Combined treatment with atorvastatin and minocycline suppresses severity of EAE

被引:46
作者
Luccanini, Ilaria [1 ]
Ballerini, Clara [2 ]
Blagioli, Tiziana [2 ]
Biamonte, Filippo [3 ]
Bellucci, Arianna [4 ]
Rosi, Maria Cristina [1 ]
Grossi, Cristina [1 ]
Massacesi, Luca [2 ]
Casamenti, Fiorella [1 ]
机构
[1] Univ Florence, Dept Pharmacol, I-50139 Florence, Italy
[2] Univ Florence, Dept Neurol, I-50139 Florence, Italy
[3] Lab Dev Neurosci, I-00128 Rome, Italy
[4] Univ Brescia, Dept Biomed & Biotechnol, I-25123 Brescia, Italy
关键词
minocycline; atorvastatin; minocycline and atorvastatin in combination; mice; experimental autoimmune encephalomyelitis; anti-myelin oligodendrocyte protein antibodies; neuroprotection;
D O I
10.1016/j.expneurol.2008.01.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Multiple sclerosis (MS) is the most common inflammatory demyelinating disorder of the central nervous system (CNS). An approach to improve MS treatment is to identify a rational combination of new medications or existing therapies that impact different aspects of the disease process. Statins are effective in the treatment of MS animal models and are promising candidates for future treatment. Minocycline ameliorates clinical severity of experimental autoimmune encephalomyelitis (EAE) and exhibits several anti-inflammatory and neuroprotective activities. In this study, we tested whether the combination of these two drugs could produce beneficial effects in EAE mice immunized with myelin oligodendrocyte protein (MOG). Our findings show that combined treatment, compared to using the medications alone, resulted in a significant reduction in disease severity, in both the acute and chronic phases of the disease, along with attenuation of inflammation, demyclination and axonal loss. Stereological analysis revealed that the combined treatment significantly guarded against neuroinflammation and neurodegeneration. Moreover, a significant suppression of anti-MOG antibody production in animals treated with the two medications was found. In conclusion, our findings prove that this combination of drugs is neuroprotective and suppresses the severity of EAE. Furthermore, this pharmacological approach appears to be promising as a future therapeutic strategy to control MS. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:214 / 226
页数:13
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