Hu Zhi-Qin, Xie Shu-Shu, Zhou Ming-Yuan, Chen Yu-Chi, Zhou Fang-Mei, Ding Zhi-Shan, Ye Xiao-Qing
School of Medical Technology and Information Engineering, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Front Pharmacol. 2025 Mar 26;16:1573135. doi: 10.3389/fphar.2025.1573135. eCollection 2025.
This study aims to extract polysaccharides from Buch.-Ham. (SSP) using alcohol and water extraction and investigate whether they can be delivered orally to treat atopic dermatitis (AD). investigations demonstrated that SSP notably improved inflammation in mice, reducing ear swelling, scratching frequency, mast cell infiltration, and epidermal thickness. Furthermore, it lowered the levels of associated inflammatory markers, increased the production of skin barrier-associated proteins, and restored gut microbial diversity, which altered the composition of bacterial communities. experiments demonstrated that SSP could diminish the levels of inflammatory factors in the human immortal keratinocyte line (HaCaT) and suppress the MAPK/NF-κB signaling pathway. Our results suggest SSP exerts anti-AD effects and regulates the gut-skin axis in mice. The anti-inflammatory mechanism involves the MAPK/NF-κB signaling pathway. It is being tested for development into an effective drug for AD.
本研究旨在采用乙醇和水提取法从布氏(SSP)中提取多糖,并研究其是否可口服用于治疗特应性皮炎(AD)。研究表明,SSP显著改善了小鼠的炎症,减少了耳部肿胀、抓挠频率、肥大细胞浸润和表皮厚度。此外,它降低了相关炎症标志物的水平,增加了皮肤屏障相关蛋白的产生,并恢复了肠道微生物多样性,从而改变了细菌群落的组成。实验表明,SSP可降低人永生化角质形成细胞系(HaCaT)中炎症因子的水平,并抑制MAPK/NF-κB信号通路。我们的结果表明,SSP在小鼠中发挥抗AD作用并调节肠-皮肤轴。其抗炎机制涉及MAPK/NF-κB信号通路。目前正在对其进行测试,以开发成为一种有效的AD药物。