Department of Neurology, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Department of Health Development and Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka, 565-0871, Japan.
Neurotherapeutics. 2021 Jan;18(1):460-473. doi: 10.1007/s13311-020-00948-w. Epub 2020 Oct 20.
Go-sha-jinki-Gan (GJG) is a traditional Japanese herbal medicine. In clinical practice, GJG is effective against neuropathic pain and hypersensitivity induced by chemotherapy or diabetes. In our previous study using a chronic constriction injury mouse model, we showed that GJG inhibited microglia activation by suppressing the expression of tumor necrosis factor-α (TNF-α) and p38 mitogen-activated protein kinase (p38 MAPK) in the peripheral nervous system. To investigate whether GJG can suppress inflammation in the central nervous system (CNS) in the context of neurological disorders, we examined the effect of GJG on the activation of resident glial cells and on p38-TNF signaling in two mouse models of neurological disorders: the experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis and the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of Parkinson's disease. GJG administration relieved the severity of clinical EAE symptoms and MPTP-induced inflammation by decreasing the number of microglia and the production of TNF-α in the spinal cord of EAE mice and the substantia nigra of MPTP-treated mice. Accordingly, GJG suppressed the phosphorylation of p38 in glial cells of these two mouse models. We conclude that GJG attenuates inflammation of the CNS by suppressing glial cell activation, followed by a decrease in the production of TNF-α via p38-TNF signaling.
葛根芩连汤是一种传统的日本草药。在临床实践中,葛根芩连汤对化疗或糖尿病引起的神经病理性疼痛和超敏反应有效。在我们之前使用慢性缩窄损伤小鼠模型的研究中,我们表明葛根芩连汤通过抑制肿瘤坏死因子-α(TNF-α)和丝裂原活化蛋白激酶 p38(p38 MAPK)在外周神经系统中的表达来抑制小胶质细胞激活。为了研究葛根芩连汤是否可以抑制神经紊乱时中枢神经系统(CNS)的炎症,我们研究了葛根芩连汤对两种神经紊乱小鼠模型中神经胶质细胞激活和 p38-TNF 信号的影响:多发性硬化的实验性自身免疫性脑脊髓炎(EAE)模型和帕金森病的 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)模型。葛根芩连汤通过减少 EAE 小鼠脊髓和 MPTP 处理小鼠黑质中小胶质细胞数量和 TNF-α的产生,缓解了 EAE 症状的严重程度和 MPTP 诱导的炎症。相应地,葛根芩连汤抑制了这两种小鼠模型中神经胶质细胞中 p38 的磷酸化。我们得出结论,葛根芩连汤通过抑制神经胶质细胞激活来减轻 CNS 炎症,随后通过 p38-TNF 信号减少 TNF-α的产生。