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Elucidation of the role of neuropeptides involved in fear memory

Research Project

Project/Area Number 15K01842
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Basic / Social brain science
Research InstitutionChiba University

Principal Investigator

Iwase Katsuro  千葉大学, 大学院医学研究院, 講師 (80322030)

Research Collaborator ASHINO hiromi  
ARITA emiko  
Project Period (FY) 2015-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords記憶・学習 / 恐怖条件付け / 神経ペプチド / 光環境 / 血管新生 / 記憶学習 / 恐怖記憶 / 遺伝的背景 / GPCR / CREB
Outline of Final Research Achievements

Using the secretogranin II gene (Scg2) deficient mice (Scg2 KO), we performed fear conditioning combining footshock (unconditional stimulus) and tone (conditional stimulus), and examined the freezing response. It was found that the Scg2 KO mice tended to suppress the freezing response during the hippocampus-dependent context test. On the other hand, there was no difference between genotypes in sensitivity to electrical stimulation, it was considered that suppression of freezing response was not due to a decrease in sensitivity to stimulation. Moreover, in the chicken embryo chorioallantoic membrane assay, the Scg2-derived neuropeptide secretoneurin exhibited an angiogenesis promoting activity, and the physiological analogy with vascular endothelial growth factor (VEGF) was further confirmed.

Academic Significance and Societal Importance of the Research Achievements

不安・恐怖は、危険を察知し安全を確保する上で重要なものであり、その制御機構の解明は、社会的要請も強い重要な研究課題である。Scg2遺伝子の欠損が恐怖記憶によるすくみ反応の抑制を引き起こすことから、Scg2由来ペプチドの作用の抑制は、不安障害の症状改善につながることが期待される。またScg2由来ペプチド・セクレトニューリンとVEGFの間でみられる多様な生理活性の類似性は、セクレトニューリンの作用を理解する上で重要な特徴である。

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

    (5 results)

All 2019 2018 2017 2016 2015

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (4 results)

  • [Journal Article] Systemic oscillator-driven and nutrient-responsive hormonal regulation of daily expression rhythms for gluconeogenic enzyme genes in the mouse liver.2019

    • Author(s)
      Taira A, Arita E, Matsumoto E, Oohira A, Iwase K, Hiwasa T, Yokote K, Shibata S, Takiguchi M.
    • Journal Title

      Chronobiology International

      Volume: 36(5). Issue: 5 Pages: 591-615

    • DOI

      10.1080/07420528.2019.1570246

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed
  • [Presentation] 血管新生においてCK2によりもたらされるMMP13の調節2018

    • Author(s)
      芦野 洋美、岩瀬 克郎、瀧口 正樹
    • Organizer
      第91回日本生化学会大会
    • Related Report
      2018 Annual Research Report
  • [Presentation] カゼインキナーゼ2の阻害がもたらす血管新生抑制の解析2017

    • Author(s)
      芦野 洋美、岩瀬 克郎、小野 富男、瀧口 正樹
    • Organizer
      2017年度生命科学系学会合同年次大会
    • Related Report
      2017 Research-status Report
  • [Presentation] CK2阻害物質による血管新生促進ケモカインCXCL1作用の抑制2016

    • Author(s)
      芦野洋美,岩瀬克郎,小野富男,瀧口正樹
    • Organizer
      第89回日本生化学会大会
    • Place of Presentation
      仙台国際センター(宮城県仙台市青葉区)
    • Related Report
      2016 Research-status Report
  • [Presentation] 血管新生およびNF-κB活性化を抑制するCK2阻害剤の血管内皮細胞透過性への作用2015

    • Author(s)
      芦野洋美,岩瀬克郎,瀧口正樹
    • Organizer
      第38回日本分子生物学会・第88回日本生化学会合同大会
    • Place of Presentation
      神戸国際展示場(兵庫県神戸市中央区)
    • Year and Date
      2015-12-01
    • Related Report
      2015 Research-status Report

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

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