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阿托伐他汀和全反式维甲酸协同改善多发性硬化症动物模型。

Synergistic effects of atorvastatin and all-trans retinoic acid in ameliorating animal model of multiple sclerosis.

机构信息

Assistant Professor of Immunology, Department of Microbiology .

出版信息

Immunol Invest. 2014;43(1):54-68. doi: 10.3109/08820139.2013.825269. Epub 2013 Sep 24.

Abstract

One suitable approach to enhancing multiple sclerosis (MS) treatment is combination of available medications to provide more desirable outcomes. Immunomodulatory effects of atorvastatin and/or all-trans retinoic acid (ATRA) were determined in previous studies. The present study was set out to investigate the synergistic effects of combination therapy by suboptimal doses of atorvastatin and ATRA in experimental autoimmune encephalomyelitis (EAE), an animal model of MS. EAE was induced by MOG35-55 in female C57BL/6 mice. Therapies were initiated at day 12 post immunization when the mice developed a disability score and continued throughout the study until the day 33 when animals were sacrificed. Therapeutic treatment with half doses of atorvastatin and ATRA in combination has synergistic benefits causing the regression of clinical and neuropathological features of EAE more favorable than treatment with full doses of either drug alone. Without any advantage in anti-proliferative effect, combination treatment significantly reduced the secretion of pro-inflammatory cytokine interleukin-17 and conversely, increased the production of anti-inflammatory cytokine interleukin-10 more prominent than either drug alone. Furthermore, FoxP3+Treg cells were significantly increased only in combination treatment. In conclusion, combined atorvastatin and ATRA have immunomodulatory synergistic benefits and this pharmacological approach may be as a useful strategy to control MS.

摘要

一种增强多发性硬化症(MS)治疗的合适方法是将现有药物联合使用,以获得更理想的结果。先前的研究已经确定了阿托伐他汀和/或全反式视黄酸(ATRA)的免疫调节作用。本研究旨在研究亚治疗剂量的阿托伐他汀和 ATRA 联合治疗实验性自身免疫性脑脊髓炎(EAE),即 MS 动物模型的协同作用。在雌性 C57BL/6 小鼠中通过 MOG35-55 诱导 EAE。在免疫后第 12 天开始治疗,此时小鼠出现残疾评分,并持续整个研究过程,直到第 33 天处死动物。阿托伐他汀和 ATRA 的半剂量联合治疗具有协同作用,可使 EAE 的临床和神经病理学特征消退,比单独使用全剂量药物更有利。联合治疗在没有任何增殖抑制作用优势的情况下,显著降低了促炎细胞因子白细胞介素-17 的分泌,相反,增加了抗炎细胞因子白细胞介素-10 的产生,比单独使用任何一种药物都更明显。此外,只有联合治疗才会显著增加 FoxP3+Treg 细胞。总之,阿托伐他汀和 ATRA 的联合使用具有免疫调节协同作用,这种药理学方法可能是控制 MS 的一种有用策略。

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