Planta Med 2019; 85(03): 210-216
DOI: 10.1055/a-0725-8334
Biological and Pharmacological Activity
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

2,6-Dimethoxy-1,4-benzoquinone Inhibits 3T3-L1 Adipocyte Differentiation via Regulation of AMPK and mTORC1

Authors

  • Hyo Jeong Son*

    1   Research Group of Natural Materials and Metabolism, Korea Food Research Institute, Wanju-gun, Republic of Korea
  • Young Jin Jang*

    1   Research Group of Natural Materials and Metabolism, Korea Food Research Institute, Wanju-gun, Republic of Korea
  • Chang Hwa Jung

    1   Research Group of Natural Materials and Metabolism, Korea Food Research Institute, Wanju-gun, Republic of Korea
    2   Division of Food Biotechnology, University of Science and Technology, Daejeon, Republic of Korea
  • Jiyun Ahn

    1   Research Group of Natural Materials and Metabolism, Korea Food Research Institute, Wanju-gun, Republic of Korea
    2   Division of Food Biotechnology, University of Science and Technology, Daejeon, Republic of Korea
  • Tae Youl Ha

    1   Research Group of Natural Materials and Metabolism, Korea Food Research Institute, Wanju-gun, Republic of Korea
    2   Division of Food Biotechnology, University of Science and Technology, Daejeon, Republic of Korea
Further Information

Publication History

received 15 May 2018
revised 16 August 2018

accepted 21 August 2018

Publication Date:
10 September 2018 (online)

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Abstract

2,6-Dimethoxy-1,4-benzoquinone is a natural phytochemical present in fermented wheat germ. It has been reported to exhibit anti-inflammatory, antitumor, and antibacterial activities. However, the anti-adipogenic effects of 2,6-dimethoxy-1,4-benzoquinone and the mechanisms responsible have not previously been elucidated. Such findings may have ramifications for the treatment of obesity. 2,6-Dimethoxy-1,4-benzoquinone (5 and 7.5 µM) significantly reduced the expression of various adipogenic transcription factors, including peroxisome proliferator-activated receptor-γ and CCAAT/enhancer binding protein α as well as adipocyte protein 2 and fatty acid synthase. 2,6-Dimethoxy-1,4-benzoquinone upregulated AMP-dependent protein kinase phosphorylation and inhibited the mature form of sterol regulatory element-binding protein 1c. Notably, 2,6-dimethoxy-1,4-benzoquinone attenuated mammalian target of rapamycin complex 1 activity in 3T3-L1 and mouse embryonic fibroblast cells. These findings highlight a potential role for 2,6-dimethoxy-1,4-benzoquinone in the suppression of adipogenesis. Further studies to determine the anti-obesity effects of 2,6-dimethoxy-1,4-benzoquinone in animal models appear warranted.

* These authors contributed equally to this work.