we summarize electrophysiological studies focusing on electrical control in neurons by the ketogenic diet. Recent studies have identified electrical regulators driven by the ketogenic diet: ion channels (ATP-sensitive K+ channels and voltage-dependent Ca2+ channels), synaptic receptors (AMPA-type glutamate receptors and adenosine A1 receptors), neurotransmitter transporters (vesicular glutamate transporters), and others (BCL-2-associated agonist of cell death and lactate dehydrogenase). Thus, the ketogenic diet presumably elicits neuronal inhibition via the combined actions of these molecules. From the viewpoint of drug development, these molecules are valuable as targets for the development of new antiepileptic drugs. Drug therapy to mimic the ketogenic diet may be feasible in the future, through the combination of multiple antiepileptic drugs targeting these molecules.

Highlights

  • Electrical Control in Neurons by the Ketogenic DietControl in Neurons by the Ketogenic Diet

  • Neurons, which are connected by synapses, exhibit electrical activities in the living brain

  • Since seizures are elicited by the hyperexcitation of electrical activities in neurons, it is mechanistically presumed that the ketogenic diet acts on the molecules generating electrical currents, such as ion channels and synaptic receptors

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Summary

Electrical Control in Neurons by the Ketogenic Diet

Control in Neurons by the Ketogenic Diet. The ketogenic diet changes energy metabolites (ketone bodies, glucose and lactate) in the brain, which changes electrical activities in neurons and suppresses seizures in epileptic patients. We summarize electrophysiological studies focusing on electrical control in neurons by the ketogenic diet. Recent studies have identified electrical regulators driven by the ketogenic diet: ion channels (ATP-sensitive K+ channels and voltage-dependent Ca2+ channels), synaptic receptors (AMPA-type glutamate receptors and adenosine A1 receptors), neurotransmitter transporters (vesicular glutamate transporters), and others (BCL-2associated agonist of cell death and lactate dehydrogenase). The ketogenic diet presumably elicits neuronal inhibition via the combined actions of these molecules. Drug therapy to mimic the ketogenic diet may be feasible in the future, through the combination of multiple antiepileptic drugs targeting these molecules

INTRODUCTION
MOLECULES FOR ELECTRICAL CONTROL BY THE KETOGENIC DIET
Vesicular Glutamate Transporters
Lactate Dehydrogenase
DRUG DEVELOPMENT BASED ON THE KETOGENIC DIET
Findings
CONCLUSION
Full Text
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