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The enzyme of Keratan sulfate degradation contributes the functional recovery after thoracic spinal cord injury

Research Project

Project/Area Number 26462237
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Orthopaedic surgery
Research InstitutionNagoya University

Principal Investigator

Imagama Shiro  名古屋大学, 医学部附属病院, 講師 (40467288)

Co-Investigator(Kenkyū-buntansha) 伊藤 全哉  名古屋大学, 医学部附属病院, 医員 (50447819)
安藤 圭  名古屋大学, 医学部附属病院, 助教 (40566973)
伊藤 研悠  名古屋大学, 医学部附属病院, 医員 (10732638)
石川 喜資  名古屋大学, 医学部附属病院, 医員 (30732656)
小林 和克  名古屋大学, 医学部附属病院, 病院助教 (00706294)
都島 幹人  名古屋大学, 医学部附属病院, 医員 (60755338)
Project Period (FY) 2014-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywordsケラタン硫酸 / ケラタン硫酸分解酵素 / 脊髄損傷 / 軸索伸長 / 神経保護 / 感覚障害 / リハビリテーション / 脊髄損傷治療 / トレーサー試験 / ケラタナーゼ / 運動機能回復効果
Outline of Final Research Achievements

We have investigated the efficacy of the enzyme of Keratan Sulfate degradation (KSase) with rehabilitation for rat thoracic spinal cord injury model. The histological analysis including tracer analysis, neurophysiological examination, and sensory examination were performed. From the result of the number of fibers strained for GAP-43, 5-HT, and tracer with DiI, KSase significantly promoted axonal regrowth after SCI. The sensory function was also recovered by KSase treatment without allodynia. There was no adverse effect after KSase treatment. To the subacute phase, the impact of rehabilitation for spinal cord injury was also observed, but limited in chronic phase after spinal cord injury.
KSase may promote not only axonal regrowth but also neural plasticity related to motor and sensory function. The KSase may contribute a satisfactory treatment for spinal cord injury.

Report

(5 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (9 results)

All 2018 2017 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (8 results) (of which Int'l Joint Research: 2 results)

  • [Journal Article] Lack of Fgf18 causes abnormal clustering of motor nerve terminals at the neuromuscular junction with reduced acetylcholine receptor clusters.2018

    • Author(s)
      Ito K, Ohkawara B, Yagi H, Nakashima H, Tsushima M, Ota K, Konishi H, Masuda A, Imagama S, Kiyama H, Ishiguro N, Ohno K.
    • Journal Title

      Sci Rep.

      Volume: 11 Pages: 1-12

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] Drug X can inhibit apoptotic cell death induced by oxidative stress in vitro and improve locomotor function of lower limbs in spinal cord injury model mice in vivo.2017

    • Author(s)
      Mikito Tsushima, Shiro Imagama, Bisei Ohkawara, Naoki Ishiguro, Kinji Ohno
    • Organizer
      Eurospine 2017
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Pathophysiological analysis of skeletal muscles in spinal bulbar muscular atrophy genome editing of CAG repeats2017

    • Author(s)
      Satoshi Tanaka, Takuji Ito, Akinobu Ota, Takefumi Sone, Daisuke Shimojo, Shiro Imagama, Yoshitaka Hosokawa, Manabu Doyu, Hideyuki Okano, Yohei Okada
    • Organizer
      Society for Neuroscience 2017
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] :bFGF様新規化合物の経静脈投与による脊髄損傷治療-これまでの知見と今後の展望2015

    • Author(s)
      今釜史郎
    • Organizer
      第30回日本整形外科学会基礎学術集会
    • Place of Presentation
      富山県富山市富山国際会議場
    • Year and Date
      2015-10-22
    • Related Report
      2015 Research-status Report
  • [Presentation] Role of Fgf18 in motor neurons of the spinal cord2015

    • Author(s)
      伊藤研悠、今釜 史郎, 伊藤 全哉, 安藤 圭、小林 和克, 八木 秀樹, 飛田 哲朗, 伊藤 研悠, 石川 喜資, 都島 幹人, 松本 明之,石黒 直樹
    • Organizer
      Annual Meeting of ORS
    • Place of Presentation
      MGM Grand Hotel(ラスベガス,アメリカ)
    • Year and Date
      2015-03-24 – 2015-03-31
    • Related Report
      2014 Research-status Report
  • [Presentation] The effects of the combination treatment of keratan sulfate digestion and rehabilitation in rat spinal cord injury2014

    • Author(s)
      Y.ISHIKAWA, S. IMAGAMA Z. ITO, K. ANDO, N. ISHIGURO, K. KADOMATSU
    • Organizer
      Neuroscience 2014
    • Place of Presentation
      Walter E. Washington Convention Center (ワシントンDC,アメリカ)
    • Year and Date
      2014-11-15 – 2014-11-19
    • Related Report
      2014 Research-status Report
  • [Presentation] 脊髄損傷再生メカニズムと医療への応用 bFGF様新規化合物による脊髄損傷治療 これまでの知見と今後の展開2014

    • Author(s)
      今釜 史郎, 伊藤 全哉, 安藤 圭, 小林 和克, 八木 秀樹, 飛田 哲朗, 伊藤 研悠, 石川 喜資, 村山 宣人, 門嶋 大輔, 荻野 涼子, 上野 新也, 井上 照好, 森田 泰博, 石黒 直樹
    • Organizer
      第29回日本整形外科学会基礎学術集会
    • Place of Presentation
      城山観光ホテル(鹿児島県鹿児島市)
    • Year and Date
      2014-10-09 – 2014-10-10
    • Related Report
      2014 Research-status Report
  • [Presentation] 脊髄において特異的発現パターンを有するFgf18の運動神経細胞に対する役割2014

    • Author(s)
      伊藤 研悠, 大河原 美静, 中島 宏彰, 今釜 史郎, 八木 秀樹, 飛田 哲朗, 都島 幹人, 石黒 直樹, 大野 欽司
    • Organizer
      第29回日本整形外科学会基礎学術集会
    • Place of Presentation
      城山観光ホテル(鹿児島県鹿児島市)
    • Year and Date
      2014-10-09 – 2014-10-10
    • Related Report
      2014 Research-status Report
  • [Presentation] 脊髄再生の足場となる新規自己集合体ペプチドの効果 グリア性瘢痕は減少し、軸索伸長を許容する2014

    • Author(s)
      安藤 圭, 今釜 史郎, 伊藤 全哉, 小林 和克, 鵜飼 淳一, 新城 龍一, 八木 秀樹, 飛田 哲朗, 伊藤 研悠, 石川 喜資, 都島 幹人, 松本 明之, 西田 佳弘, 石黒 直樹
    • Organizer
      第29回日本整形外科学会基礎学術集会
    • Place of Presentation
      城山観光ホテル(鹿児島県鹿児島市)
    • Year and Date
      2014-10-09 – 2014-10-10
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2019-03-29  

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