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Exploration of analgesic target for tumor-induced neuropathic pain based on the molecular mechanism of circadian rhythm in allodynia

Research Project

Project/Area Number 24390149
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section一般
Research Field Pain science
Research InstitutionKyushu University

Principal Investigator

KOYANAGI Satoru  九州大学, 薬学研究科(研究院), 准教授 (60330932)

Co-Investigator(Renkei-kenkyūsha) TSUDA Makoto  九州大学, 大学院薬学研究院, 教授 (40373394)
MATSUNAGA Naoya  九州大学, 大学院薬学研究院, 助教 (10432915)
Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥14,820,000 (Direct Cost: ¥11,400,000、Indirect Cost: ¥3,420,000)
Fiscal Year 2014: ¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2013: ¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2012: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
Keywords神経障害痛 / 概日時計 / 医薬品開発 / がん性疼痛 / 概日リズム / 時計遺伝子 / 生体リズム / 神経障害疼痛 / アストロサイト / 神経障害性疼痛
Outline of Final Research Achievements

Pain in cancer is often associated with tumor compression or infiltration on tissues. Cancer-related neuropathic pain also arises from injury attributable to infiltration of malignant cells into peripheral nerves. One troublesome hallmark symptom of neuropathic pain is hypersensitivity to normally innocuous stimuli, a condition known as “tactile allodynia” that is refractory even to opioids. The intensity of neuropathic pain in patients with cancer has been known to vary over 24 hour. We aimed to clarify the molecular link connecting the circadian clock to neuropathic pain, and identified a molecule responsible for causing the circadian variation of “allodynia”. Importantly, suppressing the function of the circadian-allodynic molecule resulted in the significant attenuation of neuropathic pain. Identification of mechanism underlying the circadian change in the pathological condition will be useful strategy to discover new therapeutic target.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Annual Research Report
  • 2012 Annual Research Report
  • Research Products

    (9 results)

All 2015 2014 2013

All Journal Article (4 results) (of which Peer Reviewed: 4 results,  Open Access: 2 results,  Acknowledgement Compliant: 1 results) Presentation (5 results) (of which Invited: 2 results)

  • [Journal Article] Modulation of peroxisome proliferator-activated receptor-α activity by bile acids causes circadian changes in the intestinal expression of Octn1/Slc22a4 in mice.2015

    • Author(s)
      Wada E, Koyanagi S, Kusunose N, Akamine T, Masui H, Hashimoto H, Matsunaga N, Ohdo S.
    • Journal Title

      Mol Pharmacol

      Volume: 87 Issue: 2 Pages: 314-322

    • DOI

      10.1124/mol.114.094979

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Renal circadian clock regulates the dosing-time dependency of cisplatin-induced nephrotoxicity in mice.2014

    • Author(s)
      Oda M, Koyanagi S, Tsurudome Y, Kanemitsu T, Matsunaga N, Ohdo S.
    • Journal Title

      Mol Pharmacol

      Volume: 85 Issue: 5 Pages: 715-722

    • DOI

      10.1124/mol.113.089805

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] The intrinsic microglial molecular clock controls synaptic strength via the circadian expression of cathepsin S2013

    • Author(s)
      Hayashi Y, Koyanagi S, Kusunose N, Okada R, Wu Z, Tozaki-S aitoh H, Ukai K, Kohsaka S, Inoue K. Ohdo S. Nakanishi H.
    • Journal Title

      Scientific Reports

      Volume: vol.3 Issue: 1 Pages: 1-7

    • DOI

      10.1038/srep02744

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Rhythmic control of the ARF-MDM2 pathway by ATF4 underlies cireadian accumulation2013

    • Author(s)
      Horiguchi M, Koyanagi S, et al
    • Journal Title

      Cancer Research

      Volume: 73

    • Related Report
      2012 Annual Research Report
    • Peer Reviewed
  • [Presentation] Glucocorticoid regulation of circadian rhythm in neuropathic pain2014

    • Author(s)
      楠瀬直喜、久保田敏昭
    • Organizer
      第21回日本時間生物学会学術大会
    • Place of Presentation
      福岡市(九州大学)
    • Year and Date
      2014-11-07 – 2014-11-09
    • Related Report
      2014 Annual Research Report
    • Invited
  • [Presentation] Exploration of analgesic target for neurophatic pain based on the molecular mechanism of circadian rhythm in allodynia2014

    • Author(s)
      小柳悟、楠瀬直喜、大戸茂弘
    • Organizer
      The 87th Annual Meeting of the Japanese Biochemical Society
    • Place of Presentation
      京都市(京都国際会議場)
    • Year and Date
      2014-10-15 – 2014-10-18
    • Related Report
      2014 Annual Research Report
    • Invited
  • [Presentation] 神経障害性疼痛の概日リズム形成メカニズムと鎮痛標的分子の探索2014

    • Author(s)
      小柳悟、楠瀬直喜、松永直哉、大戸茂弘
    • Organizer
      日本薬学会第134年会
    • Place of Presentation
      熊本市(熊本大学)
    • Related Report
      2013 Annual Research Report
  • [Presentation] Molecular basis for circadian regulation of neuropathic pain in mice2013

    • Author(s)
      Kusunose N, Koyanagi S, et al
    • Organizer
      第86回日本薬理学会年会
    • Place of Presentation
      福岡市
    • Year and Date
      2013-03-21
    • Related Report
      2012 Annual Research Report
  • [Presentation] 神経障害性疼痛の概日リズム制御に関わるグルココルチコイド標的遺伝子の探索2013

    • Author(s)
      楠瀬直喜、小柳悟、松永直哉、大戸茂弘
    • Organizer
      第20回日本時間生物学会学術大会
    • Place of Presentation
      大阪市(近畿大学)
    • Related Report
      2013 Annual Research Report

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Published: 2012-04-24   Modified: 2019-07-29  

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