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The construction of combination therapy of exercise and medication on DCM model mice

Research Project

Project/Area Number 18K17686
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 59010:Rehabilitation science-related
Research InstitutionJuntendo University

Principal Investigator

Sugihara Masami  順天堂大学, 医学部, 助教 (80648163)

Project Period (FY) 2018-04-01 – 2022-03-31
Project Status Completed (Fiscal Year 2021)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2020: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords運動療法 / 拡張型心筋症 / 心不全 / 心室性不整脈 / レニン・アンギオテンシン阻害薬 / 不整脈
Outline of Final Research Achievements

Dilated cardiomyopathy (DCM) is one of major causes of heart failure (HF). Today, exercise is regarded as one of therapies for HF. However, the effects of exercise on patients with DCM have not been established. A knock-in mouse model of human inherited DCM is useful for investigating inherited DCM. Homozygous mice were divided into four groups based on the administration of angiotensin receptor antagonist (ARB) and voluntary exercise: without drug or exercise control, oral administration of ARB, daily exercise and both of ARB and exercise (BOTH). The all groups started medication and running at 1 month of age. At the 2.5 months of age, mice were sacrificed after an investigation with echocardiography. BOTH group was significantly improved in ejection fraction. On the other hand, exercise group showed less E/e’ than the other groups, The wights of soleus muscles in the exercise group were more increased than BOTH group and were thought to be associated with diastolic function.

Academic Significance and Societal Importance of the Research Achievements

研究代表者は、循環器内科医としての診療の中でDCMでも適切な運動の効果が推測された症例を経験している。しかし、多くのDCM患者においては、進行してから受診する例が多く運動療法を試みる機会を逸しやすい、易不整脈性のため運動プロトコルが決めにくい、環境や遺伝的要因、薬物介入によるバラつきが大きい、という点で評価が難しい状況が続いている。
本研究では、遺伝的背景の均一なモデル動物を解析できるので効果を定量的に検討できる。また、近年発達している遺伝子診断と合わせ、病態進行に合わせた運動療法のプロトコルの確立に寄与することが期待できる。

Report

(5 results)
  • 2021 Annual Research Report   Final Research Report ( PDF )
  • 2020 Research-status Report
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (4 results)

All 2021 2020

All Presentation (4 results)

  • [Presentation] 拡張型心筋症モデルマウスにおける自発運動の効果2021

    • Author(s)
      杉原匡美、柿木亮、村山尚、三井田孝、櫻井隆、森本幸生、呉林なごみ
    • Organizer
      第7回日本筋学会学術集会
    • Related Report
      2021 Annual Research Report
  • [Presentation] 拡張型心筋症モデルにおける性差による自発運動の効果の違い2020

    • Author(s)
      杉原匡美, 柿木亮, 村山尚, 平山哲, 三井田孝, 森本幸生, 呉林なごみ
    • Organizer
      第67回日本臨床検査医学会学術集会
    • Related Report
      2020 Research-status Report
  • [Presentation] 拡張型心筋症モデルマウスにおける性差による自発運動の効果の違い2020

    • Author(s)
      杉原匡美, 柿木亮, 村山尚, 三井田孝,櫻井隆, 森本幸生, 呉林なごみ
    • Organizer
      第94回日本薬理学会年会
    • Related Report
      2020 Research-status Report
  • [Presentation] 拡張型心筋症モデルマウスにおける性差による自発運動の効果の違い2020

    • Author(s)
      杉原匡美、柿木亮、村山尚、三井田孝、櫻井隆、森本幸生、呉林なごみ
    • Organizer
      第93回日本薬理学会年会(紙上開催)
    • Related Report
      2019 Research-status Report

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Published: 2018-04-23   Modified: 2023-01-30  

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