高迁移率组Box-1在癫痫持续状态中的作用,从病理生理学到生物标志物和治疗潜力

Rana M. Raoof, M. Al-Hamdany, Khalida I. Noel
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引用次数: 1

摘要

癫痫持续状态(SE)是一种神经急症,由于其相关的死亡率和发病率,需要及时诊断和治疗措施。神经炎症在癫痫持续状态中的作用已被广泛研究,许多潜在的分子已被提出作为有前途的生物标志物和治疗靶点。在细胞核内,HMGB1是一种具有许多家务功能的dna结合蛋白。在一定条件下,HMGB1会转移到细胞外空间,促进强烈的促炎反应,激活许多与癫痫发作和进展相关的下游炎症途径。这篇综述强调了HMGB1在SE发病机制中的潜在作用,并强调了该分子作为SE治疗靶点的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of High Mobility Group Box-1 in Status Epilepticus, From Pathophysiology to Biomarker and Therapeutic Potential
Status epilepticus (SE) is a neurological emergency that require prompt diagnostic and treatment measures due to its associated mortality and morbidity. The role of neuro-inflammation in status epilepticus has been studied extensively and many potential molecules have been proposed as a promising biomarkers and therapeutic targets for the condition. Inside the nucleus, HMGB1 is a DNA-binding protein with many housekeeping functions. Under certain conditions, HMGB1 will be translocated to the extracellular space promoting a strong pro-inflammatory reaction with activation of many downstream inflammatory pathways related to seizure onset and progression. In this review the potential role of HMGB1 in the pathogenesis of SE was highlighted stressing on the promising implications of this molecule as a therapeutic target for SE.
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