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Increase in seizure susceptibility in sepsis like condition explained by spiking cytokines and altered adhesion molecules level with impaired blood brain barrier integrity in experimental model of rats treated with lipopolysaccharides

机译:癫痫发育中癫痫发育敏感性增加,如掺马细胞因子和粘附分子水平随血液多糖对大鼠实验模型的血脑屏障完整性损伤的粘附分子水平解释的病症

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Highlights ? Sepsis like inflammatory states increase the seizure susceptibility. ? Oxidative stress might play role in increased seizures in sepsis. ? Changes in cytokines, adhesive molecules level affect the vulnerability to seizures. ? Challenged blood brain barrier integrity leads to increase in seizures. Abstract Background and objective Epilepsy is a neurological disorder characterized by recurrent unprovoked seizures. Sepsis is a condition which initiates a cascade of a surge of inflammatory mediators. Interplay between seizures and inflammation other than of brain origin is yet to be explored. The present study was designed to evaluate the seizure susceptibility in experimental models of lipopolysaccharide (LPS) induced sepsis. Design and methods Experimental sepsis was induced using lipopolysaccharides in Wistar rats. Valproic acid, dexametasone were given to two different groups of animals along with LPS. Two groups of animals were subjected to administration of vehicle and LPS respectively with no other treatment. 24 h later, animals were subjected to seizures by using either maximal electro shock or pentylenetetrazole. Seizures related parameters, oxidative stress and TNF-α, IL-6, IL-1β, ICAM-1, ICAM-2, VCAM-1, MMP-9 level in serum and brain samples were evaluated. Histopathological and blood brain barrier permeability studies were conducted. Results Seizures were decreased in valproic acid treated animals. Reduced oxidative stress was seen in dexamethasone plus valproic acid treated groups as compared to LPS alone treated group. TNF-α, IL-6, IL-1β, ICAM-1, VCAM-1, MMP-9 levels were found increased in LPS treated animals whereas a reverse observation was noted for ICAM-2 level in brain and serum. Histopathological findings confirmed the successful establishment of sepsis like state in animals. Blood brain barrier permeability was found increased in LPS treated groups of animals. Conclusion Seizure susceptibility may escalate during the sepsis like inflammatory conditions and curbing the inflammatory state might reverse the phenomenon.
机译:强调 ?脓毒症如炎症状态增加癫痫发作敏感性。还氧化应激可能在败血症中癫痫发作增加中发挥作用。还细胞因子的变化,粘合剂分子水平影响癫痫发作的脆弱性。还挑战性血脑屏障完整性导致癫痫发作增加。摘要背景和目的癫痫是一种神经系统疾病,其特征在于经常性未加工的癫痫发作。败血症是一种发起炎症介质血液循序物的条件。癫痫发作和炎症之间的相互作用尚未探索脑来源以外的癫痫发作。本研究旨在评估脂多糖(LPS)诱导的败血症实验模型中的癫痫发作敏感性。使用Wistar大鼠脂多糖诱导设计和方法实验败血症。将甲己酸,瓦络酸甲酸,与LPS一起给两组不同的动物。对两组动物进行载体和LPS,没有其他处理。 24小时后,通过使用最大电休克或五苯乙烯释放唑来进行动物癫痫发作。评价癫痫发作相关参数,氧化应激和TNF-α,IL-6,IL-1β,ICAM-1,ICAM-2,VCAM-1,血清和脑样品中的MMP-9水平。进行组织病理学和血脑屏障渗透性研究。丙戊酸处理的动物中癫痫发作减少。与单独的LPS单独处理的基团相比,在地塞米松加丙甲酸处理基团中看到降低氧化应激。在LPS处理的动物中发现TNF-α,IL-6,IL-1β,ICAM-1,VCAM-1,MMP-9水平,而ICAM-2水平在脑和血清中均有逆向观察。组织病理学发现证实了在动物中成功建立了脓毒症。在LPS处理的动物组中发现血脑屏障渗透性增加。结论癫痫发育敏感性可能在脓毒症等炎症条件如炎症条件下升高,抑制炎症状态可能会扭转现象。

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