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imaging biomarkers of neuroinflammation in the development and assessment of stroke therapies - towards clinical translation.神经炎症的影像学生物标志物在中风治疗的开发和评估中的应用——走向临床转化。
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本文引用的文献

1
Ischemic stroke intervention requires mixed cellular protection of the penumbra.缺血性中风干预需要对半暗带进行混合细胞保护。
Curr Opin Investig Drugs. 2009 Mar;10(3):220-3.
2
Inflammation markers and prediction of post-stroke vascular disease recurrence: the MITICO study.炎症标志物与中风后血管疾病复发的预测:MITICO研究
J Neurol. 2009 Feb;256(2):217-24. doi: 10.1007/s00415-009-0058-4. Epub 2009 Feb 27.
3
Post-ischemic brain damage: pathophysiology and role of inflammatory mediators.缺血后脑损伤:病理生理学及炎症介质的作用
FEBS J. 2009 Jan;276(1):13-26. doi: 10.1111/j.1742-4658.2008.06766.x.
4
Injuries to the vascular endothelium: vascular wall and endothelial dysfunction.血管内皮损伤:血管壁与内皮功能障碍。
Rev Neurol Dis. 2008;5 Suppl 1:S4-11.
5
In vivo imaging of the inflammatory receptor CD40 after cerebral ischemia using a fluorescent antibody.使用荧光抗体对脑缺血后炎症受体CD40进行体内成像。
Stroke. 2008 Oct;39(10):2845-52. doi: 10.1161/STROKEAHA.107.509844. Epub 2008 Jul 17.
6
Magnetic resonance imaging of endothelial adhesion molecules in mouse atherosclerosis using dual-targeted microparticles of iron oxide.使用双靶向氧化铁微粒对小鼠动脉粥样硬化中内皮黏附分子进行磁共振成像。
Arterioscler Thromb Vasc Biol. 2008 Jan;28(1):77-83. doi: 10.1161/ATVBAHA.107.145466. Epub 2007 Oct 25.
7
In vivo magnetic resonance imaging of acute brain inflammation using microparticles of iron oxide.利用氧化铁微粒对急性脑炎症进行体内磁共振成像。
Nat Med. 2007 Oct;13(10):1253-8. doi: 10.1038/nm1631. Epub 2007 Sep 23.
8
Preconditioning suppresses inflammation in neonatal hypoxic ischemia via Akt activation.预处理通过激活Akt抑制新生儿缺氧缺血中的炎症反应。
Stroke. 2007 Mar;38(3):1017-24. doi: 10.1161/01.STR.0000258102.18836.ca. Epub 2007 Feb 1.
9
Improved regional cerebral blood flow is important for the protection seen in a mouse model of late phase ischemic preconditioning.改善局部脑血流对于在晚期缺血预处理小鼠模型中所观察到的保护作用很重要。
Brain Res. 2006 Nov 22;1121(1):231-7. doi: 10.1016/j.brainres.2006.08.107. Epub 2006 Sep 29.
10
Prevention of inflammation is a mechanism of preconditioning-induced neuroprotection against focal cerebral ischemia.预防炎症是预处理诱导的针对局灶性脑缺血的神经保护机制。
Neurochem Int. 2006 Jul;49(2):127-35. doi: 10.1016/j.neuint.2006.02.011. Epub 2006 Jun 6.

脑缺血小鼠模型中急性血管细胞黏附分子-1 表达的分子磁共振成像。

Molecular magnetic resonance imaging of acute vascular cell adhesion molecule-1 expression in a mouse model of cerebral ischemia.

机构信息

Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.

出版信息

J Cereb Blood Flow Metab. 2010 Jun;30(6):1178-87. doi: 10.1038/jcbfm.2009.287. Epub 2010 Jan 20.

DOI:10.1038/jcbfm.2009.287
PMID:20087364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2949202/
Abstract

The pathogenesis of stroke is multifactorial, and inflammation is thought to have a critical function in lesion progression at early time points. Detection of inflammatory processes associated with cerebral ischemia would be greatly beneficial in both designing individual therapeutic strategies and monitoring outcome. We have recently developed a new approach to imaging components of the inflammatory response, namely endovascular adhesion molecule expression on the brain endothelium. In this study, we show specific imaging of vascular cell adhesion molecule (VCAM)-1 expression in a mouse model of middle cerebral artery occlusion (MCAO), and a reduction in this inflammatory response, associated with improved behavioral outcome, as a result of preconditioning. The spatial extent of VCAM-1 expression is considerably greater than the detectable lesion using diffusion-weighted imaging (25% versus 3% total brain volume), which is generally taken to reflect the core of the lesion at early time points. Thus, VCAM-1 imaging seems to reveal both core and penumbral regions, and our data implicate VCAM-1 upregulation and associated inflammatory processes in the progression of penumbral tissue to infarction. Our findings indicate that such molecular magnetic resonance imaging (MRI) approaches could be important clinical tools for patient evaluation, acute monitoring of therapy, and design of specific treatment strategies.

摘要

中风的发病机制是多因素的,炎症被认为在早期病变进展中起着关键作用。检测与脑缺血相关的炎症过程将极大地有益于设计个体化治疗策略和监测结果。我们最近开发了一种新的方法来对炎症反应的成分进行成像,即血管内皮细胞上的血管细胞黏附分子(VCAM-1)的表达。在这项研究中,我们显示了在大脑中动脉闭塞(MCAO)的小鼠模型中,血管细胞黏附分子(VCAM-1)表达的特异性成像,以及炎症反应的减少与预处理相关的行为结果的改善。VCAM-1 表达的空间范围明显大于弥散加权成像(DWI)检测到的病变范围(25%总脑体积与 3%),DWI 通常被认为反映了早期病变的核心区域。因此,VCAM-1 成像似乎揭示了核心和半影区,我们的数据表明 VCAM-1 的上调和相关炎症过程参与了半影区组织向梗死的进展。我们的发现表明,这种分子磁共振成像(MRI)方法可能是评估患者、急性监测治疗和设计特定治疗策略的重要临床工具。