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阿尔茨海默病患者的必需和非必需金属的脑脊液/血浆比率。

Cerebrospinal fluid/plasma quotients of essential and non-essential metals in patients with Alzheimer's disease.

机构信息

Department of Occupational and Environmental Medicine, Sahlgrenska Academy and University Hospital, Box 414, SE-40530 Gothenburg, Sweden.

出版信息

J Neural Transm (Vienna). 2011 Jun;118(6):957-62. doi: 10.1007/s00702-011-0605-x. Epub 2011 Mar 4.

Abstract

In this study, the quotients (Q) between metal concentrations in cerebrospinal fluid (CSF) and plasma were studied in subjects with Alzheimer's disease (AD) and referents to investigate if the leakage through the blood-CSF barrier (BCB) increased with increased duration and severity of the disease. Concentrations of 18 metals (Mg, Ca, Mn, Fe, Co, Ni, Cu, Zn, Se, Rb, Sr, Mo, Cd, Sn, Sb, Cs, Hg, and Pb) were determined by ICP-MS in plasma and cerebrospinal fluid in 264 patients with AD, and in 54 healthy referents. The quotients Q (Mn), Q (Rb), Q (Sb), Q (Pb) and Q (Hg) were significantly lower (p ≤ 0.003) and Q (Co) significantly higher (p ≤ 0.001) in subjects with AD as compared with the controls. Subjects in a subgroup with more severe AD, showed the same pattern. The metal leakage into CSF did not increase with increased duration and/or severity of the disease. The permeability of BCB varied considerably between the studied metals with low median quotients (Q ≤ 0.02) for Cd, Cu, Sb, Se and Zn and higher median quotients for Ca (Q ~ 0.5) and Mg (Q ~ 1.3), probably partly depending on differences in size and lipophilicity of metal-carrier complexes and specific carrier mechanisms.

摘要

在这项研究中,研究了阿尔茨海默病(AD)患者和对照者脑脊液(CSF)和血浆中金属浓度的商(Q),以调查随着疾病持续时间和严重程度的增加,血脑屏障(BCB)的渗漏是否增加。通过 ICP-MS 测定了 264 名 AD 患者和 54 名健康对照者血浆和脑脊液中 18 种金属(Mg、Ca、Mn、Fe、Co、Ni、Cu、Zn、Se、Rb、Sr、Mo、Cd、Sn、Sb、Cs、Hg 和 Pb)的浓度。与对照组相比,AD 患者的 Q(Mn)、Q(Rb)、Q(Sb)、Q(Pb)和 Q(Hg)明显较低(p≤0.003),Q(Co)明显较高(p≤0.001)。在 AD 亚组中病情较重的患者中,也出现了同样的模式。金属向 CSF 的渗漏并未随疾病持续时间和/或严重程度的增加而增加。BCB 的通透性在研究的金属之间差异很大,低中位数商(Q≤0.02)适用于 Cd、Cu、Sb、Se 和 Zn,而 Ca(Q0.5)和 Mg(Q1.3)的中位数商较高,这可能部分取决于金属载体复合物的大小和疏水性以及特定的载体机制的差异。

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