Genotoxic studies of vanadium pentoxide (V(2)O(5)) in male mice. II. Effects in several mouse tissues

Teratog Carcinog Mutagen. 1999;19(4):243-55. doi: 10.1002/(sici)1520-6866(1999)19:4<243::aid-tcm1>3.0.co;2-j.

Abstract

Vanadium pentoxide (V2O5) was tested for its ability to induce genotoxic damage in six different organs (liver, kidney, lung, spleen, heart, and bone marrow) of mice by using the alkaline Single Cell Gel Electrophoresis (SCGE) assay. Animals were sacrificed 24 h after i.p. administration of the vanadium pentoxide of 23.0, 11.5, or 5.75 microg/g (corresponding to the LD50, 1/2 LD50 and 1/4 LD50, respectively). In all tissues and organs evaluated (except for bone marrow), V2O5 increased the number of cells with damage. Our results showed that i.p. injection of V2O5 induced DNA damage in different organs and tissues, and that this kind of damage can be observed even 24 h after treatment. The analysis of DNA migration and the distribution of DNA damage showed that there are differences in sensitivity between organs and tissues to this compound. In addition the sensitivity of SCGE assay allows the detection of long term DNA damage and the possibility to compare it in various tissues and target organs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / pathology
  • Cell Survival / drug effects*
  • DNA Damage*
  • Dose-Response Relationship, Drug
  • Heart / drug effects
  • Kidney / cytology
  • Kidney / drug effects
  • Kidney / pathology
  • Liver / cytology
  • Liver / drug effects
  • Liver / pathology
  • Lung / cytology
  • Lung / drug effects
  • Lung / pathology
  • Male
  • Mice
  • Myocardium / cytology
  • Myocardium / pathology
  • Organ Specificity
  • Spleen / cytology
  • Spleen / drug effects
  • Spleen / pathology
  • Teratogens / toxicity*
  • Vanadium Compounds / toxicity*

Substances

  • Teratogens
  • Vanadium Compounds
  • vanadium pentoxide