Proanthocyanidins from the bark of Metasequoia glyptostroboides ameliorate allergic contact dermatitis through directly inhibiting T cells activation and Thl/Th17 responses

被引:23
作者
Chen, Fengyang [1 ]
Ye, Xiaodi [1 ]
Yang, Yadong [2 ]
Teng, Tianli [1 ]
Li, Xiaoyu [1 ]
Xu, Shifang [1 ]
Ye, Yiping [1 ]
机构
[1] Zhejiang Acad Med Sci, Inst Mat Med, Hangzhou 310013, Zhejiang, Peoples R China
[2] Zhejiang Acad Med Sci, Inst Bioengn, Hangzhou 310013, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
Metasequoia glyptostroboides; Proanthocyanidin; Allergic contact dermatitis; T cells activation; Th1/Th17; responses; CONCANAVALIN-A; PROLIFERATION;
D O I
10.1016/j.phymed.2015.03.006
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Objective: The leaves and bark of Metasequoia glyptostroboides are used as anti-microbic, analgesic and anti-inflammatory drug for dermatic diseases in Chinese folk medicine. However, the pharmacological effects and material basis responsible for the therapeutic use of this herb have not yet been well studied. The objectives of this study were to evaluate the anti-inflammatory effects of the proanthocyanidin fraction from the bark of M. glyptostroboides (MGEB) and to elucidate its immunological mechanisms. Materials and methods: The anti-inflammatory activity of MGEB was evaluated using 2,4-dinitrofluorobenzene (DNFB)-induced allergic contact dermatitis (ACD) in mice. Its potential mechanisms were further investigated by determining its effects on Con A-induced T cell activation and Th1/Th17 responses in vitro. Results: Both intraperitoneal injection and oral administration of MGEB significantly reduced the ear swelling in DNFB-induced ACD mice. MGEB inhibited Con A-induced proliferation and the expression levels of cell surface molecules CD69 and CD25 of T cells in vitro. MGEB also significantly decreased the production of Thl/Th17 specific cytokines (IL-2, IFN-gamma and IL-17) and down-regulated theft mRNA expression levels in activated T-cells. Conclusions: MGEB could ameliorate ACD, at least in part, through directly inhibiting T cells activation and Th1/Th17 responses. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:510 / 515
页数:6
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