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首页> 外文期刊>Annals of neurology >Seizure-induced brain-borne inflammation sustains seizure recurrence and blood-brain barrier damage
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Seizure-induced brain-borne inflammation sustains seizure recurrence and blood-brain barrier damage

机译:癫痫病诱发的脑源性炎症维持癫痫发作复发和血脑屏障损害

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摘要

Objective: Epilepsy is a common neurological disorder characterized by recurrent seizures often unresponsive to pharmacological treatment. Brain inflammation is considered a crucial etiopathogenetic mechanism of epilepsy that could be targeted to control seizures. Specific inflammatory mediators overexpressed in human epileptogenic foci are known to promote seizures in animal models. We investigated whether seizures induce brain inflammation independently on extracerebral factors. We also investigated whether brain-borne inflammation is required and sufficient to maintain seizure activity and whether it causes blood-brain barrier (BBB) impairment. We addressed these questions by studying the relation between seizures, inflammation, and BBB permeability in a brain preparation isolated from extracerebral compartments. Methods: Epileptiform activity was induced by arterial perfusion of bicuculline in the in vitro isolated guinea pig brain. Seizure-induced brain inflammation was evaluated by quantitative immunohistochemical analysis of interleukin (IL)-1β in parenchymal cells. BBB damage was assessed by extravasation of intravascular fluorescein isothiocyanate-albumin. The effects of arterially perfused anakinra, a human recombinant IL-1β receptor antagonist, were investigated on epileptiform discharges, brain inflammation, and BBB damage. Results: Seizure induction in the absence of extracerebral factors promoted the release of IL-1β from brain resident cells and enhanced its biosynthesis in astrocytes. Anakinra rapidly terminated seizures, prevented their recurrence, and resolved seizure-associated BBB breakdown. Interpretation: Seizures initiate brain inflammation in glia and promote BBB damage that is independent of either leukocytes or blood-borne inflammatory molecules. Brain inflammation contributes to the duration and recurrence of seizures. This study supports the use of specific anti-inflammatory drugs in clinical conditions that present with intractable recurrent seizures.
机译:目的:癫痫病是一种常见的神经系统疾病,其特征在于反复发作通常对药物治疗无反应。脑部炎症被认为是癫痫病的关键发病机制,可以控制癫痫发作。已知在人类癫痫病灶中过表达的特定炎症介质在动物模型中会促进癫痫发作。我们调查了癫痫发作是否独立于脑外因素诱发脑炎症。我们还调查了是否需要脑源性炎症并足以维持癫痫发作活动,以及是否引起血脑屏障(BBB)损伤。我们通过研究癫痫发作,炎症和从脑外隔室分离出的大脑制剂中的血脑屏障通透性之间的关系来解决这些问题。方法:在体外离体的豚鼠脑中,通过比库林的动脉灌注诱导癫痫样活性。通过对实质细胞中白介素(IL)-1β的定量免疫组织化学分析,评估了癫痫发作引起的脑部炎症。通过血管内异硫氰酸荧光素-白蛋白的渗出评估BBB损害。研究了人重组IL-1β受体拮抗剂动脉灌注的anakinra对癫痫样放电,脑部炎症和BBB损伤的影响。结果:在没有脑外因子的情况下诱发癫痫发作促进了脑部驻留细胞中IL-1β的释放,并增强了其在星形胶质细胞中的生物合成。 Anakinra迅速终止了癫痫发作,防止了它们的复发,并解决了癫痫发作相关的BBB分解。解释:癫痫发作可引起神经胶质细胞脑炎,并促进BBB损伤,这种损伤与白细胞或血液传播的炎症分子无关。脑部炎症有助于癫痫发作的持续时间和复发。这项研究支持在难治性复发性癫痫发作的临床情况下使用特定的抗炎药。

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