1. Academic Validation
  2. Ginsenoside Rb1 Facilitates Browning by Repressing Wnt/β-Catenin Signaling in 3T3-L1 Adipocytes

Ginsenoside Rb1 Facilitates Browning by Repressing Wnt/β-Catenin Signaling in 3T3-L1 Adipocytes

  • Med Sci Monit. 2021 Jan 27;27:e928619. doi: 10.12659/MSM.928619.
Qingxin Fan 1 2 Pengjiao Xi 3 Derun Tian 1 3 Lianqun Jia 4 Yuan Cao 4 Kaixuan Zhan 4 Tianwei Sun 5 Yinlong Zhang 6 Qiming Wang 1 4
Affiliations

Affiliations

  • 1 Department of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China (mainland).
  • 2 Hospital of Chengdu Office of People's Government of Tibetan Autonomous Region (Hospital C. T.), Chengdu, Sichuan, China (mainland).
  • 3 School of Medical Laboratory, Tianjin Medical University, Tianjin, China (mainland).
  • 4 Key Laboratory of Ministry of Education for TCM Viscera-State Theory and Applications, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, China (mainland).
  • 5 Department of Spinal Surgery, Tianjin People's Hospital, Tianjin, China (mainland).
  • 6 Department of Orthopedic Trauma, Tianjin People's Hospital, Tianjin, China (mainland).
Abstract

BACKGROUND The discovery of browning in white adipose tissue has provided new ideas for treating obesity. Many studies have reported that ginsenoside Rb1 (G-Rb1) has activity against diabetes, inflammation, and obesity, but further investigation is needed on the effect and mechanism of G-Rb1 on browning. MATERIAL AND METHODS We treated 3T3-L1 adipocytes with 0-200 μM G-Rb1, and 0.5 μM Compound 3f and 30 μM SKL2001 were used to activate Wnt/b-catenin signaling. Adipocyte activity was evaluated by Cell Counting Kit-8. Oil Red O staining was used to detect the lipid droplets. Quantitative real-time polymerase chain reaction was used to measure the expression of Cd-137, Cited-1, Txb-1, Prdm-16, and Ucp-1 mRNA. Western blotting was used to measure the expression of Ucp-1, pGSK-3ß (Ser 9), GSK- 3ß, and ß-catenin proteins. The expression of Ucp-1 was also detected with immunofluorescence. RESULTS Adipocyte activity was not affected by 0-100 μM G-Rb1. However, G-Rb1 dose-dependently reduced the accumulation of lipid droplets; increased the expression of Cd-137, Cited-1, Txb-1, Prdm-16, and Ucp-1 mRNA; and increased the expression of Ucp-1, pGSK-3ß (Ser 9), GSK-3ß, and ß-catenin proteins. The accumulation of lipid droplets and the expression of Ucp-1 protein decreased as b-catenin increased. CONCLUSIONS G-Rb1 at various concentrations (0-100 μM) promoted the browning of adipocytes in a dose-dependent manner. Further, we confirmed that activation of Wnt/ß-catenin signaling could inhibit browning. Therefore, the browning promoted by G-Rb1 may be associated with the inhibition of Wnt/ß-catenin signaling.

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