首页> 外文期刊>Journal of Alzheimer's disease: JAD >Quantitative Measurement of [Na plus ] and [K plus ] in Postmortem Human Brain Tissue Indicates Disturbances in Subjects with Alzheimer's Disease and Dementia with Lewy Bodies
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Quantitative Measurement of [Na plus ] and [K plus ] in Postmortem Human Brain Tissue Indicates Disturbances in Subjects with Alzheimer's Disease and Dementia with Lewy Bodies

机译:死后人脑组织中[Na +]和[K plus]的定量测量表明患有阿尔茨海默氏病和路易体痴呆的受试者存在干扰

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Alzheimer's disease (AD) is associated with significant disturbances in the homeostasis of Na+ and K+ ions as well as reduced levels of Na+/K+ ATPase in the brain. This study used ICP-MS to accurately quantify Na+ and K+ concentrations in human postmortem brain tissue. We analyzed parietal cortex (Brodmann area 7) from 28 cognitively normal age-matched controls, 15 cases of moderate AD, 30 severe AD, and 15 dementia with Lewy bodies (DLB). Associations were investigated between [Na+] and [K+] and a number of variables including diagnosis, age, gender, Braak tangle stage, amyloid-beta (A beta) plaque load, tau load, frontal tissue pH, and APOE genotype. Brains from patients with severe AD had significantly higher (26%; p < 0.001) [Na+] (mean 65.43 +/- standard error 2.91 mmol/kg) than controls, but the concentration was not significantly altered in moderate AD or DLB. [Na+] correlated positively with Braak stage (r = 0.45; p < 0.0001), indicating association with disease severity. [K+] in tissue was 10% lower (p < 0.05) in moderate AD than controls. However, [K+] in severe AD and DLB (40.97 +/- 1.31 mmol/kg) was not significantly different from controls. There was a significant positive correlation between [K+] and A beta plaque load (r = 0.46; p = 0.035), and frontal tissue pH (r = 0.35; p = 0.008). [Na+] was not associated with [K+] across the groups, and neither ion was associated with tau load or APOE genotype. We have demonstrated disturbances of both [Na+] and [K+] in relation to the severity of AD and markers of AD pathology, although it is possible that these relate to late-stage secondary manifestations of the disease pathology.
机译:阿尔茨海默氏病(AD)与Na +和K +离子体内平衡的显着紊乱以及脑中Na + / K + ATPase水平降低有关。这项研究使用ICP-MS准确定量了人类死后脑组织中的Na +和K +浓度。我们分析了来自28个年龄正常的认知正常对照,15例中度AD,30例重度AD和15例路易体(DLB)痴呆患者的顶叶皮层(Brodmann区域7)。研究了[Na +]和[K +]与许多变量之间的关联,包括诊断,年龄,性别,Braak缠结阶段,淀粉样β(A beta)斑块负荷,tau负荷,额叶组织pH和APOE基因型。患有严重AD的患者的大脑比对照组明显更高(26%; p <0.001)[Na +](平均65.43 +/-标准误差2.91 mmol / kg),但是在中度AD或DLB中,浓度没有明显改变。 [Na +]与Braak分期呈正相关(r = 0.45; p <0.0001),表明与疾病严重程度相关。中度AD患者的组织中[K +]比对照组低10%(p <0.05)。然而,重度AD和DLB(40.97 +/- 1.31 mmol / kg)中的[K +]与对照组无显着差异。 [K +]与Aβ斑块负荷(r = 0.46; p = 0.035)与额叶组织pH值(r = 0.35; p = 0.008)之间存在显着正相关。各组中[Na +]与[K +]不相关,并且两个离子均与tau负荷或APOE基因型无关。我们已经证明了[Na +]和[K +]都与AD的严重程度和AD病理学标记有关,尽管这些疾病可能与疾病病理学的晚期继发表现有关。

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