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首页> 外文期刊>Neurology India >Association of Genetic Polymorphisms in Tumor Necrosis Factor-Alpha gene with the risk of Intracerebral Hemorrhage in North Indian Population
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Association of Genetic Polymorphisms in Tumor Necrosis Factor-Alpha gene with the risk of Intracerebral Hemorrhage in North Indian Population

机译:肿瘤坏死因子-α基因遗传多态性与北印度人口脑出血风险的关系

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摘要

Intracerebral Hemorrhage (ICH) refers to the bleeding in the intracranial vault, meninges, and also the brainparenchyma.[1] Microglia are the inhabiting immune cells in the brain. An injury to the brain results in theactivation of these microglial cells. Various states of modulation of microglia can have either neurotoxic orneuroprotective effect. An inflammatory molecule tumor necrosis factor-alpha (TNF-alpha) derived fromactivated microglia has not only been shown to induce the production of other inflammatory molecules butalso as an autocrine mediator in microglial activation in response to traumatic brain injury (TBI) and spinalcord injury (SCI).[2],[3] Alteration in the TNF-alpha expression has been associated with cerebral aneurysmsand subarachnoid hemorrhage but no direct role has been established.[4],[5] There are limited reports oninvestigation of the association between TNF-α gene polymorphism and the risk of hemorrhagic stroke inmultiple ethnicities. Ruigrok et al. have evaluated the role of APOE, IGF-1, TNF-alpha among other genes insubarachnoid hemorrhage, which has established the role of TNF-alpha as a high risk factor.[6] The pathwayby which TNF-alpha cause ICH is yet to be identified.
机译:脑内出血(ICH)是指颅内拱顶,脑膜和脑膜癌的出血。[1]小胶鸡是大脑中的居住的免疫细胞。对大脑的伤害导致这些微胶质细胞的灭活。微胶质细胞调节的各种调节可以具有神经毒性血管保护作用。衍生的炎症分子肿瘤坏死因子-α(TNF-α)衍生的源激活的小胶质细胞源不仅显示出诱导其他炎症分子丁卓在微胶质激活中作为自分泌介质的产生,以应对创伤性脑损伤(TBI)和Spinalcord损伤( SCI)。[2],[3] TNF-α表达的改变已经与脑动脉瘤性血管瘤出血有关,但没有建立直接作用。[4],[5]在TNF之间的关联有限的报告-α基因多态性和出血性中风的风险。 Ruigrok等人。已经评估了Apoe,IGF-1,TNF-α在其他基因中的作用,其在其他基因内的出血,这使得TNF-α的作用是高危因素的作用。[6] TNF-alpha原因ICH的途径尚未识别。

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