Ginkgolide C Suppresses Adipogenesis in 3T3-L1 Adipocytes via the AMPK Signaling Pathway

  • Evid Based Complement Alternat Med. 2015;2015:298635. doi: 10.1155/2015/298635.
Chian-Jiun Liou  1 Xuan-Yu Lai  2 Ya-Ling Chen  3 Chia-Ling Wang  4 Ciao-Han Wei  4 Wen-Chung Huang  5
Affiliations
  • 1. Department of Nursing, Chang Gung University of Science and Technology, 261 Wen-Hwa 1st Road, Kwei-Shan, Taoyuan, Taiwan.
  • 2. Department of Nutrition and Health Sciences, Chang Gung University of Science and Technology, 261 Wen-Hwa 1st Road, Kwei-Shan, Taoyuan, Taiwan ; Graduate Institute of Health Industry Technology, Chang Gung University of Science and Technology, Kwei-Shan, Taoyuan, Taiwan.
  • 3. Department of Nutrition and Health Sciences, Chang Gung University of Science and Technology, 261 Wen-Hwa 1st Road, Kwei-Shan, Taoyuan, Taiwan.
  • 4. Graduate Institute of Health Industry Technology, Chang Gung University of Science and Technology, Kwei-Shan, Taoyuan, Taiwan.
  • 5. Graduate Institute of Health Industry Technology, Chang Gung University of Science and Technology, Kwei-Shan, Taoyuan, Taiwan ; Research Center for Industry of Human Ecology, Chang Gung University of Science and Technology, Kwei-Shan, Taoyuan, Taiwan.
Abstract

Ginkgolide C, isolated from Ginkgo biloba leaves, is a diterpene lactone derivative [corrected] reported to have multiple biological functions, from decreased platelet aggregation to ameliorating Alzheimer disease. The study aim was to evaluate the antiadipogenic effect of ginkgolide C in 3T3-L1 adipocytes. Ginkgolide C was used to treat differentiated 3T3-L1 cells. Cell supernatant was collected to assay glycerol release, and cells were lysed to measure protein and gene expression related to adipogenesis and lipolysis by western blot and Real-Time PCR, respectively. Ginkgolide C significantly suppressed lipid accumulation in differentiated adipocytes. It also decreased adipogenesis-related transcription factor expression, including Peroxisome Proliferator-activated Receptor and CCAAT/enhancer-binding protein. Furthermore, ginkgolide C enhanced adipose triglyceride Lipase and hormone-sensitive Lipase production for lipolysis and increased phosphorylation of AMP-activated protein kinase (AMPK), resulting in decreased activity of Acetyl-CoA Carboxylase for fatty acid synthesis. In coculture with an AMPK Inhibitor (compound C), ginkgolide C also improved activation of Sirtuin 1 and phosphorylation of AMPK in differentiated 3T3-L1 cells. The results suggest that ginkgolide C is an effective flavone for increasing lipolysis and inhibiting adipogenesis in adipocytes through the activated AMPK pathway.

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