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Cathepsin K inhibitor regulates inflammation and bone destruction in experimentally-induced rat periapical lesions.

Research Project

Project/Area Number 15K11106
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Conservative dentistry
Research InstitutionShowa University (2016-2018)
Tokyo Medical and Dental University (2015)

Principal Investigator

SUZUKI NORIYUKI  昭和大学, 歯学部, 准教授 (20372451)

Co-Investigator(Kenkyū-buntansha) 川島 伸之  東京医科歯科大学, 大学院医歯学総合研究科, 講師 (60272605)
Research Collaborator IKEDA Megumi  
Project Period (FY) 2015-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords根尖性歯周炎 / カテプシンK / カテプシンK阻害 / 抗RANKL抗体 / カテプシンK
Outline of Final Research Achievements

We evaluated the effects of cathepsin K inhibitor on inflammation and bone destruction in experimentally-induced rat periapical lesions. The size of the periapical lesion, number of tartrate-resistant acid phosphatase-positive osteoclasts and major histocompatibility complex class II molecule-expressing macrophages in the experimental group decreased significantly when compared with the control group. The expression of pro-inflammatory cytokines in the experimental group was significantly suppressed when compared with the control group. These results suggest that the cathepsin K inhibitor may inhibit not only cathepsin K activity in osteoclasts but also inflammatory mediator synthesis relating to osteoclastogenesis, and these synergistic effects may be involved in the suppression of periapical lesion expansion.

Academic Significance and Societal Importance of the Research Achievements

根尖性歯周炎は、根尖歯周組織に生じる炎症性骨吸収性疾患であるが、その病態の判定は困難であり、慢性化すると難治性となることも少なくない。本研究はカテプシンK阻害剤の抗炎症作用に着目し、根尖性歯周炎の抑制に応用しようとするものである。本研究により、薬剤によって根尖性歯周炎を抑制できる可能性が示唆されたことにより、将来的に難治性根尖性歯周炎を速やかに治癒に導く可能性が開ければ、国民の口腔の健康増進に与える影響は大きいものと思われる。

Report

(5 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (4 results)

All 2015

All Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (3 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] Cathepsin K inhibitor regulates inflammation and bone destruction in experimentally induced rat periapical lesions2015

    • Author(s)
      Suzuki N, Takimoto K, Kawashima N
    • Journal Title

      Journal of Endodontics

      Volume: 41 Issue: 9 Pages: 1474-1479

    • DOI

      10.1016/j.joen.2015.04.013

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] Effects of short-period three-dimensional spheroid culture for odonto-/osteoblastic differentiation of dental pulp cells2015

    • Author(s)
      Yamamoto M, Hashimoto K, Bakhit A, Suzuki N, Kawashima N, Okiji T
    • Organizer
      European Society of Endodontology
    • Place of Presentation
      Barcelona
    • Year and Date
      2015-09-19
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] Osr2はマウス歯乳頭細胞の硬組織形成細胞への分化を促進する2015

    • Author(s)
      川島伸之、橋本健太郎、山本弥生子、辺見浩一、鈴木規元、興地隆史
    • Organizer
      第36回日本歯内療法学会学術大会
    • Place of Presentation
      神奈川
    • Year and Date
      2015-07-11
    • Related Report
      2015 Research-status Report
  • [Presentation] 歯髄組織および歯肉組織より得られた間葉系幹細胞の硬組織形成細胞への分化能の比較2015

    • Author(s)
      川島伸之、山本弥生子、橋本健太郎、Bakhit A、小泉悠、辺見浩一、大井智恵、鈴木規元、興地隆史
    • Organizer
      第142回日本歯科保存学会春季大会
    • Place of Presentation
      福岡
    • Year and Date
      2015-06-25
    • Related Report
      2015 Research-status Report

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Published: 2015-04-16   Modified: 2020-03-30  

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