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龙血竭活性成分对紫外线B诱导皮肤损伤的抗炎及屏障修复机制

Anti-inflammatory and barrier repair mechanisms of active components in Daemonorops draco Bl. for UVB-induced skin damage.

作者信息

Wu Xingyi, Zhang Ying, Yi Fan, Geng Zaijun, Guo Miaomiao, Ling Xiao, Li Jun, Li Li

机构信息

Beijing Key Lab of Plant Resource Research and Development, Beijing Technology and Business University, Fucheng Road, Haidian District, Beijing, 100048, China.

Beijing Lan Divine Technology Co. LTD, Culture Building, No. A59, Zhongguancun Street, Haidian District, Beijing, 100872, China.

出版信息

Sci Rep. 2025 May 17;15(1):17124. doi: 10.1038/s41598-025-01289-4.

Abstract

Daemonorops draco Bl. extract and its active ingredients can remove blood stasis and promote muscle and wound healing and are widely used in skin health and other fields. Modern pharmacological studies have demonstrated that this extract exerts excellent anti-inflammatory effects beneficial for skin barrier repair. However, the mechanism of action and monomeric components of D. draco remain unclear. Seven active monomers (XJ-1 ~ XJ-7) were extracted and purified from D. draco. The successful construction of the HaCaT inflammation model was achieved through the detection of IL-1β and TNF-α expressions in UVB-irradiated HaCaT cells. Based on this cellular model, (2 S)-5-methoxy-6-methylflavan-7-ol (XJ-2) was determined to be the best-screened monomer. The effects of XJ-2 on the production of reactive oxygen species (ROS) and Ca in HaCaT cells were investigated using fluorescent probes and flow cytometry, respectively. The impact of XJ-2 on the expression of crucial proteins within the NF-κB pathway was examined via immunofluorescence and western blotting. The expression levels of downstream inflammatory factors, namely IL-1β and TNF-α, were detected through PCR. The effects of XJ-2 on the expression of skin barrier-related factors filaggrin (FLG), aquaporin 3 (AQP-3), and claudin1 (CLDN1) were investigated using PCR, immunofluorescence, and western blotting. Based on these findings, we comprehensively examined the mechanisms underlying the anti-inflammatory and barrier repair effects of XJ-2. XJ-2 primarily protected the internal structure and function of the cells by inhibiting the mass production of ROS and Ca inflow. XJ-2 exerts anti-inflammatory effects by regulating the key proteins of the NF-κB/IKKα pathway and reducing the expression of inflammatory factors. XJ-2 repairs skin barrier damage by regulating multiple factors. Compound XJ-2 from D. draco exerts excellent anti-inflammatory and barrier repair effects, possesses great potential for the treatment of skin diseases, and can be used as a dermatological drug to repair skin barrier damage.

摘要

血竭提取物及其活性成分具有活血化瘀、促进肌肉和伤口愈合的作用,广泛应用于皮肤健康等领域。现代药理研究表明,该提取物具有良好的抗炎作用,有利于皮肤屏障修复。然而,血竭的作用机制和单体成分尚不清楚。从血竭中提取并纯化出7种活性单体(XJ-1~XJ-7)。通过检测紫外线B(UVB)照射的人永生化角质形成细胞(HaCaT细胞)中白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的表达,成功构建了HaCaT炎症模型。基于该细胞模型,确定(2S)-5-甲氧基-6-甲基黄烷-7-醇(XJ-2)为筛选出的最佳单体。分别使用荧光探针和流式细胞术研究了XJ-2对HaCaT细胞中活性氧(ROS)产生和钙离子(Ca)的影响。通过免疫荧光和蛋白质免疫印迹法检测XJ-2对核因子-κB(NF-κB)通路关键蛋白表达的影响。通过聚合酶链反应(PCR)检测下游炎症因子IL-1β和TNF-α的表达水平。使用PCR、免疫荧光和蛋白质免疫印迹法研究了XJ-2对皮肤屏障相关因子丝聚蛋白(FLG)、水通道蛋白3(AQP-3)和紧密连接蛋白1(CLDN1)表达的影响。基于这些发现,我们全面研究了XJ-2抗炎和屏障修复作用的潜在机制。XJ-2主要通过抑制ROS的大量产生和Ca内流来保护细胞的内部结构和功能。XJ-2通过调节NF-κB/IKKα通路的关键蛋白并降低炎症因子的表达发挥抗炎作用。XJ-2通过调节多种因子修复皮肤屏障损伤。血竭中的化合物XJ-2具有良好的抗炎和屏障修复作用,在皮肤病治疗方面具有巨大潜力,可作为修复皮肤屏障损伤的皮肤科药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a2/12085626/f8172ed3e0d9/41598_2025_1289_Fig1_HTML.jpg

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