首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >Aggregation of amyloid beta-protein as function of age and apolipoprotein E in normal and Alzheimer's serum.
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Aggregation of amyloid beta-protein as function of age and apolipoprotein E in normal and Alzheimer's serum.

机译:正常人和阿尔茨海默氏病患者血清中淀粉样β蛋白的聚集与年龄和载脂蛋白E的关系。

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We compared the effect of serum from (a) 26 Alzheimer's disease (AD) patients and 22 age-matched non-demented controls (CO) with apolipoprotein E 4/4, 3/3 or 3/2 phenotypes, and (b) 17 normal young (aged 15-41 years) and 21 normal elderly (aged 64-83 years) people on in vitro aggregation of synthetic amyloid beta-protein (A beta) 1-40 by Thioflavin T fluorescence spectroscopy. A beta 1-40 aggregation in presence of serum from the normal elderly group was significantly higher as compared to the normal young group (correlation coefficient between age and A beta aggregation=0.73). However, no difference in A beta aggregation was observed in the presence of serum from AD patients and non-demented controls. There was a positive correlation between serum apo E concentrations and A beta aggregation, while there was no significant difference between different apo E phenotypes. The correlation coefficient in the AD 4/4 (0.65) was higher than the CO 4/4 group (0.04), while it was lower in the AD 3/3 group (-0.12) than in the CO 3/3 (0.39) group. These results suggest that the apo E4 allele alone may not be responsible for A beta fibril formation in AD; other factors may be involved in increasing risk for AD pathogenesis in those having the apo E4 allele. The severity of dementia and serum albumin levels also did not correlate with A beta aggregation. We propose that the age of an individual may be an important factor in determining the degree of A beta aggregation/fibrillization, and that mechanism of sequestration of A beta in serum may not be defective in AD.
机译:我们比较了载脂蛋白E 4 / 4、3 / 3或3/2表型与(a)26位阿尔茨海默氏病(AD)患者和22位年龄匹配的非痴呆对照(CO)血清的影响,以及(b)17硫黄素T荧光光谱法在体外聚集1-40的合成淀粉样β蛋白(A beta)的正常年轻人(15-41岁)和21位正常老人(64-83岁)中。与正常年轻人组相比,正常老年人组中存在血清的β1-40聚集显着更高(年龄与Aβ聚集之间的相关系数为0.73)。然而,在来自AD患者和非痴呆对照的血清中,未观察到Aβ聚集的差异。血清载脂蛋白E浓度与Aβ聚集之间呈正相关,而不同载脂蛋白E表型之间无显着差异。 AD 4/4(0.65)的相关系数高于CO 4/4组(0.04),而AD 3/3组(-0.12)的相关系数低于CO 3/3(0.39)组。这些结果表明,单独的载脂蛋白E4等位基因可能不负责AD中Aβ原纤维的形成。其他具有apo E4等位基因的人可能与增加AD发病机理的风险有关。痴呆的严重程度和血清白蛋白水平也与Aβ聚集无关。我们建议,个体年龄可能是决定Aβ聚集/原纤维化程度的重要因素,并且血清中Aβ隔离的机制可能在AD中没有缺陷。

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