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2012 Fiscal Year Final Research Report

Understanding of molecular mechanism and development of prediction system of drug- induced hepatotoxicity, focusing on the inflammation-associated nuclear receptors and cell-cell interactions.

Research Project

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Project/Area Number 23659072
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Medical pharmacy
Research InstitutionTohoku University

Principal Investigator

YOSHINARI Kouichi  東北大学, 大学院・薬学研究科, 准教授 (60343399)

Project Period (FY) 2011 – 2012
Keywords医薬品情報 / 安全性学
Research Abstract

In this study, we have investigated the influences of treatment with the activators of inflammation-associated nuclear receptors on the gene expression profile of inflammation-related genes in human model macrophages and rat Kupffer cells. The results suggest that the activation of either PXR, CAR, LXRα, PPAR or PPARγ elicits the changes in the gene expression of the several genes investigated, that the influence is dependent on the nuclear receptors, and that the changes are regulated at the transcriptional levels. These imply that not only parenchymal hepatocytes but non-parenchymal hepatocytes are targets for the drug- or xenobiotic-induced liver inflammation.

  • Research Products

    (2 results)

All 2011

All Presentation (2 results)

  • [Presentation] ヒトマクロファージ様細胞における炎症関連遺伝子発現に対する核内受容体リガンドの影響2011

    • Author(s)
      平田貴大、吉成浩一、山添康
    • Organizer
      日本薬学会東北支部大会
    • Place of Presentation
      仙台市
    • Year and Date
      2011-10-30
  • [Presentation] 化学物質の有害性を左右する核内受容体:毒性発現メカニズムの理解と有害性評価への応用を目指して2011

    • Author(s)
      吉成浩一
    • Organizer
      第10回日本化学工業協会LRI研究報告会
    • Place of Presentation
      東京(招待講演)
    • Year and Date
      2011-08-26

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Published: 2014-09-25  

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