The Antiepileptic Effect of the Glycolytic Inhibitor 2-Deoxy-d-Glucose is Mediated by Upregulation of KATP Channel Subunits Kir6.1 and Kir6.2

H Yang, R Guo, J Wu, Y Peng, D Xie, W Zheng… - Neurochemical …, 2013 - Springer
H Yang, R Guo, J Wu, Y Peng, D Xie, W Zheng, X Huang, D Liu, W Liu, L Huang, Z Song
Neurochemical research, 2013Springer
Metabolic modulation of neuronal excitability is becoming increasingly important as an
antiepileptic therapy. It was reported that the glycolytic inhibitor 2-deoxy-d-glucose (2-DG)
and the activation of the ATP-sensitive potassium ion channel (K ATP channel) had an
antiepileptic effect in models of epilepsy. To explore whether 2-DG exerts an antiepileptic
effect through upregulation of the K ATP channel subunits Kir6. 1 and Kir6. 2, the expression
of these subunits in hippocampus of five groups of mice with pilocarpine-induced status …
Abstract
Metabolic modulation of neuronal excitability is becoming increasingly important as an antiepileptic therapy. It was reported that the glycolytic inhibitor 2-deoxy-d-glucose (2-DG) and the activation of the ATP-sensitive potassium ion channel (KATP channel) had an antiepileptic effect in models of epilepsy. To explore whether 2-DG exerts an antiepileptic effect through upregulation of the KATP channel subunits Kir6.1 and Kir6.2, the expression of these subunits in hippocampus of five groups of mice with pilocarpine-induced status epilepticus (SE) was evaluated. A seizure group with pilocarpine-kindling convulsions (EP) was compared to similar groups treated with high, medium, and low 2-DG concentrations (100–500 mg/kg) and a normal control group (Con). Kir6.1 and Kir6.2 mRNAs and proteins were analyzed at 4 h, 1 days (acute period), 7 days (latent period), 30, and 60 days (chronic period) following SE. In the seizure group (compared to the Con group), hippocampal expression of Kir6.1 and Kir6.2 increased dramatically at 1, 7, and 30 days, and was further increased after treatment with medium and high dose 2-DG (all P < 0.05). Our results suggest that 2-DG may exert an antiepileptic effect through up-regulation of mRNAs and protein levels of Kir6.1 and Kir6.2, which may therefore be used as molecular targets in the treatment of epilepsy with 2-DG.
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