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本文引用的文献

1
Pathophysiology of white matter perfusion in Alzheimer's disease and vascular dementia.阿尔茨海默病和血管性痴呆的脑白质灌注的病理生理学。
Brain. 2014 May;137(Pt 5):1524-32. doi: 10.1093/brain/awu040. Epub 2014 Mar 10.
2
Assessing white matter ischemic damage in dementia patients by measurement of myelin proteins.评估痴呆症患者的脑白质缺血性损伤:髓鞘蛋白测量法。
J Cereb Blood Flow Metab. 2013 Jul;33(7):1050-7. doi: 10.1038/jcbfm.2013.46. Epub 2013 Mar 27.
3
Convection-enhanced delivery of neprilysin: a novel amyloid-β-degrading therapeutic strategy.血管内递送达普利赛肽:一种新型的淀粉样β降解治疗策略。
J Alzheimers Dis. 2012;32(1):43-56. doi: 10.3233/JAD-2012-120658.
4
Endothelin-1 is elevated in Alzheimer's disease and upregulated by amyloid-β.内皮素-1 在阿尔茨海默病中升高,并被淀粉样β上调。
J Alzheimers Dis. 2012;29(4):853-61. doi: 10.3233/JAD-2012-111760.
5
ACE variants and association with brain Aβ levels in Alzheimer's disease.ACE 变体与阿尔茨海默病大脑 Aβ 水平的关联。
Am J Transl Res. 2010 Oct 15;3(1):73-80.
6
Association cortex hypoperfusion in mild dementia with Lewy bodies: a potential indicator of cholinergic dysfunction?轻度路易体痴呆患者的联合皮层低灌注:胆碱能功能障碍的潜在指标?
Brain Imaging Behav. 2011 Mar;5(1):25-35. doi: 10.1007/s11682-010-9108-x.
7
Alpha-synuclein aggregation induced by brief ischemia negatively impacts neuronal survival in vivo: a study in [A30P]alpha-synuclein transgenic mouse.短暂缺血诱导的α-突触核蛋白聚集对体内神经元存活产生负面影响:[A30P]α-突触核蛋白转基因小鼠的研究。
J Cereb Blood Flow Metab. 2011 Mar;31(3):913-23. doi: 10.1038/jcbfm.2010.170. Epub 2010 Sep 29.
8
Kallikrein-related peptidase 6 in Alzheimer's disease and vascular dementia.阿尔茨海默病和血管性痴呆中的激肽释放酶相关肽 6。
Brain Res. 2010 Dec 2;1363:1-10. doi: 10.1016/j.brainres.2010.09.017. Epub 2010 Sep 21.
9
Oxidative stress partially contributes to iron-induced α-synuclein aggregation in SK-N-SH cells.氧化应激部分导致铁诱导的 SK-N-SH 细胞中α-突触核蛋白聚集。
Neurotox Res. 2011 Apr;19(3):435-42. doi: 10.1007/s12640-010-9187-x. Epub 2010 Apr 10.
10
Endothelin-converting enzyme-1 in Alzheimer's disease and vascular dementia.阿尔茨海默病和血管性痴呆中的内皮素转化酶-1。
Neuropathol Appl Neurobiol. 2010 Oct;36(6):487-97. doi: 10.1111/j.1365-2990.2010.01084.x. Epub 2010 Mar 22.

路易体痴呆患者枕叶皮质中血管内皮生长因子和毛细血管密度降低。

Reduced vascular endothelial growth factor and capillary density in the occipital cortex in dementia with Lewy bodies.

作者信息

Miners Scott, Moulding Hayley, de Silva Rohan, Love Seth

机构信息

Dementia Research Group, Institute of Clinical Neurosciences, School of Clinical Sciences, University of Bristol, Bristol, UK.

出版信息

Brain Pathol. 2014 Jul;24(4):334-43. doi: 10.1111/bpa.12130. Epub 2014 Mar 28.

DOI:10.1111/bpa.12130
PMID:24521289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8029164/
Abstract

In dementia with Lewy bodies (DLB), blood flow tends to be reduced in the occipital cortex. We previously showed elevated activity of the endothelin and angiotensin pathways in Alzheimer's disease (AD). We have measured endothelin-1 (ET-1) level and angiotensin-converting enzyme (ACE) activity in the occipital cortex in DLB and control brains. We also measured vascular endothelial growth factor (VEGF); factor VIII-related antigen (FVIIIRA) to indicate microvessel density; myelin-associated glycoprotein (MAG), a marker of ante-mortem hypoperfusion; total α-synuclein (α-syn) and α-synuclein phosphorylated at Ser129 (α-syn-p129). In contrast to findings in AD, ACE activity and ET-1 level were unchanged in DLB compared with controls. VEGF and FVIIIRA levels were, however, significantly lower in DLB. VEGF correlated positively with MAG concentration (in keeping with a relationship between reduction in VEGF and hypoperfusion), and negatively with α-syn and α-syn-p129 levels. Both α-syn and α-syn-p129 levels increased in human SH-SY5Y neuroblastoma cells after oxygen-glucose deprivation (OGD), and VEGF level was reduced in SH-SY5Y cells overexpressing α-syn. Taken together, our findings suggest that reduced microvessel density rather than vasoconstriction is responsible for lower occipital blood flow in DLB, and that the loss of microvessels may result from VEGF deficiency, possible secondary to the accumulation of α-syn.

摘要

在路易体痴呆(DLB)中,枕叶皮质的血流往往会减少。我们之前发现阿尔茨海默病(AD)中内皮素和血管紧张素途径的活性升高。我们测量了DLB患者和对照者大脑枕叶皮质中内皮素-1(ET-1)水平和血管紧张素转换酶(ACE)活性。我们还测量了血管内皮生长因子(VEGF);用于指示微血管密度的因子VIII相关抗原(FVIIIRA);髓鞘相关糖蛋白(MAG),一种生前灌注不足的标志物;总α-突触核蛋白(α-syn)和丝氨酸129位点磷酸化的α-突触核蛋白(α-syn-p129)。与AD的研究结果相反,与对照组相比,DLB中的ACE活性和ET-1水平没有变化。然而,DLB中的VEGF和FVIIIRA水平显著降低。VEGF与MAG浓度呈正相关(这与VEGF降低和灌注不足之间的关系一致),与α-syn和α-syn-p129水平呈负相关。在氧糖剥夺(OGD)后,人SH-SY5Y神经母细胞瘤细胞中的α-syn和α-syn-p129水平均升高,而过表达α-syn的SH-SY5Y细胞中的VEGF水平降低。综合来看,我们的研究结果表明,微血管密度降低而非血管收缩是DLB患者枕叶血流降低的原因,微血管的丧失可能是由于VEGF缺乏所致,这可能继发于α-syn的积累。