首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Long-term expression of Fos-related antigen and transient expression of delta FosB associated with seizures in the rat hippocampus and striatum.
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Long-term expression of Fos-related antigen and transient expression of delta FosB associated with seizures in the rat hippocampus and striatum.

机译:大鼠海马和纹状体中与癫痫发作相关的Fos相关抗原的长期表达和δFosB的瞬时表达。

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摘要

Systemic administration of kainic acid (KA), an analogue of glutamic acid, causes limbic seizures and pathophysiological changes in adult rats that are very similar to human temporal lobe epilepsy. One of the earliest changes in gene expression after treatment with KA is the induction of immediate-early genes. The fos and jun families are frequently studied immediate-early genes that are induced by KA. Several groups, including ours, have recently reported that a 35-kDa Fos-related antigen (FRA) is induced for a protracted time by various stimuli. It has been suggested that this FRA is delta FosB, which has a molecular mass of approximately 35 kDa. The present study characterizes the long-term expression of FRA and delta FosB after systemic treatment with KA. Immunocytochemistry and western blot analysis using an antibody that cross-reacts with all known FRAs showed that a 35-kDa FRA was induced at high levels in both the hippocampus and striatum for up to 1 month by KA. A semiquantitative PCR analysisshowed that delta FosB was induced by KA, but its expression lasted for only 6 h. This result was also verified by northern blot analysis. These results suggested that the 35-kDa FRA with long-term elevated levels seen with western blot analysis and immunocytochemistry is a new species of the FRA and not delta FosB. The long-term expression of FRA in both the hippocampus and striatum may be associated with the pathophysiological changes after KA administration.
机译:海藻酸(KA)(一种谷氨酸的类似物)的全身给药会导致成年大鼠的边缘性癫痫发作和病理生理变化,这与人类颞叶癫痫非常相似。 KA处理后基因表达的最早变化之一是诱导即早基因。 fos和jun家族经常研究由KA诱导的即早基因。包括我们在内的几个小组最近都报告说,各种刺激会在延长的时间内诱导35 kDa Fos相关抗原(FRA)。已经提出,该FRA是δFosB,其分子量约为35kDa。目前的研究表征了KA全身治疗后FRA和δFosB的长期表达。使用与所有已知FRA交叉反应的抗体进行的免疫细胞化学和蛋白质印迹分析表明,KA可在海马和纹状体中高水平诱导35 kDa FRA长达1个月。半定量PCR分析表明,δFosB是由KA诱导的,但其表达仅持续了6小时。该结果也通过RNA印迹分析证实。这些结果表明,通过蛋白质印迹分析和免疫细胞化学观察到的具有长期升高水平的35 kDa FRA是FRA的新物种,而不是δFosB。 FKA在海马和纹状体中的长期表达可能与KA给药后的病理生理变化有关。

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