Leaf Extract of Perilla frutescens (L.) Britt Promotes Adipocyte Browning via the p38 MAPK Pathway and PI3K-AKT Pathway

被引:0
|
作者
Chen, Fancheng [1 ,2 ]
Wu, Silin [3 ]
Li, Dejian [4 ]
Dong, Jian [1 ]
Huang, Xiaowei [5 ,6 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Orthoped Surg, Shanghai 200032, Peoples R China
[2] Yale Univ, Sch Med, Dept Orthopaed & Rehabil, New Haven, CT 06510 USA
[3] Univ Texas Hlth Sci Ctr, McGovern Sch Med, Dept Neurosurg, Houston, TX 77030 USA
[4] Fudan Univ Pudong Med Ctr, Shanghai Pudong Hosp, Dept Orthoped, Shanghai 200120, Peoples R China
[5] Eberhard Karls Univ Tubingen, Fac Med, D-72076 Tubingen, Germany
[6] Soochow Univ, Affiliated Hosp 1, Dept Orthopaed, Suzhou 215006, Peoples R China
基金
中国国家自然科学基金;
关键词
Perilla frutescens (L; ) Britt; network pharmacology; adipocyte browning; in vitro validation; molecular mechanism; OBESITY; ACCURACY; ASTHMA;
D O I
10.3390/nu15061487
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The leaf of Perilla frutescens (L.) Britt (PF) has been reported to negatively affect adipocyte formation, inhibit body-fat formation, and lower body weight. However, its effect on adipocyte browning remains unknown. Thus, the mechanism of PF in promoting adipocyte browning was investigated. The ingredients of PF were acquired from the online database and filtered with oral bioavailability and drug-likeness criteria. The browning-related target genes were obtained from the Gene Card database. A Venn diagram was employed to obtain the overlapped genes that may play a part in PF promoting adipocyte browning, and an enrichment was analysis conducted based on these overlapped genes. A total of 17 active ingredients of PF were filtered, which may regulate intracellular receptor-signaling pathways, the activation of protein kinase activity, and other pathways through 56 targets. In vitro validation showed that PF promotes mitochondrial biogenesis and upregulates brite adipocyte-related gene expression. The browning effect of PF can be mediated by the p38 MAPK pathway as well as PI3K-AKT pathway. The study revealed that PF could promote adipocyte browning through multitargets and multipathways. An in vitro study validated that the browning effect of PF can be mediated by both the P38 MAPK pathway and the PI3K-AKT pathway.
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页数:24
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