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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Indirubin, a purple 3,2-bisindole, inhibited allergic contact dermatitis via regulating T helper (Th)-mediated immune system in DNCB-induced model
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Indirubin, a purple 3,2-bisindole, inhibited allergic contact dermatitis via regulating T helper (Th)-mediated immune system in DNCB-induced model

机译:紫色3,2-双吲哚靛玉红通过调节DNCB诱导的模型中T辅助介导的免疫系统抑制过敏性接触性皮炎

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Ethnopharmacological relevance: Indirubin, isolated from Indigo naturalis (Apiaceae) is a purple 3,2- bisindole and a stable isomer of indigo. Although it is known to have anti-inflammatory activities, its mechanism of action has not been elucidated. Materials and methods: Seven-week-old female BALB/c mice were sensitized with 1-chloro-2,4-dinitrobenzene (DNCB) to induce skin inflammation. Hematoxylin and eosin staining was performed to assess epidermal and dermal hyperplasia, which were determined by measuring the thicknesses of the epidermis and dermis, respectively. We also evaluated serum immunoglobulin E (IgE) levels and cytokines production, such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-4, 6 and Interferon (IFN)-gamma. In addition, we investigated nuclear factor (NF)-κB, IκB-α and mitogen-activated protein (MAP) kinase activities for verifying the molecular mechanism of inflammation. Results: Indirubin treatment suppressed skin inflammation in DNCB-exposed mice. The skin lesions were significantly thinner in the Indirubin-treated group than in untreated controls, and the hyperkeratosis disappeared. Indirubin reduced the total serum IgE level and cytokines production. In addition, it normalized NF-κB, IκB-α and MAP kinase expression. Conclusions: Indirubin might be a useful treatment for allergic contact dermatitis via regulating the co-expression of T helper (Th) 1 and 2 cell-mediated immune responses.
机译:人类药理学相关性:从自然靛蓝(Apiaceae)中分离出来的靛玉红是紫色的3,2-双吲哚和靛蓝的稳定异构体。尽管已知它具有抗炎活性,但其作用机理尚未阐明。材料和方法:用1-氯-2,4-二硝基苯(DNCB)使七周大的雌性BALB / c小鼠致敏,以引起皮肤炎症。进行苏木精和曙红染色以评估表皮和真皮增生,这分别通过测量表皮和真皮的厚度来确定。我们还评估了血清免疫球蛋白E(IgE)的水平和细胞因子的产生,例如肿瘤坏死因子(TNF)-α,白介素(IL)-4、6和干扰素(IFN)-γ。此外,我们调查了核因子(NF)-κB,IκB-α和有丝分裂原活化蛋白(MAP)激酶活性,以验证炎症的分子机制。结果:靛玉红治疗抑制了DNCB暴露小鼠的皮肤炎症。靛红素治疗组的皮肤病变明显较未治疗的对照组更薄,并且过度角化消失。靛玉红降低了血清总IgE水平和细胞因子的产生。此外,它使NF-κB,IκB-α和MAP激酶表达正常化。结论:靛玉红可能通过调节T辅助细胞(Th)1和2介导的免疫应答的共表达来治疗过敏性接触性皮炎。

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