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Synthesis of a new [6]-gingerol analogue and its protective effect with respect to the development of metabolic syndrome in mice fed a high-fat diet

Research Project

Project/Area Number 26870647
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Biomolecular chemistry
Chemical biology
Research InstitutionNational Center for Global Health and Medicine (2016)
Waseda University (2014-2015)

Principal Investigator

OKAMOTO MAYUMI  国立研究開発法人国立国際医療研究センター, その他部局等, 上級研究員 (40533104)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsショウガ / 体重増加抑制 / 血糖 / ジンゲロール / [6]-gingerol / アフィニティ磁性ビーズ / 褐色脂肪 / メタボリック症候群 / 脂肪細胞
Outline of Final Research Achievements

To determine the effects of a [6]-gingerol analogue (6G), a major chemical component of the ginger rhizome, and its stable analogue after digestion in simulated gastric fluid, aza-[6]-gingerol (A6G), on diet-induced body fat accumulation, we synthesized 6G and A6G. Mice were fed either a control regular rodent chow, a high-fat diet (HFD), or a HFD supplemented with 6G and A6G. Supplementation with 6G and A6G significantly reduced body weight gain, fat accumulation, and circulating levels of insulin and leptin. The mRNA levels of sterol regulatory element-binding protein 1c (SREBP-1c) and acetyl-CoA carboxylase 1 in the liver were significantly lower in mice fed A6G than in HFD control mice. Our findings indicate that A6G, rather than 6G, enhances energy metabolism and reduces the extent of lipogenesis by downregulating SREBP-1c and its related molecules, which leads to the suppression of body fat accumulation.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (7 results)

All 2017 2016 2015 Other

All Int'l Joint Research (1 results) Journal Article (4 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 4 results,  Open Access: 1 results,  Acknowledgement Compliant: 2 results) Presentation (2 results) (of which Int'l Joint Research: 2 results)

  • [Int'l Joint Research] A*STAR(Singapore)

    • Related Report
      2015 Research-status Report
  • [Journal Article] Synthesis and basic evaluation of 7α-(3-[18F]fluoropropyl)-testosterone and 7α-(3-[18F]fluoropropyl)-dihydrotestosterone.2017

    • Author(s)
      Okamoto M, Naka K, Ishiwata K, Shimizu I, Toyohara J
    • Journal Title

      Ann. Nucl. Med

      Volume: 31 Issue: 1 Pages: 53-62

    • DOI

      10.1007/s12149-016-1130-7

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Optimization of the alkyl side chain length of fluorine-18-labeled 7α-alkyl-fluoroestradiol.2016

    • Author(s)
      Okamoto M, Shibayama H, Naka K, Kitagawa Y, Ishiwata K, Shimizu I, Toyohara J.
    • Journal Title

      Nucl. Med. Biol.

      Volume: 43 Issue: 8 Pages: 512-519

    • DOI

      10.1016/j.nucmedbio.2016.05.008

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] (R)-[11C]Emopamil as a novel tracer for imaging enhanced P-glycoprotein function. (R)-[11C]Emopamil as a novel tracer for imaging enhanced P-glycoprotein function.2016

    • Author(s)
      Jun Toyohara, Mayumi Okamoto, Hiroki Aramaki, Yuto Zaitsu, Isao Shimizu, Kiichi Ishiwata.
    • Journal Title

      Nuclear Medicine and Biology

      Volume: 43 Issue: 1 Pages: 52-63

    • DOI

      10.1016/j.nucmedbio.2015.09.001

    • Related Report
      2016 Annual Research Report 2015 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Synthesis and evaluation of 7α-(3-[18F]fluoropropyl) estradiol.2015

    • Author(s)
      2.Mayumi Okamoto, Kyosuke Naka, Yuya Kitagawa, Kiichi Ishiwata, Mitsuyoshi Yoshimoto, Isao Shimizu, Jun Toyohara.
    • Journal Title

      Nuclear Medicine and Biology

      Volume: 42 Issue: 7 Pages: 590-597

    • DOI

      10.1016/j.nucmedbio.2015.03.005

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Int'l Joint Research
  • [Presentation] “Radiosynthesis and fundamental evaluation of (R)-[11C]emopamil as a novel tracer for imaging enhanced P- glycoprotein function in the brain ”2015

    • Author(s)
      Jun Toyohara, Mayumi Okamoto, Hiroki Aramaki, Yuto Zaitsu, Isao Shimizu, Seijiro Hosokawa, Kiichi Ishiwata.
    • Organizer
      Annual Congress of the European Association of Nuclear Medicine
    • Place of Presentation
      Humburg, Germany
    • Year and Date
      2015-10-10
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] “Structure activity relationships of 18F-labeled 7α-alkyl-estradiol derivatives”2015

    • Author(s)
      Jun Toyohara, Mayumi Okamoto, Hiromitsu Shibayama, Kyosuke Naka, Yuya Kitagawa, Kiichi Ishiwata, Isao Shimizu.
    • Organizer
      The 21th International Symposium on Radiopharmaceutical Sciences
    • Place of Presentation
      Missouri, USA
    • Year and Date
      2015-05-26
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research

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Published: 2014-04-04   Modified: 2018-03-22  

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