Reactive oxygen species mediated tissue damage in high energy proton irradiated mouse brain

Mol Cell Biochem. 2012 Jan;360(1-2):189-95. doi: 10.1007/s11010-011-1056-2. Epub 2011 Sep 25.

Abstract

Although radiation related research has been conducted extensively, the molecular toxicology and cellular mechanisms affected by proton radiation remain poorly understood. We recently reported that the high energy protons induce cell death through activation of apoptotic signaling genes; caspase 3 and 8 (Baluchamy et al. J Biol Chem 285:24769-24774, 2010). In this study, we investigated the effect of different doses of protons in in vivo mouse system, particularly, brain tissues. A significant dose-dependent induction of reactive oxygen species and lipid peroxidation and reduction of antioxidants; glutathione and superoxide dismutase were observed in proton irradiated mouse brain as compared to control brain. Furthermore, histopathology studies on proton irradiated mouse brain showed significant tissue damage as compared to control brain. Together, our in vitro and in vivo results suggest that proton irradiation alters oxidant and antioxidant levels in the cells to cause proton mediated DNA/tissue damage followed by apoptotic cell death.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Brain / metabolism
  • Brain / pathology
  • Brain / radiation effects*
  • Glutathione / metabolism
  • Lipid Peroxidation / radiation effects
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Protons* / adverse effects
  • Radiation Injuries / metabolism*
  • Reactive Oxygen Species / metabolism*
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1

Substances

  • Antioxidants
  • Protons
  • Reactive Oxygen Species
  • Sod1 protein, mouse
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • superoxide dismutase 2
  • Glutathione