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Virchows Archiv

, Volume 438, Issue 3, pp 259–270 | Cite as

Pulmonary carcinogenesis induced by ferric nitrilotriacetate in mice and protection from it by Brazilian propolis and artepillin C

  • Tetsuo Kimoto
  • Satomi Koya-Miyata
  • Keiko Hino
  • Mark  J. Micallef
  • Toshiharu Hanaya
  • Shigeyuki Arai
  • Masao Ikeda
  • Masashi Kurimoto
Original Article

Abstract.

In experiments using the renal carcinogen ferric nitrilotriacetate (Fe-NTA) in male ddY mice, primary pulmonary cancers were also induced in bronchiolar and alveolar tissues. 4-Hydroxy-2-nonenal (4-HNE) and 8-hydroxy-2'-deoxyguanosine (8-OHdG), products of oxidative processes, increased in bronchiolar and alveolar cells after administration of Fe-NTA. These substances disappeared after oral administration of propolis or artepillin C, as shown histochemically, and correlated with an anticancer prophylactic effect of propolis and artepillin C. From our investigation, lipid peroxidation seems to play an important role in pulmonary carcinogenesis. Malignant progression from adenoma of bronchiolar or alveolar origin to malignant tumors has been proposed to involve a stepwise transformation. In our study, adenomas developed into adenocarcinomas and large cell carcinomas after treatment with Fe-NTA. In contrast, after oral administration of propolis or artepillin C, adenomas did not progress to carcinomas. Instead of developing into large cell cancers, as induced by Fe-NTA in control mice, adenomas showed remarkable proliferation of macrophages and local anti-oxidant activity after treatment with either propolis or artepillin C. Propolis and artepillin C therefore appear to inhibit lipid peroxidation and the development of pulmonary cancers.

Ferric nitrilotriacetate Lipid peroxidation Pulmonary tumors Propolis Artepillin 

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Copyright information

© Springer-Verlag 2000

Authors and Affiliations

  • Tetsuo Kimoto
    • 1
  • Satomi Koya-Miyata
    • 1
  • Keiko Hino
    • 1
  • Mark  J. Micallef
    • 1
  • Toshiharu Hanaya
    • 1
  • Shigeyuki Arai
    • 1
  • Masao Ikeda
    • 1
  • Masashi Kurimoto
    • 1
  1. 1.Hayashibara Biochemical Laboratories Inc., Fujisaki Institute, Fujisaki 675-1, Okayama 702-8006, Japan

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