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2DG and glycolysis as therapeutic targets for status epilepticus.
Sutula, Thomas P; Fountain, Nathan B.
Afiliação
  • Sutula TP; Department of Neurology, University of Wisconsin, Madison, WI, USA; Hexokine Therapeutics, Inc., Madison, WI, USA. Electronic address: sutula@neurology.wisc.edu.
  • Fountain NB; Department of Neurology, F.E. Dreifuss Comprehensive Epilepsy Program, University of Virginia, Charlottesville, VA, USA; Hexokine Therapeutics, Inc., Madison, WI, USA.
Epilepsy Behav ; 140: 109108, 2023 03.
Article em En | MEDLINE | ID: mdl-36804714
2-deoxy-D-glucose (2DG) is a glucose analog differing from glucose only by removal of an oxygen atom at the 2 position, which prevents the isomerization of glucose-6-phosphate to fructose-6-phosphate, and thereby reversibly inhibits glycolysis. PET studies of regional brain glucose utilization positron-emitting 18F-2DG demonstrate that brain regions generating seizures have diminished glucose utilization during interictal conditions, but rapidly transition to markedly increased glucose delivery and utilization during seizures, particularly in status epilepticus (SE). 2-deoxy-D-glucose has acute antiseizure actions in multiple in vivo and in vitro seizure models, including models of SE induced by the chemo convulsants pilocarpine and kainic acid, suggesting that focal enhanced delivery of 2DG to ictal brain circuits is a potential novel anticonvulsant intervention for the treatment of SE.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Desoxiglucose Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estado Epiléptico / Desoxiglucose Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article