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Functional Analysis of GPR143 in Pulmonary Hypertension

Research Project

Project/Area Number 15K21271
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Anesthesiology
General pharmacology
Research InstitutionYokohama City University

Principal Investigator

KOGA Motokazu  横浜市立大学, 医学部, 助教 (00637233)

Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2017: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords肺高血圧症 / L-DOPA / GPR143 / モノクロタリン / DOPA / 肺高血圧
Outline of Final Research Achievements

We have been working that L-DOPA, a dopamine precursor has unique physiological activity. In 2017, Masukawa reported that L-DOPA receptor candidate, GPR-143, interact with alpha adrenergic receptor and modulating its action. Therefore, we have investigated at first that L-DOPA has any interaction to vasoconstriction of pulmonary artery. As a result we found that L-DOPA also enhance phenylephrine induced vasoconstriction in pulmonary artery. Moreover, interestingly, this action is attenuated in early stage of monocrotaline-induced pulmonary hypertensive rat model. This findings may yield novel pathological and therapeutic finding in pulmonary hypertension.

Report

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

    (1 results)

All 2017

All Presentation (1 results)

  • [Presentation] L-DOPAの肺高血圧モデル肺血管におけるフェニレフリン応答の修飾作用2017

    • Author(s)
      古賀資和、増川太輝、中村史雄、菅原陽、水野祐介、後藤隆久、五嶋良郎
    • Organizer
      第136回日本薬理学会関東部会
    • Related Report
      2017 Annual Research Report

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Published: 2015-04-16   Modified: 2019-03-29  

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