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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Higher expression of monocyte chemoattractant protein 1 and its receptor in brain tissue of intractable epilepsy patients
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Higher expression of monocyte chemoattractant protein 1 and its receptor in brain tissue of intractable epilepsy patients

机译:顽固性癫痫患者脑组织中单核细胞化学抑制剂蛋白1及其受体的更高表达

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We aimed to explore the pathogenesis of monocyte chemoattractant protein-1 (MCP1) and CC chemokine receptor 2 (CCR2) in brain tissue of patients with intractable epilepsy (IE). Hippocampi or temporal lobe tissues were obtained from 40 patients with IE and five patients without IE who had undergone surgical decompression and debridement. The levels of MCP1 and CCR2 were evaluated using immunohistochemistry. Pearson correlation analysis was employed to evaluate the correlation between levels of MCP1 and CCR2 in IE with or without hippocampal sclerosis (HS) and the disease duration, along with age. Higher levels of MCP1 (11.68 +/- 4.68% versus 1.72 +/- 1.54%) and CCR2 (11.54 +/- 4.65% versus 1.52 +/- 1.29%; P < 0.05) were observed in IE patients compared to controls. Expression levels of MCP1 (R = 0.867) and CCR2 (R = 0.835) in IE patients with HS were correlated with the disease duration. However, no correlation was found in IE patients without HS. There was also no correlation between levels of MCP1 and CCR2 in IE patients with age, either with HS or without HS. These results suggest that MCP1 and its receptor may play a role in the pathogenesis and progression of IE. (C) 2015 Elsevier Ltd. All rights reserved.
机译:我们的旨在探讨单核细胞化学蛋白-1(MCP1)和CC趋化因子受体2(CCR2)的脑组织患者的脑组织(IE)的脑组织发病机制。从40例IE和5名患者获得HIPPOCAMPI或颞叶组织,没有IE没有IE的患者进行手术减压和清新。使用免疫组织化学评估MCP1和CCR2的水平。 Pearson相关分析用于评估MCP1和CCR2水平之间的相关性,IE有或没有海马硬化症(HS)和疾病持续时间。在IE患者中,在IE患者中,在IE患者与对照组中,观察到更高水平的MCP1(11.68 +/- 1.54%)和CCR2(11.54 +/- 1.54%; P <0.05)。 MCP1(r = 0.867)和CCR2(R = 0.835)的表达水平在HS患者中与疾病持续时间相关。然而,在没有HS的患者中没有发现任何相关性。 MCP1和CCR2在IE患者中的患者之间也没有相关性,无论是HS还是没有HS。这些结果表明MCP1及其受体可能在发病机制和IE的进展中发挥作用。 (c)2015 Elsevier Ltd.保留所有权利。

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