Persistence of genetic damage in mice exposed to low dose of X rays

Int J Radiat Biol. 2008 Mar;84(3):227-35. doi: 10.1080/09553000801902166.

Abstract

Purpose: The aim of this work was to evaluate the persistence of genetic damage in CBA/J mice treated with a single irradiation of 0.1 or 1 Gy of X rays.

Materials and methods: Peripheral blood was collected from irradiated and control mice after 30 min, 24 h, 7 days, 1, 3 and 6 months from exposure and analysed by comet assay. To investigate if the whole-body irradiation affect DNA repair, half of the sampled blood cells were in vitro-irradiated with additional 4 Gy and immediately analysed. Six months from exposure haematopoietic organs were sampled for measuring apoptotic index.

Results: In mice exposed to 1 Gy genetic damage was initially high and decreased during the experimental-time, while in the 0.1 Gy group damage, at first low, persisted and slightly increased. The 0.1 Gy-irradiated mice showed also a time-dependent increasing sensitivity to the in vitro-irradiation. Six months after whole-body irradiation, the percentage of apoptotic cells observed in haematopoietic compartments from 0.1 Gy-irradiated mice was significantly higher compared to controls and to 1 Gy mice.

Conclusions: Results demonstrated that a single exposure to low-dose might induce long-term damage. Persistence of genetic damage might have relevant implications for estimating risk for low doses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Blood Cells / pathology
  • Blood Cells / radiation effects
  • Bone Marrow / pathology
  • Bone Marrow / radiation effects
  • Comet Assay
  • DNA Damage*
  • Male
  • Mice
  • Mice, Inbred CBA
  • Oxidative Stress / radiation effects
  • Radiation Injuries, Experimental / etiology
  • Radiation Injuries, Experimental / pathology
  • Spleen / pathology
  • Spleen / radiation effects
  • Whole-Body Irradiation / adverse effects*