Department of Pharmacology, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Department of Environmental Sciences, Faculty of Agriculture, Dalhousie University, Truro, Nova Scotia, Canada.
J Neuroimmunol. 2014 Mar 15;268(1-2):71-83. doi: 10.1016/j.jneuroim.2014.01.007. Epub 2014 Jan 21.
The anti-inflammatory and restorative effects of the flavonoid-enriched fraction AF4 were examined in a mouse model of experimental autoimmune encephalomyelitis (EAE). Relative to EAE mice that received vehicle (water, 10 ml/kg/day), oral administration of AF4 (25mg/kg/day) beginning 24h after the onset of clinical signs reduced disease severity from days 19-31 post-immunization. AF4-mediated recovery from EAE was preceded by reduced plasma concentrations of TNFα and IL-1β on day 18 followed by decreased cytokine production and neuropathology in the cerebellum and spinal cord on day 31. Clinical improvement for EAE-AF4 mice from days 18 to 31 was accompanied by the elevated expression of genes that mediate remyelination. These findings suggest that AF4 decreased EAE severity by promoting the resolution of inflammation and improving functional recovery in the CNS.
黄酮富集部分 AF4 在实验性自身免疫性脑脊髓炎(EAE)小鼠模型中表现出抗炎和修复作用。与接受载体(水,10ml/kg/天)的 EAE 小鼠相比,从临床症状出现后 24 小时开始口服 AF4(25mg/kg/天)可降低免疫后 19-31 天的疾病严重程度。AF4 介导的 EAE 恢复是由 18 日血浆 TNFα 和 IL-1β 浓度降低引起的,随后在 31 日小脑和脊髓中的细胞因子产生和神经病理学减少。EAE-AF4 小鼠从第 18 天到第 31 天的临床改善伴随着介导髓鞘再生的基因表达升高。这些发现表明,AF4 通过促进炎症消退和改善中枢神经系统的功能恢复来降低 EAE 的严重程度。