Preclinical and clinical research on inflammation after intracerebral hemorrhage

被引:601
作者
Wang, Jian [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Anesthesiol Crit Care Med, Baltimore, MD 21205 USA
关键词
Heme oxygenase; Hemorrhagic stroke; Leukocytes; Matrix Metalloproteinase; Microglia; NF E2 related factor 2; Iron; INDUCED BRAIN-INJURY; MATRIX-METALLOPROTEINASE EXPRESSION; DELAYED MINOCYCLINE TREATMENT; FIBRILLARY ACIDIC PROTEIN; STEM-CELL TRANSPLANTATION; ACTIVATED-RECEPTOR-GAMMA; FOCAL CEREBRAL-ISCHEMIA; AUTOLOGOUS WHOLE-BLOOD; TUFTSIN FRAGMENT 1-3; HEME OXYGENASE-1;
D O I
10.1016/j.pneurobio.2010.08.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Intracerebral hemorrhage (ICH) is one of the most lethal stroke subtypes Despite the high morbidity and mortality associated with ICH its pathophysiology has not been investigated as well as that of ischemic stroke Available evidence from preclinical and clinical studies suggests that inflammatory mechanisms are involved in the progression of ICH-induced secondary brain injury For example in preclinical ICH models microglial activation has been shown to occur within 1 h much earlier than neutrophil infiltration Recent advances in our understanding of neuroinflammatory pathways have revealed several new molecular targets and related therapeutic strategies have been tested in preclinical ICH models This review summarizes recent progress made in preclinical models of ICH surveys preclinical and clinical studies of inflammatory cells (leukocytes macrophages microglia and astrocytes) and inflammatory mediators (matrix metalloproteinases nuclear factor erythroid 2-related factor 2 heme oxygenase and iron) and highlights the emerging areas of therapeutic promise (C) 2010 Elsevier Ltd All rights reserved
引用
收藏
页码:463 / 477
页数:15
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