Rosemary essential oil microemulsion prevents DSS-induced intestinal injury in mice by modulating IL-17 signaling pathway

被引:5
|
作者
Wang, Jie [1 ,3 ]
Jia, Yanzhuo [2 ]
Xia, Ning [1 ,3 ]
Wang, Xuan [1 ,3 ]
Zhou, Peijie [1 ,3 ]
Duan, Jiawei [1 ,3 ]
Li, Jinkai [1 ,3 ]
Li, Tiaotiao [1 ,3 ]
Tang, Tiantian [1 ,3 ]
Wang, Yujiao [1 ,3 ]
Liu, Ding [1 ,3 ]
Shi, Huanxian [1 ]
Xie, Yundong [1 ]
Zhao, Chongbo [1 ,3 ]
Sun, Jing [1 ,3 ]
Zhang, Xiaofei [1 ,3 ]
机构
[1] Shaanxi Univ Chinese Med, Key Lab Basic & New Drug Res Chinese Med, Xianyang 712046, Shaanxi, Peoples R China
[2] Changan Rd Community Hlth Ctr, Xian 710000, Shaanxi, Peoples R China
[3] Shaanxi Univ Chinese Med, Shaanxi Prov Univ Engn Res Ctr, Chinese Med Aromat Ind, Xianyang 712046, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Rosemary essential oil microemulsion; Ulcerative colitis; Mechanisms of action; Transcriptomics; IL-17 signaling pathway; KAPPA-B; BIOAVAILABILITY; INFLAMMATION; ACTIVATION; TNF;
D O I
10.1016/j.jff.2024.106180
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Rosemary (Rosmarinus officinalis L) is a medicinal and edible plant. Rosemary essential oil (REO) is the principal constituent of rosemary and possesses anti-inflammatory and antioxidant properties. In this study, we evaluated the cell viability and anti-inflammatory activity of REO through the MTT assay and LPS-induced NO production in mouse RAW264.7 cells, respectively. The optimal formulation for the preparation of REO- microemulsion (REO-ME) was determined employing reversed-phase emulsification in conjunction with pseudo-triphasic diagrams. Transcriptomics, combined with network pharmacology, was employed to identify key signaling pathways, and molecular docking analysis was performed to investigate the relationship between the active ingredients of REO-ME and the key targets. The results showed that REO-ME is an O/W type ME. In addition, further pharmacodynamic experiments showed that REO-ME inhibits the expression of inflammatory factors such as IL-6, IL-1 beta, and TNF-alpha by regulating the key targets in the IL-17 signaling pathway, thereby to alleviating UC.
引用
收藏
页数:13
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