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S100B raises the alert in subarachnoid hemorrhage

机译:S100B提高蛛网膜下腔出血的警报

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Subarachnoid hemorrhage (SAH) is a devastating disease with high mortality and mobility, the novel therapeutic strategies of which are essentially required. The calcium binding protein S100B has emerged as a brain injury biomarker that is implicated in pathogenic process of SAH. S100B is mainly expressed in astrocytes of the central nervous system and functions through initiating intracellular signaling or via interacting with cell surface receptor, such as the receptor of advanced glycation end products. The biological roles of S100B in neurons have been closely associated with its concentrations, resulting in either neuroprotection or neurotoxicity. The levels of S100B in the blood have been suggested as a biomarker to predict the progress or the prognosis of SAH. The role of S100B in the development of cerebral vasospasm and brain damage may result from the induction of oxidative stress and neuroinflammation after SAH. To get further insight into mechanisms underlying the role of S100B in SAH based on this review might help us to find novel therapeutic targets for SAH.
机译:蛛网膜下腔出血(SAH)是一种具有高死亡率和机动性的毁灭性疾病,其新颖的治疗策略必不可少。钙结合蛋白S100B已经成为一种脑损伤生物标志物,与SAH的致病过程有关。 S100B主要在中枢神经系统的星形胶质细胞中表达,并通过启动细胞内信号传导或通过与细胞表面受体(例如晚期糖基化终产物的受体)相互作用而发挥功能。 S100B在神经元中的生物学作用与其浓度密切相关,从而导致神经保护或神经毒性。血液中S100B的水平已被建议作为预测SAH进展或预后的生物标志物。 S100B在脑血管痉挛发展和脑损伤中的作用可能是由SAH引起的氧化应激和神经炎症引起的。基于此综述,进一步了解S100B在SAH中的作用机理可能有助于我们找到SAH的新型治疗靶标。

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