Zhang Zhen, Zhang Ze, Lu Hong, Yang Qingwu, Wu He, Wang Jian
Department of Pathology, First Clinical Hospital, Harbin Medical University, Harbin, China.
Department of Urology, First Clinical Hospital, Harbin Medical University, Harbin, China.
Mol Neurobiol. 2017 Apr;54(3):1874-1886. doi: 10.1007/s12035-016-9785-6. Epub 2016 Feb 19.
Intracerebral hemorrhage (ICH) is a subtype of stroke with high mortality and morbidity. When a diseased artery within the brain bursts, expansion and absorption of the resulting hematoma trigger a series of reactions that cause primary and secondary brain injury. Microglia are extremely important for removing the hematoma and clearing debris, but they are also a source of ongoing inflammation. This article discusses the role of microglial activation/polarization and related inflammatory mediators, such as Toll-like receptor 4, matrix metalloproteinases, high-mobility group protein box-1, nuclear factor erythroid 2-related factor 2, heme oxygenase, and iron, in secondary injury after ICH and highlights the potential targets for ICH treatment.
脑出血(ICH)是一种具有高死亡率和高发病率的中风亚型。当脑内病变动脉破裂时,血肿的扩大和吸收会引发一系列导致原发性和继发性脑损伤的反应。小胶质细胞对于清除血肿和清除碎片极为重要,但它们也是持续炎症的来源。本文讨论了小胶质细胞激活/极化以及相关炎症介质,如Toll样受体4、基质金属蛋白酶、高迁移率族蛋白盒1、核因子红细胞2相关因子2、血红素加氧酶和铁,在脑出血后继发性损伤中的作用,并强调了脑出血治疗的潜在靶点。