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NSAIDs inhibit forming oligomers and fibrils by binding to the structure of <beta>-amyloid and <alpha>-synuclein protein aggregates

Research Project

Project/Area Number 17H06498
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Chemical biology
Research InstitutionHirosaki University

Principal Investigator

Hirohata Mie  弘前大学, 医学研究科, 助教 (50806552)

Research Collaborator Shoji Mikio  
Sato Kaoru  
Project Period (FY) 2017-08-25 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywordsケミカルバイオロジー / 蛋白凝集 / アミロイドβ / αシヌクレイン / オリゴマー / 分子間相互作用 / アルツハイマー病 / パーキンソン病 / 脳神経疾患 / 蛋白質凝集 / 有機化学 / 蛋白質
Outline of Final Research Achievements

The oligomeric forms of amyloid β-protein (Aβ) or α-synuclein (αS) play a critical role in the development of Alzheimer’s disease (AD) or Parkinson’s disease (PD). Epidemiological studies have revealed that therapeutic use of non-steroidal anti-inflammatory drugs (NSAIDs) reduces the risk of developing AD and PD. We show that NSAIDs have anti-oligomerization and anti-fibrillization effects on Aβ(1-40), Aβ(1-42) and αS in vitro at physiological pH and temperature, by using nucleation-dependent polymerization monitored by thioflavin fluorescence, atomic force microscopy, electron microscopy, and photo-induced cross-linking of unmodified proteins (PICUP) followed by SDS-PAGE. Three-dimensional fluorescence spectroscopic analyses demonstrated that some NSAIDs interacted with Aβs or αS oligomers. We speculated that NSAIDs inhibit forming oligomers and fibrils by binding to the structure of their aggregates. NSAIDs could be key molecules for the preventive agents for AD and PD.

Academic Significance and Societal Importance of the Research Achievements

本研究の成果から,NSAIDsはアルツハイマー病およびパーキンソン病の予防薬および病態修飾薬の有力な候補分子となる可能性があることが示唆された.この分野の検討は,これまで国際的にも報告がなく,NSAIDsとの分子間相互作用に基づいたアルツハイマー病およびパーキンソン病の病態修飾薬を開発する上でも極めて重要な貢献ができると考えられる.

Report

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

    (3 results)

All 2019 2018

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

  • [Journal Article] Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease2019

    • Author(s)
      Preische Oliver、Kazushi Suzuki (83/91, alphabetical order) et al. Dominantly Inherited Alzheimer Network
    • Journal Title

      Nature Medicine

      Volume: 25 Issue: 2 Pages: 277-283

    • DOI

      10.1038/s41591-018-0304-3

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] NSAIDs inhibit forming oligomers and fibrils by binding to the structure of α-synuclein aggregates2019

    • Author(s)
      Mie Hirohata
    • Organizer
      第60回日本神経学会学術大会
    • Related Report
      2018 Annual Research Report
  • [Book] 精神科2018

    • Author(s)
      廣畑美枝,東海林幹夫
    • Publisher
      科学評論社
    • Related Report
      2018 Annual Research Report

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Published: 2017-08-25   Modified: 2021-01-27  

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