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本文引用的文献

1
On the structure and functions of gelatinase B/matrix metalloproteinase-9 in neuroinflammation.关于明胶酶B/基质金属蛋白酶-9在神经炎症中的结构与功能
Prog Brain Res. 2014;214:193-206. doi: 10.1016/B978-0-444-63486-3.00009-8.
2
Matrix metalloproteinase-9: dual role and temporal profile in intracerebral hemorrhage.基质金属蛋白酶-9:在脑出血中的双重作用及时间变化特征
J Stroke Cerebrovasc Dis. 2014 Nov-Dec;23(10):2498-2505. doi: 10.1016/j.jstrokecerebrovasdis.2014.07.005. Epub 2014 Oct 11.
3
Early reperfusion injury is associated to MMP2 and IL-1β elevation in cortical neurons of rats subjected to middle cerebral artery occlusion.早期再灌注损伤与大脑中动脉闭塞大鼠皮质神经元中MMP2和IL-1β升高有关。
Neuroscience. 2014 Sep 26;277:755-63. doi: 10.1016/j.neuroscience.2014.07.064. Epub 2014 Aug 7.
4
Role of matrix metalloproteinases in animal models of ischemic stroke.基质金属蛋白酶在缺血性中风动物模型中的作用。
Curr Vasc Pharmacol. 2015;13(2):161-6. doi: 10.2174/15701611113116660161.
5
Matrix metalloproteinase inhibition in atherosclerosis and stroke.基质金属蛋白酶抑制在动脉粥样硬化和中风中的作用。
Curr Mol Med. 2013 Sep;13(8):1299-313. doi: 10.2174/15665240113139990067.
6
Early inhibition of MMP activity in ischemic rat brain promotes expression of tight junction proteins and angiogenesis during recovery.早期抑制缺血性大鼠脑组织中 MMP 的活性可促进恢复过程中紧密连接蛋白和血管生成的表达。
J Cereb Blood Flow Metab. 2013 Jul;33(7):1104-14. doi: 10.1038/jcbfm.2013.56. Epub 2013 Apr 10.
7
Normobaric hyperoxia combined with minocycline provides greater neuroprotection than either alone in transient focal cerebral ischemia.常压高氧联合米诺环素治疗比单独应用任一方法在短暂性局灶性脑缺血中提供更大的神经保护作用。
Exp Neurol. 2013 Feb;240:9-16. doi: 10.1016/j.expneurol.2012.11.018. Epub 2012 Nov 26.
8
Spatiotemporal evolution of blood brain barrier damage and tissue infarction within the first 3h after ischemia onset.缺血发作后 3h 内血脑屏障损伤和组织梗死的时空演变。
Neurobiol Dis. 2012 Dec;48(3):309-16. doi: 10.1016/j.nbd.2012.07.007. Epub 2012 Jul 17.
9
Intranuclear matrix metalloproteinases promote DNA damage and apoptosis induced by oxygen-glucose deprivation in neurons.核内基质金属蛋白酶促进神经元氧糖剥夺诱导的 DNA 损伤和细胞凋亡。
Neuroscience. 2012 Sep 18;220:277-90. doi: 10.1016/j.neuroscience.2012.06.019. Epub 2012 Jun 16.
10
Inhibition of MMP-9 by a selective gelatinase inhibitor protects neurovasculature from embolic focal cerebral ischemia.选择性明胶酶抑制剂抑制 MMP-9 对栓塞性局灶性脑缺血的神经血管保护作用。
Mol Neurodegener. 2012 May 15;7:21. doi: 10.1186/1750-1326-7-21.

基质金属蛋白酶作为中风的治疗靶点。

Matrix metalloproteinases as therapeutic targets for stroke.

作者信息

Yang Yi, Rosenberg Gary A

机构信息

Department of Neurology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.

Department of Neurology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.

出版信息

Brain Res. 2015 Oct 14;1623:30-8. doi: 10.1016/j.brainres.2015.04.024. Epub 2015 Apr 25.

DOI:10.1016/j.brainres.2015.04.024
PMID:25916577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4569515/
Abstract

Matrix metalloproteinases (MMPs) are important in injury and recovery in ischemic injury. They are proteolytic enzymes that degrade all components of the extracellular matrix (ECM). They are secreted in a latent form, protecting the cell from damage, but once activated induce injury prior to rapid inactivation by four tissue inhibitors to metalloproteinases (TIMPs). Normally the constitutive enzymes, MMP-2 and membrane type MMP (MMP-14), are activated in a spatially specific manner and act close to the site of activation, while the inducible enzymes, MMP-3 and MMP-9, become active through the action of free radicals and other enzymes during neuroinflammation. Because of the complex nature of the interactions with tissues during development, injury and repair, the MMPs have multiple roles, participating in the injury process in the early stages and contributing to recovery during the later stages. This dual role complicates the planning of treatment strategies. This article is part of a Special Issue entitled SI: Cell Interactions In Stroke.

摘要

基质金属蛋白酶(MMPs)在缺血性损伤的损伤和恢复过程中起着重要作用。它们是能够降解细胞外基质(ECM)所有成分的蛋白水解酶。它们以无活性形式分泌,保护细胞免受损伤,但一旦被激活,在被四种金属蛋白酶组织抑制剂(TIMPs)快速失活之前就会引发损伤。正常情况下,组成型酶MMP-2和膜型MMP(MMP-14)以空间特异性方式被激活,并在激活位点附近起作用,而诱导型酶MMP-3和MMP-9在神经炎症期间通过自由基和其他酶的作用而变得活跃。由于在发育、损伤和修复过程中与组织相互作用的复杂性,MMPs具有多种作用,在早期参与损伤过程,在后期有助于恢复。这种双重作用使治疗策略的规划变得复杂。本文是名为“中风中的细胞相互作用”特刊的一部分。