基化Smilax glabra粉通过肠-皮肤轴调节通过结肠向的输送来缓解亚托邦性皮炎
Nan Wang1, Lingling Wu1, Yaya Su1
1Department of Pharmacy, Air Force Medical Center, PLA, Air Force Medical University, Beijing 100142, China.
Acta pharmaceutica Sinica. B
|January 1, 2026
概括
丁化Smilax glabra粉 (BSGS) 通过在结肠中释放丁酸盐,有效治疗亚托皮炎 (AD). 这种新的方法调节肠-皮肤轴,减少炎症并改善潜在的AD治疗的肠道健康.
科学领域:
- 微生物学 微生物学
- 免疫学 免疫学 免疫学
- 胃肠病学 胃肠病学
背景情况:
- 亚托邦性皮肤炎 (AD) 是一种广泛的炎症性皮肤疾病,具有免疫失调.
- 丁酸盐是一种来自肠道微生物群的短链脂肪酸,显示出对AD有益的抗炎性质.
- 针对阿尔茨海默病的治疗,向结肠注入酸的向治疗方法仍未得到充分研究.
研究的目的:
- 合成基化Smilax glabra粉 (BSGS) 用于结肠特异性酸盐释放.
- 通过调节肠-皮肤轴来研究BSGS对亚托皮炎 (AD) 的治疗疗效.
主要方法:
- BSGS的合成和特征是其晶体结构和抵抗消化的能力.
- 试管发酵评估了BSGS生产短链脂肪酸和影响微生物组成的能力.
- 用AD小鼠模型来评估BSGS对皮肤炎症,细胞因子水平,肠道屏障和肠道微生物群的影响.
主要成果:
- 在发酵过程中,BSGS对胃肠道消化表现出耐药性,并促进了酸盐的产生.
- 在AD小鼠中施用BSGS可降低皮肤炎症,降低血清前炎性细胞因子,并改善肠道屏障功能.
- BSGS调节了肠道微生物组成,并抑制了NF-κB炎症途径.
结论:
- BSGS作为一种针对结肠的新甲基酸盐供体,具有针对亚托皮炎的显著治疗潜力.
- 通过酸盐释放调节肠皮轴和免疫反应是BSGS疗效的关键机制.
- 通过准肠道微生物群和炎症,BSGS提供了一种有希望的AD管理策略.
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