Wang Yuxi, Yang Yi, Zhang Siran, Li Chengtan, Zhang Lihui
Department of Pharmacology, Hangzhou Key Laboratory of Medical Neurobiology, School of Medicine, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Department of Neurology, Zhejiang Hospital, Hangzhou, Zhejiang, China.
Neurobiol Aging. 2020 Mar;87:1-10. doi: 10.1016/j.neurobiolaging.2019.12.013. Epub 2019 Dec 20.
Neuroinflammation is a complex biological process and has been known to play an important role in age-related cerebrovascular and neurodegenerative disorders, such as cerebral ischemia, Alzheimer's disease, and Parkinson's disease. Cysteinyl leukotrienes (CysLTs) are potent inflammatory lipid mediators that exhibit actions mainly through activating type 1 and type 2 CysLT receptors (CysLT1 and CysLT2). Accumulating evidence shows that CysLT1 and CysLT2 are activated at different stages of pathological process in various cell types in the brain such as vascular endothelial cells, astrocytes, microglia, and neurons in response to insults. However, the precise roles and mechanisms of CysLT1 and CysLT2 in regulating the pathogenesis of cerebral ischemia, Alzheimer's disease, and Parkinson's disease are not fully understood. In this article, we focus on current advances that link activation of CysLT1 and CysLT2 to the pathological process during brain ischemia and neurodegeneration and discuss mechanisms by which CysLT1 and CysLT2 mediate inflammatory process and brain injury. Multitarget anti-inflammatory potentials of CysLT1 and CysLT2 antagonism for neuroinflammation and brain injury will also be reviewed.
神经炎症是一个复杂的生物学过程,已知在与年龄相关的脑血管和神经退行性疾病中起重要作用,如脑缺血、阿尔茨海默病和帕金森病。半胱氨酰白三烯(CysLTs)是强效的炎症性脂质介质,主要通过激活1型和2型半胱氨酰白三烯受体(CysLT1和CysLT2)发挥作用。越来越多的证据表明,在大脑中的各种细胞类型(如血管内皮细胞、星形胶质细胞、小胶质细胞和神经元)对损伤作出反应的病理过程的不同阶段,CysLT1和CysLT2会被激活。然而,CysLT1和CysLT2在调节脑缺血、阿尔茨海默病和帕金森病发病机制中的精确作用和机制尚未完全明了。在本文中,我们重点关注将CysLT1和CysLT2的激活与脑缺血和神经退行性变期间的病理过程联系起来的当前进展,并讨论CysLT1和CysLT2介导炎症过程和脑损伤的机制。还将综述CysLT1和CysLT2拮抗作用对神经炎症和脑损伤的多靶点抗炎潜力。