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苯妥英钠在最佳剂量下通过调节免疫调节细胞改善实验性自身免疫性脑脊髓炎。

Phenytoin at optimum doses ameliorates experimental autoimmune encephalomyelitis via modulation of immunoregulatory cells.

机构信息

Department of Neurology, Kanazawa Medical University, Uchinada, Ishikawa Prefecture 920-0293, Japan.

出版信息

J Neuroimmunol. 2011 Apr;233(1-2):112-9. doi: 10.1016/j.jneuroim.2010.12.006. Epub 2011 Jan 14.

Abstract

We investigated the optimum doses of phenytoin for treatment of myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis (EAE). Oral and intraperitoneal administrations of 0.25 to 1.0mg per mouse (12.5-50mg/kg) 3 times a week improved the clinical course. Intraperitoneal injections of 1.0mg phenytoin were the most effective, as a significant reduction in EAE severity was seen after only 2 administrations with that protocol. Treatment efficacy was associated with amelioration of cellular infiltrates in the CNS, and an increase in CD4(+)Foxp3(+) and CD4(+)CD25(+)CD127(-) regulatory T cells as well as CD8(+) suppressor/cytotoxic T cells in blood.

摘要

我们研究了苯妥英的最佳剂量,以治疗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(EAE)。每周口服或腹腔内给予 0.25 至 1.0mg/只小鼠(12.5-50mg/kg)3 次,可改善临床病程。腹腔内注射 1.0mg 苯妥英是最有效的,因为仅用该方案进行 2 次给药就可显著降低 EAE 严重程度。治疗效果与中枢神经系统中细胞浸润的改善有关,并且血液中的 CD4(+)Foxp3(+)和 CD4(+)CD25(+)CD127(-)调节性 T 细胞以及 CD8(+)抑制/细胞毒性 T 细胞数量增加。

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