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

Author:

Chen Fancheng12,Wu Silin3,Li Dejian4,Dong Jian1,Huang Xiaowei56

Affiliation:

1. Department of Orthopedic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China

2. Department of Orthopaedics & Rehabilitation, School of Medicine, Yale University, New Haven, CT 06510, USA

3. Department of Neurosurgery, McGovern School of Medicine, University of Texas Health Science Center, Houston, TX 77030, USA

4. Department of Orthopedics, Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai 200120, China

5. Facutly of Medicine, Eberhard Karls University of Tübingen, 72076 Tübingen, Germany

6. Department of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou 215006, China

Abstract

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.

Funder

National Natural Science Foundation of China

Talents Training Program of Pudong Hospital affiliated to Fudan University

Scientific Research Foundation provided by Pudong Hospital affiliated to Fudan University

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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