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2011 Fiscal Year Final Research Report

Effect of oxidative stress on disulfide bond formation of uric acid efflux transporter BCRP

Research Project

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Project/Area Number 22890003
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Applied pharmacology
Research InstitutionHokkaido University

Principal Investigator

OGURA Jiro  北海道大学, 大学院・薬学研究院, 助教 (20580640)

Project Period (FY) 2010 – 2011
Keywords痛風 / キサンチンオキシダーゼ / 活性酸素 / トランスポータ / ジスルフィド結合
Research Abstract

In this study, we investigated that oxidative stress affected BCRP expression, which is a uric acid efflux transporter. It has known that aging-induced oxidative stress is caused by activation of xanthine oxidase. Thus, we used the substrates of xanthine oxidase in this study. In Caco-2 cells, the activation of xanthine oxidase was suppressed the BCRP S-S bond formation, but not in HK-2 cells. These results suggest that the effect of oxidative stress on the efflux of uric acid is different between intestine and kidney.

  • Research Products

    (1 results)

All 2012

All Journal Article (1 results)

  • [Journal Article] (1st/14) Intestinal ischemia-reperfusion increases efflux for uric acid via paracellular route in the intestine, but decreases that via transcellular route mediated by Bcrp2012

    • Author(s)
      Ogura J
    • Journal Title

      J. Pharm. Pharm. Sci

      Volume: 15 Pages: 295-304

    • URL

      http://ejournals.library.ualberta.ca/index.php/JPPS/article/view/12242

URL: 

Published: 2013-07-31  

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