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Developing new therapy of multiple screlosis using adrenomedullin

Research Project

Project/Area Number 24890267
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Neurology
Research InstitutionKyoto University

Principal Investigator

KITAMURA Akihiro  京都大学, 医学(系)研究科(研究院), 助教 (80636019)

Project Period (FY) 2012-08-31 – 2013-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywords多発性硬化症 / アドレノメデュリン / EAE / VCAM-1 / ICAM-1
Research Abstract

We investigated recombinant human adrenomedullin (AM) for treatment of myelin oligodendrocyte glycoprotein (MOG)-induced experimental autoimmune encephalomyelitis (EAE) in C57BL/6J mice, which is the representative model of multiple sclerosis. Intraperitoneal continuous administration of AM and normal saline for 14 days using osmotic pumps were started concomitant with sensitization of EAE. Temporal changes of the clinical score were evaluated.
In the group of normal saline, clinical scores started to increase on 11 days after sensitization and rapidly got worse. AM significantly reduced clinical scores on between 13 and 16 days but got worse immediately to the level of the other group after the end of administration.
AM was revealed to improve the clinical score of EAE. We will temporally perform histological and immunological evaluation and will explore the possibility of AM to serve as a strategy to tackle multiple sclerosis.

Report

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

    (1 results)

All 2014

All Presentation (1 results)

  • [Presentation] 実験的自己免疫性脳脊髄炎に対する血管作動性ホルモン・アドレノメデュリンの治療効果2014

    • Author(s)
      北村彰浩, 富岳亮, 高橋良輔, 松井真
    • Organizer
      第26回日本神経免疫学会学術集会
    • Place of Presentation
      金沢
    • Related Report
      2013 Final Research Report

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Published: 2012-11-27   Modified: 2019-07-29  

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