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首页> 外文期刊>Epilepsy research >The protective effect of a ketogenic diet on kainic acid-induced hippocampal cell death in the male ICR mice.
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The protective effect of a ketogenic diet on kainic acid-induced hippocampal cell death in the male ICR mice.

机译:生酮饮食对海藻酸诱导的雄性ICR小鼠海马细胞死亡的保护作用。

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摘要

This study was designed to evaluate the antiapoptotic effects of a ketogenic diet (KD) through histological (cresyl violet staining, TUNEL staining and immunohistochemistry) and behavioral studies using kainic acid (KA, 25mg/kg i.p.)-induced seizures in male ICR mice. KA-induced seizure in rodents is widely used as an experimental model for human temporal lobe epilepsy because of their behavioral and pathological similarities. A KA-induced seizure causes neuronal damage in hippocampal pyramidal neurons and involves a caspase-3-mediated apoptotic pathway. In this study, the seizure onset time of the KD-fed group was delayed compared to that of the group fed a normal diet (ND) after a systemic KA injection. Histological studies revealed that KA caused pyknosis in most of the hippocampal areas in the ND-fed group, however, well-preserved pyramidal neurons were detected in the hippocampus of mice that had been on KD for 1 month, which began on postnatal day 21. The number of TUNEL-positive cells and caspase-3-positive cells in the hippocampus of the KD-fed group was lower than that of the ND-fed group. These findings indicate that KD has an antiepileptic effect via a neuroprotective action that involves the inhibition of caspase-3-mediated apoptosis of hippocampal neurons.
机译:这项研究旨在通过组织学(甲苯酚紫染色,TUNEL染色和免疫组化)和使用海藻酸(KA,25mg / kg腹膜内注射)诱导的雄性ICR小鼠癫痫发作的行为学研究,评估生酮饮食(KD)的抗凋亡作用。 KA诱导的啮齿动物癫痫发作因其行为和病理相似性而被广泛用作人类颞叶癫痫的实验模型。 KA诱发的癫痫发作会引起海马锥体神经元的神经元损伤,并涉及caspase-3介导的凋亡途径。在这项研究中,与全身性KA注射后正常饮食(ND)组相比,KD喂养组的癫痫发作时间被延迟。组织学研究表明,在ND喂养组中,KA导致大部分海马区发生缩,但是,在出生后第21天开始接受KD治疗1个月的小鼠海马中检测到保存完好的锥体神经元。 KD喂养组海马的TUNEL阳性细胞和caspase-3阳性细胞的数量低于ND喂养组。这些发现表明,KD通过神经保护作用具有抗癫痫作用,其中涉及抑制caspase-3介导的海马神经元凋亡。

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