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Ribes fasciculatum var. chinense Attenuated Allergic Inflammation In Vivo and In Vitro

机译:筋膜肋骨变种。 chinense减轻了体内和体外的过敏性炎症

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摘要

Ribes fasciculatum var. chinense MAX. (R. fasciculatum) has traditionally been used in Korea to treat inflammatory diseases. However, the exact mechanism that accounts for the anti-inflammatory effect of R. fasciculatum is not completely understood. We aimed to ascertain the pharmacological effects of R. fasciculatum on both compound 48/80- or histamine-induced scratching behaviors and 2, 4-dinitrochlorobenzene (DNCB)-induced atopic dermatitis (AD) in mice. Additionally, to find a possible explanation for the anti-inflammatory effects of R. fasciculatum, we evaluated the effects of R. fasciculatum on the production of inflammatory mediators in LPS-stimulated macrophage cells. Treatment of R. fasciculatum significantly reduced compound 48/80- or histamine-induced the pruritus in mice. R. fasciculatum attenuated the AD symptoms such as eczematous, erythema and dryness and serum IgE levels in AD model. Additionally, R. fasciculatum inhibited the production of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6). The maximal rates of TNF-α and IL-6 inhibition by R. fasciculatum (1 mg/ml) were approximately 32.12% and 46.24%, respectively. We also showed that R. fasciculatum inhibited the activation of nuclear factor-kappa B in LPS-stimulated macrophages. Collectively, the findings of this study provide us with novel insights into the pharmacological actions of R. fasciculatum as a potential molecule for use in the treatment of allergic inflammatory diseases.
机译:筋膜肋骨变种。中国最大(R. fasciculatum)在韩国传统上用于治疗炎性疾病。但是,尚不完全了解导致Fasciculatum抗炎作用的确切机制。我们旨在确定fasciculatum对化合物48/80或组胺诱导的scratch抓行为和2,4-二硝基氯苯(DNCB)诱导的特应性皮炎(AD)的药理作用。另外,为了找到对筋膜盘根霉的抗炎作用的可能解释,我们评估了筋膜盘根霉对LPS刺激的巨噬细胞中炎性介质产生的影响。 Fasciculatum的治疗显着降低了化合物48/80或组胺诱导的小鼠瘙痒症。 Fasciculatum减轻了AD模型中的AD症状,例如湿疹,红斑和干燥以及血清IgE水平。另外,fasciculatum抑制了肿瘤坏死因子-α(TNF-α)和白介素6(IL-6)的产生。 Fasciculatum(1 mg / ml)对TNF-α和IL-6的最大抑制率分别约为32.12%和46.24%。我们还表明,fasciculatum R. fasciculatum抑制了LPS刺激的巨噬细胞中核因子kappa B的激活。总的来说,这项研究的发现为我们提供了关于fasciculatum R. fasciculatum作为治疗过敏性炎症性疾病的潜在分子的药理作用的新见解。

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