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Attenuation of intervertebral disc degeneration and osteophyte formation via inhibition of Hedgehog signaling

Research Project

Project/Area Number 17K10952
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Orthopaedic surgery
Research InstitutionUniversity of Occupational and Environmental Health, Japan

Principal Investigator

NAKAMURA EIICHIRO  産業医科大学, 医学部, 准教授 (10412644)

Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2017: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords椎間板変性 / Hedgehog / Smoothened / 骨棘 / Sonidegib / 骨・軟骨代謝学 / Cre / 脊椎脊髄病 / 骨・軟膏代謝学
Outline of Final Research Achievements

We investigated whether inhibition of smoothened (Smo), a key component of hedgehog pathway in the process of endochondral ossification and intervertebral disc development, attenuates intervertebral disc degeneration in the degenerative spine model. Mice were intraperitoneally administered saline or Sonidegib, an antagonist of Smo, 3 times per week after operation for 10 weeks. Disc height reduction rate and Masuda classification score was significantly suppressed in Sonidegib group against the saline group at 10 weeks after operation. Saline group showed severe intervertebral disc degeneration, collapse of vertebral end plate layer, hypertrophic changes of chondrocytes in the vertebral end plate cartilage and osteophyte formation in the corner of vertebra. In contrast, all these phenomena were attenuated in the mice with administration of Sonidegib, indicating that hedgehog signaling has a crucial role in the degenerative spondylosis of spine.

Academic Significance and Societal Importance of the Research Achievements

加齢に伴い椎間板変性が起こり腰痛や脊柱管狭窄、椎間不安定性、脊柱変形を引き起こし多くの脊椎疾患の原因となる。椎間板の発生や変性過程で発現するヘッジホグシグナルを伝達する膜蛋白のスムースンドの阻害薬であるソニデジブを椎間板変性モデルのマウスに腹腔内投与したところ、椎間板変性の抑制効果が見られた。ソニデジブは癌治療薬としてすでに臨床試験中の薬剤であり、超高齢社会で脊椎加齢変性疾患に対する抑制治療への応用が期待される。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (5 results)

All 2019 2018 2017

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (4 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] Attenuation of Post‐Traumatic Osteoarthritis After Anterior Cruciate Ligament Injury Via Inhibition of Hedgehog Signaling2019

    • Author(s)
      Takada Shinichiro、Nakamura Eiichiro、Sabanai Ken、Tsukamoto Manabu、Otomo Hajime、Kanoh Shinkichi、Murai Teppei、Fukuda Hokuto、Okada Yasuaki、Uchida Soshi、Sakai Akinori
    • Journal Title

      Journal of Orthopaedic Research

      Volume: 38 Issue: 3 Pages: 609-619

    • DOI

      10.1002/jor.24494

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Presentation] Attenuation of Intervertebral disc degeneration and osteophyte formation via inhibition of hedgehog signaling2019

    • Author(s)
      Hokuto Fukuda, Eiichiro Nakamura, Ken Sabanai, Manabu Tsukamoto, Yasuaki Okada, Shinichiro Takada, Akinori Sakai
    • Organizer
      EUROSPINE 2019
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Hedgehog pathwayの阻害は椎間板変性と椎体骨棘形成を抑制する2019

    • Author(s)
      福田北斗・中村英一郎・佐羽内研・塚本 学・岡田祥明・酒井昭典
    • Organizer
      第4回黒潮カンファランス
    • Related Report
      2019 Annual Research Report
  • [Presentation] 変形性脊椎症における椎間板変性と椎体骨棘形成にはHedgehogシグナルが関与する2018

    • Author(s)
      福田北斗、中村英一郎、 佐羽内 研, 塚本 学, 田島 貴文, 大隈 加代子, 岡田 祥明, 山根 宏敏, 酒井 昭典
    • Organizer
      第47回日本脊椎脊髄病学会学術集会
    • Related Report
      2018 Research-status Report
  • [Presentation] 椎間板変性と椎体骨棘形成にはHedgehogシグナルが関与する2017

    • Author(s)
      福田北斗、中村英一郎、佐羽内研、塚本学、田島貴文、大隈加代子、岡田祥明、酒井昭典
    • Organizer
      第32回日本整形外科学会 基礎学術集会
    • Related Report
      2017 Research-status Report

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Published: 2017-04-28   Modified: 2021-02-19  

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