Network pharmacology-based research uncovers cold resistance and thermogenesis mechanism of Cinnamomum cassia

被引:14
|
作者
Xiang-Li [1 ,2 ]
Bo-Xing [1 ]
Xin-Liu [1 ]
Jiang, Xiao-wen [1 ]
Lu, Hong-yuan [1 ]
Xu, Zi-Hua [1 ]
Yue-Yang [1 ]
Qiong-Wu [1 ]
Dong-Yao [2 ]
Zhang, Ying-Shi [1 ]
Zhao, Qing-Chun [1 ,2 ]
机构
[1] Shenyang Pharmaceut Univ, Dept Life Sci & Biochem, Shenyang 110016, Peoples R China
[2] Gen Hosp Northern Theater Command, Dept Pharm, Shenyang 110840, Peoples R China
关键词
Network pharmacology; Cinnamon; Thermogenesis; ACTIVATED RECEPTOR-ALPHA; CHINESE HERBAL MEDICINE; BROWN ADIPOSE-TISSUE; INTEGRATING INFORMATION; ENERGY-METABOLISM; PLASMA-GLUCOSE; DIFFERENTIATION; PROTEIN; CINNAMALDEHYDE; EXPRESSION;
D O I
10.1016/j.fitote.2020.104824
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Cinnamomum cassia (L.) J.Presl (Cinnamon) was known as a kind of hot herb, improved circulation and warmed the body. However, the active components and mechanisms of dispelling cold remain unknown. Methods: The effects of several Chinses herbs on thermogenesis were evaluated on body temperature and activation of brown adipose tissue. After confirming the effect, the components of cinnamon were identified using HPLC-Q-TOF/MS and screened with databases. The targets of components were obtained with TCMSP, SymMap, Swiss and STITCH databases. Thermogenesis genes were predicted with DisGeNET and GeneCards databases. The protein-protein interaction network was constructed with Cytoscape 3.7.1 software. GO enrichment analysis was accomplished with STRING databases. KEGG pathway analysis was established with Omicshare tools. The top 20 targets for four compounds were obtained according to the number of edges of PPI network. In addition, the network results were verified with experimental research for the effects of extracts and major compounds. Results: Cinnamon extract significantly upregulated the body temperature during cold exposure.121 components were identified in HPLC-Q-TOF/MS. Among them, 60 compounds were included in the databases. 116 targets were obtained for the compounds, and 41 genes were related to thermogenesis. The network results revealed that 27 active ingredients and 39 target genes. Through the KEGG analysis, the top 3 pathways were PPAR signaling pathway, AMPK signaling pathway, thermogenesis pathway. The thermogenic protein PPAR gamma, UCP1 and PGC1-alpha was included in the critical targets of four major compounds. The three major compounds increased the lipid consumption and activated the brown adipocyte. They also upregulated the expression of UCP1, PGC1-alpha and pHSL, especially 2-methoxycinnamaldehyde was confirmed the effect for the first time. Furthermore, cinnamaldehyde and cinnamon extract activated the expression of TRPA1 on DRG cells. Conclusion: The mechanisms of cinnamon on cold resistance were investigated with network pharmacology and experiment validation. This work provided research direction to support the traditional applications of thermogenesis.
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页数:15
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