[1] Simon DW, Mcgeachy MJ, Bayir H, et al. The far-reaching scope of neuroinflammation after traumatic brain injury[J]. Nat Rev Neurol, 2017, 13:171-191. [2] Pietro VD, Ragusa M, Davies D, et al. microRNAs as novel biomarkers for the diagnosis and prognosis of mild and severe traumatic brain injury[J]. J Neurotrauma, 2017, 34:1948-1956. [3] 逯冉冉, 耿建红, 张群英,等. 白藜芦醇预处理介导Wnt/β-catenin信号通路保护脑缺血再灌注大鼠海马区神经元损伤[J]. 神经解剖学杂志, 2017, 33:611-616. [4] Zhang P, Li H, Yang B, et al. Biological significance and therapeutic implication of resveratrol-inhibited Wnt, Notch and STAT3 signaling in cervical cancer cells[J]. Genes Cancer, 2014, 5:154-164. [5] Tanriverdi G, Kaya-Dagistanli F, Ayla S, et al. Resveratrol can prevent CCl4-induced liver injury by inhibiting Notch signaling pathway[J]. Histol Histopathol, 2016, 31:769-784. [6] 甘晓, 张东波, 刘向业, 等. 脉冲磁场对颅脑损伤脑组织中内源性神经干细胞因子的影响[J]. 中国组织工程研究, 2017, 21:3376-3381. [7] 余萍萍. 白藜芦醇对大鼠脑缺血/再灌注损伤后星形胶质细胞活化的影响[J]. 中国药理学通报, 2015, 31:1228-1233. [8] 张涛, 国建飞, 邢琳琳,等. 塞来昔布对颅脑创伤后大鼠的凋亡蛋白Bcl-2和Bax表达影响[J]. 中国临床药理学杂志, 2017, 33:813-816. [9] Berman AY, Motechin RA, Wiesenfeld MY, et al. The therapeutic potential of resveratrol: a review of clinical trials[J]. NPJ Precis Oncol, 2017, 1:35-43. [10] 张莉峰, 滕军放, 袁学谦, 等. 白藜芦醇通过抑制TNF-α表达保护大鼠脑缺血再灌注损伤[J]. 中国动脉硬化杂志, 2017, 25:32-36. [11] Xu X, Jiang R, Gong P, et al. Up-regulation of FOS-like antigen 1 contributes to neuronal apoptosis in the cortex of rat following traumatic brain injury[J]. Metab Brain Dis, 2017, 33:115-125. [12] Ji W, Liu H, Liu C, et al. Up-regulation of MCM3 relates to neuronal apoptosis after traumatic brain injury in adult rats[J]. Cell Mol Neurobiol, 2017, 37:683-693. [13] Evans LP, Newell EA, Mahajan MA, et al. Acute vitreoretinal trauma and inflammation after traumatic brain injury in mice[J]. Ann Clin Transl Neurol, 2018, 5:240-251. [14] Siebel C, Lendahl U. Notch signaling in development, tissue homeostasis, and disease[J]. Physiol Rev, 2017, 97:1235-1294. [15] Yin J, Li H, Feng C, et al. Inhibition of brain ischemia-caused notch activation in microglia may contribute to isoflurane postconditioning-induced neuroprotection in male rats[J]. CNS Neurol Disord Drug Targets, 2014, 13:718-732. |