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Functional roles of FGF23/alpha-Klotho system in the regulation of food intake.

Research Project

Project/Area Number 17K19924
Research Category

Grant-in-Aid for Challenging Research (Exploratory)

Allocation TypeMulti-year Fund
Research Field Health science and related fields
Research InstitutionWakayama Medical University

Principal Investigator

Komori Tadasuke  和歌山県立医科大学, 医学部, 講師 (90433359)

Project Period (FY) 2017-06-30 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥6,500,000 (Direct Cost: ¥5,000,000、Indirect Cost: ¥1,500,000)
Fiscal Year 2018: ¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2017: ¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Keywords視床下部 / FGF23 / αKlotho / 摂食調節 / hypothalamus / food intake / body temperature / 絶食 / 老化 / 運動 / FGF23/αKlothoシステム
Outline of Final Research Achievements

To investigate the functional roles of FGF23 in the hypothalamus, we injected FGF23 intracerebroventricularly into fasted mice. Intracerebroventricular injection of FGF23 induced the expression of Egr1 in the hypothalamus. In addition, amount of 2-hour food intake was increased by FGF23. FGF23 induced the gene expression of NPY and AgRP in the hypothalamus. These results suggest that FGF23 is a novel important regulator of food intake during fasting. Next, we analyzed the body temperature in αKlotho-deficient mice in both fed and fasted conditions. As homozygous αKlotho-deficient mice show severe physical abnormalities like human premature aging, we used heterozygous αKlotho-deficient (αKlotho+/-) mice. There were no differences in the body temperature between WT and αKlotho+/- mice in the fed condition. However, the fasting-induced decrease in body temperature observed in WT mice was less severe in αKlotho+/- mice.

Academic Significance and Societal Importance of the Research Achievements

健康寿命(健康上の問題で日常生活が制限されることなく生活できる期間)延伸の鍵は適切な食事と運動にあると考えられおり、食事や運動が個体の老化に及ぼす影響の分子機序が注目されている。抗老化遺伝子であるαKlothoの発見により様々な個体の老化メカニズムが明らかとなってきたが、FGF23/αKlothoシステムと摂食や運動との関連性は不明のままであった。本研究では、αKlothoとそのリガンドであるFGF23が視床下部において摂食・エネルギー代謝を制御する新たな因子である事を発見した。これらの結果は、中枢神経系を介した個体の老化メカニズムの解明へと繋がることが期待される。

Report

(3 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • Research Products

    (6 results)

All 2019 2018

All Presentation (6 results) (of which Int'l Joint Research: 3 results)

  • [Presentation] Functional roles of FGF23-αKlotho system in the regulation of food intake and body temperature in the hypothalamus2019

    • Author(s)
      小森忠祐、森川吉博
    • Organizer
      A Keystone Symposium [Functional Neurocircuitry of Feeding and Feeding Disorders]
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Functional roles of FGF23-αKlotho axis in the regulation of food intake during fasting2018

    • Author(s)
      小森忠祐、森川吉博
    • Organizer
      A Keystone Symposium [Organ Crosstalk in Obesity and NAFLD]
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 絶食時の視床下部摂食調節機構におけるFGF23/αKlotho系の機能2018

    • Author(s)
      小森忠祐、森川吉博
    • Organizer
      第123回日本解剖学会総会・全国学術集会
    • Related Report
      2018 Annual Research Report
  • [Presentation] 絶食時の視床下部におけるFGF23の摂食調節作用2018

    • Author(s)
      小森忠祐、森川吉博
    • Organizer
      第40回日本生物学的精神医学会・第61回日本神経化学会大会合同年会
    • Related Report
      2018 Annual Research Report
  • [Presentation] Functional roles of FGF23-αKlotho axis in the regulation of food intake during fasting.2018

    • Author(s)
      Komori T, Morikawa Y.
    • Organizer
      A Keystone Symposium [Organ Crosstalk in Obesity and NAFLD]
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research
  • [Presentation] 絶食時の視床下部摂食調節機構におけるFGF23/αKlotho系の機能2018

    • Author(s)
      小森忠祐、森川吉博
    • Organizer
      第123回日本解剖学会総会
    • Related Report
      2017 Research-status Report

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Published: 2017-07-21   Modified: 2021-01-27  

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