The efficacy of fructose-1,6-bisphosphate in suppressing status epilepticus in developing rats

被引:4
|
作者
Janicot, Remi [1 ]
Stafstrom, Carl E. [1 ]
Shao, Li-Rong [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Div Pediat Neurol, Baltimore, MD 21205 USA
关键词
Metabolism; Glycolysis; Pediatric seizures; Anti-seizure medication (ASM); Developing brain; ANTICONVULSANT; 2-DEOXY-D-GLUCOSE; SEIZURES; EPILEPSY;
D O I
10.1016/j.eplepsyres.2020.106500
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Treatment of pediatric status epilepticus (SE) remains challenging as up to 50 % of patients are refractory to conventional anti-seizure medications. The glycolytic intermediate, fructose-1,6-bisphosphate (FBP), has been reported to exert significant anticonvulsant effects in both adult animals and in in vitro models of seizures. This study aims to examine FBP efficacy in controlling seizures in a rat model of juvenile SE. Methods: Sprague Dawley rats (P11-P17) were injected with pilocarpine (300 mg/kg, i.p.) to induce SE, which was monitored by video-electroencephalography (v-EEG). Thirty minutes into SE, FBP was administrated (500 or 1000 mg/kg, i.p.). v-EEG recording was continued for-60 additional minutes to assess the anticonvulsant effect of FBP, compared with vehicle (saline) treatment. Results: SE consistently occurred in rat pups 10-15 min after pilocarpine injection and persisted over the 90-min recording period. Neither saline nor a lower dose of FBP (500 mg/kg) treatment stopped behavioral and electrographic seizures. At higher doses (1000 mg/kg), FBP terminated SE in-15 min in 60 % (6 of 10) of the rat pups. Conclusion: The endogenous glycolytic metabolite, FBP, promptly suppresses ongoing seizure activity and represents a potential alternative metabolic therapy to improve the treatment of SE in the juvenile age range.
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页数:5
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