Hispidulin alleviates 2,4-dinitrochlorobenzene and house dust mite extract-induced atopic dermatitis-like skin inflammation

被引:14
作者
Kang, Jinjoo [1 ]
Lee, Soyoung [2 ]
Kim, Namkyung [1 ]
Dhakal, Hima [1 ]
Choi, Young-Ae [1 ]
Kwon, Taeg Kyu [3 ]
Khang, Dongwoo [4 ]
Kim, Sang-Hyun [1 ]
机构
[1] Kyungpook Natl Univ, Cell & Matrix Res Inst, Sch Med, Dept Pharmacol, Daegu, South Korea
[2] Korea Res Inst Biosci & Biotechnol, Immunoregulatory Mat Res Ctr, Jeongeup, South Korea
[3] Keimyung Univ, Sch Med, Dept Immunol, Daegu, South Korea
[4] Gachon Univ, Sch Med, Dept Physiol, Incheon, South Korea
基金
新加坡国家研究基金会;
关键词
Atopic dermatitis; Hispidulin; House dust mite; Keratinocytes; CELLS; ACTIVATION; EOSINOPHILS; RECRUITMENT; MACROPHAGES; CYTOKINES; DELIVERY; EOTAXIN; ALLERGY; PHASE;
D O I
10.1016/j.biopha.2021.111359
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Atopic dermatitis (AD) is a chronic inflammatory skin disorder that affects 10?20% of the world?s population. Therefore, the discovery of drugs for the treatment of AD is important for human health. Hispidulin (HPD; also known as scutellarein 6-methyl ether or dinatin) is a natural flavone that exerts anti-inflammatory effects. In the present study, the effectiveness of HPD on AD-like skin inflammation was investigated. We used a mouse AD model through repeated exposure of mice to 2,4-dinitrochlorobenzene and house dust mite extract (Dermato-phagoides farinae extract, DFE) to the ears. In addition, tumor necrosis factor-? and interferon-?-activated ker-atinocytes (HaCaT cells) were used to investigate the underlying mechanism of HPD action. Oral administration of HPD alleviated AD-like skin inflammations: it reduced ear thickness; serum immunoglobulin (Ig)E, DFE-specific IgE, and IgG2a levels; and inflammatory cell infiltration. HPD reduced the expression of pro-inflammatory cytokines and chemokines through inhibition of signal transducer and activator of transcription 1 nuclear factor-?B in HaCaT cells. Taken together, these results suggest that HPD could be a potential drug candidate for the treatment of AD.
引用
收藏
页数:8
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