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Role of reactive oxygen intermediates in lipopolysaccharidemediated hepatic injury in the rat

Research Project

Project/Area Number 05671034
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field General surgery
Research InstitutionKansai Medical University

Principal Investigator

TAKEYAMA Naoshi  Kansai Medical University, 医学部, 講師 (00155053)

Project Period (FY) 1993 – 1995
Project Status Completed (Fiscal Year 1995)
Budget Amount *help
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1995: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1994: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1993: ¥800,000 (Direct Cost: ¥800,000)
Keywordstungsten / aminotriazole / xanthine dehydrogenase / xanthine oxidase / Hydrogen peroxide / lipopolysaccharide / lipopolysaccharide / BALF / NOS inhibitor / PAF / グルタチオンモノエステル
Research Abstract

Since reactive oxygen intermediates derived from xanthine oxidase may have an important role in the pathophysiology of lipopolysaccharide-mediated tissue injury, we studied hydrogen peroxide generation using 3-amino-1,2,4-triazole inactivation of hepatic catalase and the ratio of xanthine oxidase to xanthine dehydrogenase activity in rat livers after in vivo lipopolysaccharide administration. We also studied the effect of tungsten, a potent inhibitor of xanthine oxidase, on the toxicity of lipopolysaccharide. There was increased hydrogen peroxide production and enhanced proteolytic conversion from xanthine dehydrogenase to xanthine oxidase in rat livers after lipopolysaccharide administration. Feeding rats a tungsten-rich diet for 4 weeks greatly diminished hepatic xanthine oxidase activity and lessened the rise in intracellular hydrogen peroxide production after lipopolysaccharide treatment. Liver damage, as assessed by the serum transaminase levels and mortality, was also ameliorated by the tungsten-rich diet. These findings suggest that hydrogen peroxide derived from xanthine oxidase contributes to the development of systemic toxicity and liver damage after lipopolysaccharide administration.

Report

(4 results)
  • 1995 Annual Research Report   Final Research Report Summary
  • 1994 Annual Research Report
  • 1993 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Noshi Takeyama: "Oxidative damage to mitochondria is mediated by the Ca2+-dependent inner membrane permeability transition." Biochemical Journal. 294. 719-725 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] 正司義和: "ARDSにおける顆粒球エラスターゼ、IL6の関与と凝固系への影響" ICUとCCU. 19. 333-337 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Naoshi Takeyama, Yoshikazu Shoji, Kaoru Ohahi and Takaya Tanaka.: "Role of reactive oxygen intermediates in lipopolysaccharide-mediated hepatic injury in the rat." Journal of Surgical Research.60. 258-262 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary

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Published: 1993-04-01   Modified: 2016-04-21  

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