Department of Neurology, St Josef Hospital, Ruhr-University Bochum, D-44791 Bochum, Germany.
Brain. 2011 Mar;134(Pt 3):678-92. doi: 10.1093/brain/awq386.
Inflammation and oxidative stress are thought to promote tissue damage in multiple sclerosis. Thus, novel therapeutics enhancing cellular resistance to free radicals could prove useful for multiple sclerosis treatment. BG00012 is an oral formulation of dimethylfumarate. In a phase II multiple sclerosis trial, BG00012 demonstrated beneficial effects on relapse rate and magnetic resonance imaging markers indicative of inflammation as well as axonal destruction. First we have studied effects of dimethylfumarate on the disease course, central nervous system, tissue integrity and the molecular mechanism of action in an animal model of chronic multiple sclerosis: myelin oligodendrocyte glycoprotein induced experimental autoimmune encephalomyelitis in C57BL/6 mice. In the chronic phase of experimental autoimmune encephalomyelitis, preventive or therapeutic application of dimethylfumarate ameliorated the disease course and improved preservation of myelin, axons and neurons. In vitro, the application of fumarates increased murine neuronal survival and protected human or rodent astrocytes against oxidative stress. Application of dimethylfumarate led to stabilization of the transcription factor nuclear factor (erythroid-derived 2)-related factor 2, activation of nuclear factor (erythroid-derived 2)-related factor 2-dependent transcriptional activity and accumulation of NADP(H) quinoline oxidoreductase-1 as a prototypical target gene. Furthermore, the immediate metabolite of dimethylfumarate, monomethylfumarate, leads to direct modification of the inhibitor of nuclear factor (erythroid-derived 2)-related factor 2, Kelch-like ECH-associated protein 1, at cysteine residue 151. In turn, increased levels of nuclear factor (erythroid-derived 2)-related factor 2 and reduced protein nitrosylation were detected in the central nervous sytem of dimethylfumarate-treated mice. Nuclear factor (erythroid-derived 2)-related factor 2 was also upregulated in the spinal cord of autopsy specimens from untreated patients with multiple sclerosis. In dimethylfumarate-treated mice suffering from experimental autoimmune encephalomyelitis, increased immunoreactivity for nuclear factor (erythroid-derived 2)-related factor 2 was detected by confocal microscopy in neurons of the motor cortex and the brainstem as well as in oligodendrocytes and astrocytes. In mice deficient for nuclear factor (erythroid-derived 2)-related factor 2 on the same genetic background, the dimethylfumarate mediated beneficial effects on clinical course, axon preservation and astrocyte activation were almost completely abolished thus proving the functional relevance of this transcription factor for the neuroprotective mechanism of action. We conclude that the ability of dimethylfumarate to activate nuclear factor (erythroid-derived 2)-related factor 2 may offer a novel cytoprotective modality that further augments the natural antioxidant responses in multiple sclerosis tissue and is not yet targeted by other multiple sclerosis therapies.
炎症和氧化应激被认为可促进多发性硬化症中的组织损伤。因此,增强细胞对自由基抵抗力的新型治疗药物可能对多发性硬化症的治疗有用。BG00012 是富马酸二甲酯的口服制剂。在一项多发性硬化症的 II 期临床试验中,BG00012 显示出对复发率和磁共振成像标记物(表明炎症和轴突破坏)有益的效果。首先,我们在慢性多发性硬化症的动物模型中研究了富马酸二甲酯对疾病进程、中枢神经系统、组织完整性和作用机制的影响:髓鞘少突胶质细胞糖蛋白诱导的实验性自身免疫性脑脊髓炎在 C57BL/6 小鼠中。在实验性自身免疫性脑脊髓炎的慢性期,富马酸二甲酯的预防性或治疗性应用可改善疾病进程并改善髓鞘、轴突和神经元的保存。体外,富马酸盐的应用可增加鼠神经元的存活,并保护人或啮齿动物星形胶质细胞免受氧化应激的影响。富马酸二甲酯的应用导致转录因子核因子(红系衍生 2)相关因子 2 的稳定化,核因子(红系衍生 2)相关因子 2 依赖性转录活性的激活以及 NADP(H)醌氧化还原酶-1 的积累作为典型的靶基因。此外,富马酸二甲酯的直接代谢物,单甲基富马酸,导致核因子(红系衍生 2)相关因子 2 的抑制剂 Kelch 样 ECH 相关蛋白 1 的半胱氨酸残基 151 的直接修饰。反过来,在富马酸二甲酯处理的小鼠的中枢神经系统中检测到核因子(红系衍生 2)相关因子 2 水平升高和蛋白质亚硝化为减少。核因子(红系衍生 2)相关因子 2 也在未经治疗的多发性硬化症患者的尸检标本的脊髓中上调。在患有实验性自身免疫性脑脊髓炎的富马酸二甲酯治疗的小鼠中,通过共聚焦显微镜检测到运动皮层和脑干中的神经元以及少突胶质细胞和星形胶质细胞中的核因子(红系衍生 2)相关因子 2 的免疫反应性增加。在具有相同遗传背景的核因子(红系衍生 2)相关因子 2 缺陷的小鼠中,富马酸二甲酯对临床病程、轴突保存和星形胶质细胞激活的有益作用几乎完全被消除,从而证明了该转录因子对神经保护作用机制的功能相关性。我们得出结论,富马酸二甲酯激活核因子(红系衍生 2)相关因子 2 的能力可能提供一种新的细胞保护方式,进一步增强多发性硬化症组织中的天然抗氧化反应,并且尚未被其他多发性硬化症治疗方法靶向。
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