Hyperforin-loaded gold nanoparticle alleviates experimental autoimmune encephalomyelitis by suppressing Th1 and Th17 cells and upregulating regulatory T cells

被引:38
|
作者
Nosratabadi, Reza [1 ]
Rastin, Maryam [2 ]
Sankian, Mojtaba [2 ]
Haghmorad, Dariush [3 ]
Mahmoudi, Mahmoud [2 ]
机构
[1] Rafsanjan Univ Med Sci, Immunol Infect Dis Res Ctr, Rafsanjan, Iran
[2] Mashhad Univ Med Sci, BuAli Res Inst, Sch Med, Immunol Res Ctr, Mashhad, Iran
[3] Semnan Univ Med Sci, Sch Med, Dept Immunol, Semnan, Iran
关键词
Hyperforin; Multiple sclerosis; Experimental autoimmune encephalomyelitis (EAE); Myelin oligodendrocyte glycoprotein (MOG); Gold nanoparticle; ST-JOHNS-WORT; NF-KAPPA-B; MULTIPLE-SCLEROSIS; IN-VIVO; DIFFERENTIATION; INFLAMMATION; CYTOKINES; DISEASE; ANTIOXIDANT; MODEL;
D O I
10.1016/j.nano.2016.04.001
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Hyperforin an herbal compound, is commonly used in traditional medicine due to its anti-inflammatory activities. The aim of this study was to use a hyperforin loaded gold nanoparticle ( Hyp-GNP) in the treatment of experimental autoimmune encephalomyelitis ( EAE) an animal model of multiple sclerosis ( MS). Hyp-GNP and hyperforin significantly reduced clinical severity of EAE, which was accompanied by a decrease in the number of inflammatory cell infiltration in the spinal cord. Additionally, treatment with Hyp-GNP significantly inhibited disease-associated cytokines as well as an increase in the anti-inflammatory cytokines in comparison to all groups including the free-hyp group. Furthermore, hyperforin and Hyp-GNP inhibited the differentiation of Th1 and Th17 cells while promoting Treg and Th2 cell differentiation via regulating their master transcription factors. The current study demonstrated the although, free-hyp improved clinical and laboratory data Hyp-GNP is significantly more efficient than free hyperforin in the treatment of EAE. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1961 / 1971
页数:11
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