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Repeated febrile convulsions impair hippocampal neurons and cause synaptic damage in immature rats: neuroprotective effect of fructose-1,6-diphosphate

机译:反复发热抽搐损害海马神经元并导致未成熟大鼠突触损伤:果糖-1,6-二磷酸的神经保护作用

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Fructose-1,6-diphosphate is a metabolic intermediate that promotes cell metabolism. We hypothesize that fructose-1,6-diphosphate can protect against neuronal damage induced by febrile convulsions. Hot-water bathing was used to establish a repetitive febrile convulsion model in rats aged 21 days, equivalent to 3-5 years in humans. Ninety minutes before each seizure induction, rats received an intraperitoneal injection of low- or high-dose fructose-1,6-diphosphate (500 or 1,000 mg/kg, respectively). Low- and high-dose fructose-1,6-diphosphate prolonged the latency and shortened the duration of seizures. Furthermore, high-dose fructose-1,6-diphosphate effectively reduced seizure severity. Transmission electron microscopy revealed that 24 hours after the last seizure, high-dose fructose-1,6-diphosphate reduced mitochondrial swelling, rough endoplasmic reticulum degranulation, Golgi dilation and synaptic cleft size, and increased synaptic active zone length, postsynaptic density thickness, and synaptic interface curvature in the hippocampal CA1 area. The present findings suggest that fructose-1,6-diphosphate is a neuroprotectant against hippocampal neuron and synapse damage induced by repeated febrile convulsion in immature rats.
机译:果糖-1,6-二磷酸是一种代谢中间体,可促进细胞代谢。我们假设果糖-1,6-二磷酸可以保护通过发热抽搐诱导的神经元损伤。热水沐浴用于在21天老鼠的大鼠中建立重复的发热痉挛模型,相当于人类3-5岁。每次癫痫发作前9分钟,大鼠接受腹膜内注射低剂量的低剂量果糖-1,6-二磷酸(500或1,000mg / kg)。低剂量的果糖-1,6-二磷酸延长延迟并缩短了癫痫发作的持续时间。此外,高剂量的果糖-1,6-二磷酸有效减少了癫痫发作严重程度。透射电子显微镜显示,最后一次癫痫发作后24小时,高剂量果糖-1,6-二磷酸,减少线粒体肿胀,粗糙的内质网脱粒,较高的突触有源区长度,突触突破性密度厚度,和海马CA1区域中的突触界面曲率。本研究结果表明,果糖-1,6-二磷酸盐是对海马神经元的神经保护剂,并在未成熟的大鼠中反复发热痉挛引起的突触损伤。

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