Therapeutic Effect and Mechanism of Glabridin Liposome on Imiquimod-induced Mice Psoriasis

被引:4
作者
Lu, Yongjie [1 ]
Cheng, Lushi [1 ]
Ren, Lu [1 ]
Chen, Dongqiu [1 ]
Guan, Shumin [1 ]
Zhu, Siyang [1 ]
Xu, Xian [1 ]
Zhang, Bing [2 ]
Tang, Minghui [1 ]
Zhang, Chijian [1 ]
Ai, Yong [1 ]
Zhang, Lanyue [3 ,4 ]
He, Tinggang [1 ]
机构
[1] Hua An Tang Biotech Grp Co Ltd, Guangzhou, Peoples R China
[2] Guangdong He Ji Biotech Co Ltd, Guangzhou, Peoples R China
[3] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, Guangzhou, Peoples R China
[4] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, Guangzhou 510006, Peoples R China
关键词
Glabridin liposome; psoriasis; anti-inflammatory; imiquimod; skin tissue; ESSENTIAL OILS; SKIN; INFLAMMATION;
D O I
10.1177/09731296231198931
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Glabridin is one of the main components of the isoflavonoids in Glycyrrhiza glabra and possesses anti-inflammatory, antibacterial, and anticancer effects. Objectives: Herein, the therapeutic effects and mechanisms of action of the glabridin liposome (GL) complex were studied in mice with imiquimod-induced psoriasis. Materials and Methods: After treatment with GLs, their effectiveness was assessed using parameters, such as Psoriasis Area and Severity Index (PASI) score, histopathology, inflammatory cytokines, and psoriasis-associated proteins. Results: The results demonstrated that GLs could significantly improve psoriatic symptoms, downregulate mast cell infiltration, and significantly reduce the PASI score of psoriatic mice. Quantitative reverse transcription polymerase chain reaction (RT-qPCR) results showed that GLs significantly decreased IL-23 and STAT3 mRNA expression. The results of immunohistochemistry and the enzyme-linked immunosorbent assay indicated that GLs decreased the expression of tumor necrosis factor-alpha (TNF-alpha), IL-17, and IL-22. Conclusion: GLs can alleviate psoriasis by inhibiting the expression of keratinocyte-activating proteins. These results suggest that GLs have great potential for the clinical treatment of psoriasis.
引用
收藏
页码:72 / 80
页数:9
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