Faculty of Physics and Applied Computer Science, AGH University of Science and Technology, Al. Mickiewicza 30, 30-059 Krakow, Poland.
Anal Bioanal Chem. 2012 Dec;404(10):3071-80. doi: 10.1007/s00216-012-6425-5. Epub 2012 Oct 4.
In the present paper, X-ray fluorescence microscopy was applied to follow the processes occurring in rat hippocampal formation during the post-seizure period. In the study, one of the status epilepticus animal models of epilepsy was used, namely the model of temporal lobe epilepsy with pilocarpine-induced seizures. In order to analyze the dynamics of seizure-induced elemental changes, the samples taken from seizure-experiencing animals 3 h and 1, 4, and 7 days after proconvulsive agent administration were analyzed. The obtained results confirmed the utility of X-ray fluorescence microscopy in the research of mechanisms involved in the pathogenesis and progress of epilepsy. The topographic and quantitative elemental analysis of hippocampal formations from different periods of epileptogenesis showed that excitotoxicity, mossy fibers sprouting, and iron-induced oxidative stress may be the processes responsible for seizure-induced neurodegenerative changes and spontaneous recurrent seizures occurring in the chronic phase of the pilocarpine model. The analysis of correlations between the recorded elemental anomalies and quantitative parameters describing animal behavior in the acute period of pilocarpine-induced status epilepticus showed that the areal densities of selected elements measured in the latent period strongly depend on the progress of the acute phase. Especially important seem to be the observations done for Ca and Zn levels which suggest that the intensity of the pathological processes such as excitotoxicity and mossy fibers sprouting depend on the total time of seizure activity. These results as well as dependencies found between the levels of S, K, and Cu and the intensity of maximal seizures clearly confirm how important it is to control the duration and intensity of seizures in clinical practice.
在本研究中,应用 X 射线荧光显微镜技术来研究癫痫发作后大鼠海马结构中发生的过程。在研究中,使用了一种癫痫动物模型,即匹罗卡品诱导癫痫发作的颞叶癫痫模型。为了分析癫痫发作诱导的元素变化的动力学,分析了经历癫痫发作的动物在致惊厥剂给药后 3 小时以及 1、4 和 7 天采集的样本。获得的结果证实了 X 射线荧光显微镜在癫痫发病机制和进展研究中的应用价值。对不同癫痫发生期海马结构的形貌和定量元素分析表明,兴奋性毒性、苔藓纤维发芽和铁诱导的氧化应激可能是导致癫痫发作诱导的神经退行性变化和匹罗卡品模型慢性期自发复发性癫痫的过程。分析记录的元素异常与描述匹罗卡品诱导的癫痫持续状态急性期动物行为的定量参数之间的相关性表明,在潜伏期测量的选定元素的面积密度强烈依赖于急性期的进展。对于 Ca 和 Zn 水平的观察似乎尤为重要,这些观察结果表明,兴奋性毒性和苔藓纤维发芽等病理过程的强度取决于癫痫发作活动的总时间。这些结果以及在 S、K 和 Cu 水平与最大癫痫发作强度之间发现的依赖性清楚地证实了在临床实践中控制癫痫发作的持续时间和强度是多么重要。