Skip to main navigation Skip to search Skip to main content

Topical and oral administration of the natural water-soluble antioxidant from spinach reduces the multiplicity of papillomas in the Tg.AC mouse model

  • Abraham Nyska
  • , Liat Lomnitski
  • , Judson Spalding
  • , David B. Dunson
  • , Thomas L. Goldsworthy
  • , Shlomo Grossman
  • , Margalit Bergman
  • , Gary Boorman
  • National Institutes of Health
  • ILS, Inc.
  • Bar-Ilan University

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

The Tg.AC mouse carrying the v-Ha-ras structural gene is a useful model for the study of chemical carcinogens, especially those acting via non-genotoxic mechanisms. This study evaluated the efficacy of the non-toxic, water-soluble antioxidant from spinach, natural antioxidant (NAO), in reducing skin papilloma induction in female hemizygous Tg.AC mice treated dermally five times over 2.5 weeks with 2.5 μg 12-O-tetradecanoylphorbol-13-acetate (TPA). The TPA-only group was considered as a control; the other two groups received, additionally, NAO topically (2 mg) or orally (100 mg/kg), 5 days/week for 5 weeks. Papilloma counts made macroscopically during the clinical observations showed a significant decrease in multiplicity (P < 0.01) in the NAO topically treated group. According to histological criteria, papilloma multiplicity were lower in both topical-NAO and oral-NAO groups, but significantly so only in the oral-NAO mice (P < 0.01). The beneficial effect of NAO in the Tg.AC mouse is reported.

Original languageEnglish
Pages (from-to)33-44
Number of pages12
JournalToxicology Letters
Volume122
Issue number1
DOIs
StatePublished - 31 May 2001

Funding

FundersFunder number
National Institute of Environmental Health SciencesZ01ES040009

    Keywords

    • Natural antioxidant
    • Papilloma
    • Skin
    • Tg.AC mouse
    • Transgenic

    Fingerprint

    Dive into the research topics of 'Topical and oral administration of the natural water-soluble antioxidant from spinach reduces the multiplicity of papillomas in the Tg.AC mouse model'. Together they form a unique fingerprint.

    Cite this