Department of Pharmacological and Molecular Sciences, University of Milan, 20133 Milan, Italy.
Specialist in Dermatology and Venereology, Corso di Porta Romana 131, 20122 Milan, Italy.
Molecules. 2021 May 20;26(10):3044. doi: 10.3390/molecules26103044.
L. (blackcurrant) leaf extracts, due to high levels of flavonols and anthocyanins, have been shown to exhibit beneficial effects in inflammatory diseases. However, whereas their traditional use has been investigated and validated in several models of inflammation and oxidative stress, the possible impact on skin disorders is still largely unknown. The purpose of this work was to elucidate the effects of leaf extract (RNLE) on keratinocyte-derived inflammatory mediators, elicited by a Th1 or Th2 cytokine milieu. HaCaT cells were challenged with TNF-α, either alone or in combination with the costimulatory cytokines IFN-γ or IL-4, and the release of proinflammatory cytokines and mediators (IL-8, IL-6, s-ICAM-1, and TSLP) was evaluated. The results showed that RNLE preferentially interferes with IFN-γ signaling, demonstrating only negligible activity on TNF-α or IL-4. This effect was attributed to flavonols, which might also account for the ability of RNLE to impair TNF-α/IL-4-induced TSLP release in a cAMP-independent manner. These results suggest that RNLE could have an antiallergic effect mediated in keratinocytes via mechanisms beyond histamine involvement. In conclusion, the discovery of RNLE preferential activity against IFN-γ-mediated inflammation suggests potential selectivity against Th1 type response and the possible use in Th1 inflammatory diseases.
黑加仑叶提取物因含有高水平的类黄酮和花青素,已被证明在炎症性疾病中具有有益作用。然而,尽管其传统用途已在多种炎症和氧化应激模型中得到研究和验证,但对皮肤疾病的潜在影响仍知之甚少。本研究旨在阐明黑加仑叶提取物(RNLE)对角质形成细胞来源的促炎介质的影响,这些介质是由 Th1 或 Th2 细胞因子环境引发的。用 TNF-α 单独或与共刺激细胞因子 IFN-γ 或 IL-4 一起挑战 HaCaT 细胞,并评估促炎细胞因子和介质(IL-8、IL-6、s-ICAM-1 和 TSLP)的释放。结果表明,RNLE 优先干扰 IFN-γ 信号,对 TNF-α 或 IL-4 的活性可忽略不计。这种作用归因于类黄酮,这也可能解释了 RNLE 以 cAMP 非依赖性方式损害 TNF-α/IL-4 诱导的 TSLP 释放的能力。这些结果表明,RNLE 可能通过超越组胺参与的机制在角质形成细胞中发挥抗过敏作用。总之,发现 RNLE 对 IFN-γ 介导的炎症具有优先活性,提示其对 Th1 型反应具有潜在的选择性,并可能用于 Th1 炎症性疾病。