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Regulation by Oxidative Stress of CO-and NO-Mediated Signal Transduction in Vascular Cells

Research Project

Project/Area Number 09044253
Research Category

Grant-in-Aid for international Scientific Research

Allocation TypeSingle-year Grants
SectionJoint Research
Research Field Pathological medical chemistry
Research InstitutionUniversity of Tsukuba

Principal Investigator

BANNAI Shiro  Institute of Basic Medical Sciences, University of Tsukuba, Professor, 基礎医学系, 教授 (70019579)

Co-Investigator(Kenkyū-buntansha) マン ジョバンニ・E  キングスカレッジ, ロンドン, 教授
SATO Hideyo  Institute of Basic Medical Sciences, University of Tsukuba, Lecturer, 基礎医学系, 講師 (60235380)
ISHII Tetsuo  Institute of Basic Medical Sciences, University of Tsukuba, Associate Professor, 基礎医学系, 助教授 (20111370)
MANN Giovanni E.  King's College London, Professor
Project Period (FY) 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1997: ¥2,700,000 (Direct Cost: ¥2,700,000)
Keywordsoxidative stress / carbon monoxide / nitrogen monoxide / vascular cells / macrophages / low-density lipoprotein
Research Abstract

Carbon monoxide (CO) and nitric monoxide (NO) play an important role in the physiological regulation of vascular tone and pathogenesis of atherosclerosis. In the present study we have obtained the following results.
1. In human vascular smooth muscle cells, the activity of heme oxygenase, which generates CO,was induced by oxidized LDL and oxidative stress in a time-and dose-dependent manner.
2. In human endothelial cells, the transport activity of arginine was stimulated and the production of NO increased by culturing the cells in higher concentration of glucose.
3. In mouse macrophages, heme oxygenase was induced by oxidized LDL.However, the transport activity of arginine remained unchanged and production of NO was undetectable by oxidized LDL.
From these results, it is suggested that under oxidative stress conditions heme oxygenase induced by oxidative stress increases the production of CO whereas NO is not generated. It is likely that the regulation of CO production is different from that of NO production. CO may function as the modulator of vascular tone under the oxidative stress conditions which are different from those where NO functions. Manuscripts containing these results are in preparation for papers.
In 1998 UK98 Festival supported by the governments of UK and Japan will be held in Japan. In the course of the present joint research, we agreed as one of the events of UK98 Festival to hold a symposium entitled "Regulation of antioxidant system in oxidative stress" at University of Tsukuba, November l998. The British Council has offered a financial support for this symposium.

Report

(2 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • Research Products

    (14 results)

All Other

All Publications (14 results)

  • [Publications] Sato,H.: "Expression of stress proteins heme oxygenase-1 and -2 in acute pancreatitis and pancreatic islet bTC3 and acinar AR42J cells" FEBS Letters. 405. 219-223 (1977)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Ishii,T.: "Low micromolar Levels of hydrogen perxide and preteasome inhitors induce the 60-kDa A170 stress protein in murine peritoneal macrophages." Biochem・Biophys.Res.Commun.232. 33-37 (1977)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Sato,H.: "Induction of the cystine-glutathione antioxidant pathway in pancreatic acinar and islet cells." Digestion. 58(S2). 104-104 (1977)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Tachi,Y.: "High concentration of glucose causes impairment of the funetion of the glutathione redox cycle in human vascular smooth muscle cells." FEBS Letters. 421. 19-22 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Sato,H.: "Mammalian peroxiredoxin MSP23 as an oxidative stress-inducible protein." Redox regulation of cell signaling and its clinical application.ed.by Yodoi,J.and packer,L.(in press). (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Sato, H.et al.: "Expression of stress proteins heme oxygenase-1 and -2 in acute pancreatitis and pancreatic islet beta TC3 and acinar AR42J cells." FEBS Lett.405. 219-223 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Ishii, T.et al.: "Low micromolar levels of hydrogen peroxide and proteasome inhibitors induce the 60-kDa A170 stress protein in murine peritoneal macrophages." Biochem.Biophys.Res.Commun. 232. 33-37 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Sato, H.et al.: "Induction of the cystine-glutathione antioxidant pathway in pancreatic acinar and islet cells." Digestion. 58(S2). 104-104 (1977)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Tachi, Y.et al: "High concentration of glucose causes impairment of the function of glutathione redox cycle in human vascular smooth muscle cells." FEBS Lett.421. 19-22 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Sato, H.et al.: "Mammalian peroxiredoxin MSP23 as an oxidative stress-inducible protein." "Redox regulation of cell signaling and its clinical application" ed.by Yodoi, J.and Packer, L., in press, Marcel Dekker. (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] H. Sato: "Expression of stress proteins heme oxygenase-1 and -2 in acute pancreatitis pancreatic bTC3 and acinar AR42J cel" FEBS Letters. 405. 219-223 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] T. Ishii: "Low micromolar levels of hydrogen peroxide and proteasom inhibitors induce the 60-kDa A170 stress prtein in muriperitoneal macrophage" Biochemical Biophysical Res. Commun.232. 33-37 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] H. Sato: "Induction of the cystine-glutathione antioxidant pathway in pancreatic acinar and islet cells." Digestion. 58 (S2). 104-104 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Y. Tachi: "High concentration of glucose causes impairment of the function of the glutathione redox cycle in human vascula smooth muscle cel" FEBS Letters. 421. 19-22 (1998)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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