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1999 Fiscal Year Final Research Report Summary

Induction of apoptosis and cell injury in kidney by active oxygen species produced by cytochrome P450

Research Project

Project/Area Number 10670094
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General pharmacology
Research InstitutionOsaka City University

Principal Investigator

IMOKA Susumu  Medical School, Associate Professor, 医学部, 助教授 (60145795)

Project Period (FY) 1998 – 1999
Keywordscytochrome P450 / super oxide / hypoxia / kidney / blood vessel
Research Abstract

Diabetes and arteriosclerosis induce cell injury in a kidney and a blood vessel. Free radicals are thought to play an important role in such pathway but its mechanism isn't well understood. Cytochrome P450(P450) which is a monooxygenase produces active oxygen species. Active oxygen species cause DNA oxidation and lipid peroxidation and also induce apoptosis. In this study, a role of active oxygen species produced by P450s in apoptosis and gene expression was investigated. Phenobarbital (PB), an inducer of P450s, induced production of active oxygen, and 8-OHdG (a DNA oxidation marker). PB also induced proto-oncogene, c-myc and apoptosis, DNA fragmentation. Ketoconazole, an inhibitor of P450, inhibited all these pathways. Furthermore, Hep 3B, hepatoma cell line, and primary culture of rat aorta were used to investigate ischemic injury of cell. Reduction of oxygen tension (20% to 1%) induced production of superoxide and also induced heme oxygenase (in both cells) and erythropoietin genes (in Hep 3B). DPIC, an inhibitor of NAD(P)H-dependent enzymes, decreased expression of these genes.
These findings suggest that active oxygen species produced by P450s induced apotosis and several gene expression. P450 has an important role in this pathway.

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] M. Nakamura, S. Imaoka et al.: "P450 isoforms in a murine macrophage cell line, RAW264.7, and changes in the levels of P450 isoforms by activation with LPS and INF-γ"Biochem. Biophys. Acta. 1385. 101-106 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] M. Kitano et al.: "Presence of a threshold for promoting effects of phenobarbital on diethylnitrosamine-induced hepatic foci in the rat"Carcinogenesis. 19. 1475-1480 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S. Takemura, Y. Minamiyama, S. Imaoka et al.: "Hepatic cytochrome P450 is directly inactivated by nitric oxide, not by inflammatory cytokines, in the early phase of endotoxemia"J. Hepatol.. 30. 1035-1044 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Y. Minamiyama et al.: "Isoforms of cytochrome P450 on organic nitrate-derived nitric oxide release in human heart"FEBS Lett.. 452. 165-169 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T. Ichihara et al.: "Inhibition of liver glutathione S-transferase placental form-positive foci deelopment in the rat hepatocarcinogenesis by Porphyra tenera (Asakusa-nori)"Cancer Lett.. 141. 211-218 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K. Ayajiki et al.: "Inolvement of CYP3A-derived arachidonic acidmetabolite(s) in responeses to endothelium-derived K^+ -channel opening substance in monkey lingual artery"Br. J. pharmacol.. 128. 802-808 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] M.Nakamura, S.Imaoka, F.Amano, and Y.Funae: "P450 isoforms in a murine macrophage cell line, RAW264.7, and changes in the levels of P450 isoforms by activation with LPS and INF-γ"Biochem.Biophys.Acta. 1385. 101-106 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] M.Kitano, T.Ichihara, T.Matsuda, H.Wanibuchi, S.Tamano, A.Hagiwara, S.Imaoka, Y.Funae, T.Shirai, and S.Fukushima: "Presence of a threshold for promoting effects of phenobarbital on diethylnitrosamine-induced hepatic foci in the rat"Carcinogenesis. 19. 1475-1480 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S.Takemura, Y.Minamiyama, S.Imaoka, Y.Funae, K.Hirohashi, M.Inoue, and H.Kinoshita: "Hepatic cytochrome P450 is directly inactivated by nitric oxide, not by inflammatory cytokines, in the early phase of endotoxemia"J.Hepatol. 30. 1035-1044 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Y.Minamiyama, S.Takemura, T.Akiyama, S.Imaoka, M.Inoue, Y.Funae, and S.Okada: "Isoforms of cytochrome P450 on organic nitrate-derived nitric oxide release in human heart"FEBS Lett. 452. 165-169 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T.Ichihara, H.Wanibuchi, T.Taniyama, Y.Okai, Y.Yano, S.Otani, S.Imaoka, Y.Funae, and S.Fukushima: "Inhibition of liver glutathione S-transferase placental form-positive foci development in the rat hepatocarcinogenesis by Porphyra tenera (Asakusa-nori)"Cancer Lett.. 141. 211-218 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Ayaiji, T.Okamura, H.Fujioka, S.Imaoka, Y.Funae, and N.Toda: "Involvement of CYP3A-derived arachidonic acid metabolite(s) in responses to endothelium-derived KィイD1+ィエD1-channel opening substance in monkey lingual artery"Br.J.Pharmacol.. 128. 802-808 (1999)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2001-10-23  

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