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首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Platelet activating factor is elevated in cerebral spinal fluid and plasma of patients with relapsing-remitting multiple sclerosis.
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Platelet activating factor is elevated in cerebral spinal fluid and plasma of patients with relapsing-remitting multiple sclerosis.

机译:复发缓解型多发性硬化症患者的脑脊液和血浆中的血小板活化因子升高。

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摘要

Platelet-activating factor (PAF) is a phospholipid mediator of inflammation with a wide range of biological activities, including the alteration of barrier function of endothelium. A biological assay combined with high pressure liquid chromatography-tandem mass spectrometry showed that plasma and cerebral spinal fluid (CSF) PAF levels in 20 patients with relapsing/remitting or secondary progressive multiple sclerosis (MS) studied by magnetic resonance imaging (MRI) were significantly higher than in healthy controls (plasma: 3.29+/-4.52 vs. 0.48+/-0.36 ng/ml, p < 0.002; CSF: 4.95+/-6.22 ng/ml vs. 0.01+/-0.04 ng/ml, p < 0.0001). Values were also significantly higher in relapsing/remitting than in secondary progressive (plasma: 5.10+/-4.97 vs. 0.52+/-0.85 ng/ml, p < 0.005; CSF: 8.59+/-6.39 vs. 0.55+/-0.68 ng/ml, p < 0.002). It was also found that both plasma (R2: 0.65) and CSF (R2:0.72) levels were correlated with the MRI number of gadolinium enhancing lesions, which are markers of blood-brain barrier (BBB) injury, whereas their peaks were not correlated with the MRI number of white matter lesions, nor with the expanded disability status score (EDSS) according to Kurtze [Kurtze, J.F., 1983. Rating neurological impairment in multiple sclerosis: an expanded disability scale (EDSS). Neurology 33, 1444-1452]. Both plasma and CSF in patients with relapsing/remitting MS and marked gadolinium enhancement contained the two major molecular species of PAF: 1-0-hexadecyl- (C16:O) and 1-0-octadecyl-sn-glycero-3-phosphocholine (C18:O). The ratio of the two molecular species was different in the two biological fluids, being PAF C18:0 more abundant in CSF and PAF C16:0 in plasma, indicating a different cellular origin of PAF or different enzymatic processing. These findings suggest that PAF is a significant mediator of BBB injury in the early stages of MS, rather than a marker of its progression and severity.
机译:血小板活化因子(PAF)是炎症的磷脂介质,具有多种生物学活性,包括内皮屏障功能的改变。生物测定结合高压液相色谱-串联质谱分析显示,通过磁共振成像(MRI)研究的20例复发/继发或继发进行性多发性硬化症(MS)患者血浆和脑脊髓液(CSF)PAF水平显着高于健康对照组(血浆:3.29 +/- 4.52 vs. 0.48 +/- 0.36 ng / ml,p <0.002; CSF:4.95 +/- 6.22 ng / ml vs. 0.01 +/- 0.04 ng / ml,p <0.0001)。复发/缓解中的值也显着高于继发进行性患者(血浆:5.10 +/- 4.97 vs. 0.52 +/- 0.85 ng / ml,p <0.005; CSF:8.59 +/- 6.39 vs. 0.55 +/- 0.68 ng / ml,p <0.002)。还发现血浆(R2:0.65)和CSF(R2:0.72)的水平均与enhancing增强病变的MRI数量相关,which增强病变是血脑屏障(BBB)损伤的标志物,而其峰值却不相关根据Kurtze [Kurtze,JF,1983。]用白质病灶的MRI数目,也没有使用扩展的残疾状态评分(EDSS)。评估多发性硬化症的神经系统损害:扩展的残疾量表(EDSS)。神经病学,144:1442-1452]。复发/缓解型MS和g明显增强的患者的血浆和CSF都包含PAF的两个主要分子种类:1-0-十六烷基-(C16:O)和1-0-十八烷基-sn-甘油-3-磷酸胆碱( C18:O)。两种生物液体中两种分子的比率不同,CSF中的PAF C18:0含量更高,血浆中的PAF C16:0含量更高,这表明PAF的细胞起源不同或酶处理不同。这些发现表明,PAF是MS早期BBB损伤的重要介体,而不是其进展和严重程度的标志。

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