Department of Neurosurgery, Qilu Hospital of Shandong University and Brain Science Research Institute, Shandong University, Key Laboratory of Brain Functional Remodeling, Shandong, 107# Wenhua Xi Road, Jinan 250012, China.
K.G. Jebsen Brain Tumor Research Center, Department of Biomedicine, University of Bergen, Jonas Lies vei 91, 5009 Bergen, Norway.
Life Sci. 2020 May 15;249:117542. doi: 10.1016/j.lfs.2020.117542. Epub 2020 Mar 10.
Sphingosine-1-phosphate (S1P) is a bioactive sphingolipid that regulates lymphocyte trafficking, glial cell activation, vasoconstriction, endothelial barrier function, and neuronal death pathways in the brain. Research has increasingly implicated S1P in the pathology of cerebral ischemia reperfusion (IR) injury. As a high-affinity agonist of S1P receptor, fingolimod exhibits excellent neuroprotective effects against ischemic challenge both in vivo and in vitro. By summarizing recent progress on how S1P participates in the development of brain IR injury, this review identifies potential therapeutic targets for the treatment of brain IR injury.
鞘氨醇-1-磷酸(S1P)是一种生物活性鞘脂,可调节淋巴细胞的迁移、神经胶质细胞的激活、血管收缩、内皮屏障功能和大脑中的神经元死亡途径。研究越来越多地表明 S1P 参与了脑缺血再灌注(IR)损伤的发病机制。作为 S1P 受体的高亲和力激动剂,芬戈莫德在体内和体外对缺血性刺激均表现出优异的神经保护作用。通过总结 S1P 参与脑 IR 损伤发展的最新进展,本综述确定了治疗脑 IR 损伤的潜在治疗靶点。