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紫草素抑制特应性皮炎患者树突状细胞中Der p 2诱导的细胞因子和趋化因子表达。

Shikonin Inhibits Der p 2-Induced Cytokine and Chemokine Expression in Dendritic Cells in Patients with Atopic Dermatitis.

作者信息

Yen Chung-Yang, Chiang Wen-Dee, Liu Shang-Yong, Yu Sheng-Jie, Hsieh Ching-Liang

机构信息

Department of Dermatology, Taichung Veterans General Hospital, Taichung 40705, Taiwan.

Department of Food Science, Tunghai University, Taichung 40704, Taiwan.

出版信息

Evid Based Complement Alternat Med. 2020 Jul 31;2020:9506363. doi: 10.1155/2020/9506363. eCollection 2020.

Abstract

Atopic dermatitis (AD) is a common inflammatory skin disorder. Shikonin, the active component of extract, exhibits anti-inflammatory effects. The objective of the present study was to investigate the effect of shikonin on proinflammatory cytokines and chemokine in patients with AD. Ten patients with AD who were allergic to house dust mite (HDM) and seven healthy controls were recruited in this study. Peripheral blood mononuclear cells were isolated, and CD14 cells were further selected and differentiated to dendritic cells. Dendritic cells stimulated using Der p 2, the major HDM allergen, were cotreated with shikonin for 24 hours, and dexamethasone was used as a control. Culture supernatants were collected, and proinflammatory cytokine and chemokine concentrations were analyzed using a multiplex assay system. Shikonin significantly inhibited Der p 2-induced expression of interleukin (IL)-6, IL-9, and IL-17A; monocyte chemoattractant protein (MCP)-1; macrophage inflammatory protein (MIP)-1; MIP-1; and Chemokine (C-C motif) ligand 5 (RANTES). The inhibitory effects of shikonin on IL-9, MIP-1, and RANTES expression were stronger than those of dexamethasone. Therefore, Shikonin can be considered a promising drug for AD treatment because it inhibits different inflammatory cytokines expression.

摘要

特应性皮炎(AD)是一种常见的炎症性皮肤病。紫草素是提取物的活性成分,具有抗炎作用。本研究的目的是探讨紫草素对AD患者促炎细胞因子和趋化因子的影响。本研究招募了10名对屋尘螨(HDM)过敏的AD患者和7名健康对照者。分离外周血单个核细胞,进一步选择CD14细胞并将其分化为树突状细胞。用主要的HDM变应原Der p 2刺激树突状细胞,与紫草素共同处理24小时,地塞米松用作对照。收集培养上清液,使用多重检测系统分析促炎细胞因子和趋化因子浓度。紫草素显著抑制Der p 2诱导的白细胞介素(IL)-6、IL-9和IL-17A、单核细胞趋化蛋白(MCP)-1、巨噬细胞炎性蛋白(MIP)-1、MIP-1以及趋化因子(C-C基序)配体5(RANTES)的表达。紫草素对IL-9、MIP-1和RANTES表达的抑制作用强于地塞米松。因此,紫草素可被认为是一种有前景的AD治疗药物,因为它能抑制不同炎症细胞因子的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a494/7417924/e42f16b0dab2/ECAM2020-9506363.001.jpg

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