In vitro and in vivo protective effects of granulocyte colony-stimulating factor against radiation-induced intestinal injury

Arch Pharm Res. 2013 Oct;36(10):1252-61. doi: 10.1007/s12272-013-0164-9. Epub 2013 Jun 1.

Abstract

Intestinal injury is a major cause of death after high-dose radiation exposure. The use of granulocyte-colony stimulating factor (G-CSF) to treat radiation injury has focused on enhancing recovery from hematopoietic radiation syndrome. We evaluated G-CSF for its ability to protect against radiation-induced intestinal injury in rat intestinal epithelial cells (IEC-6) and BALB/c mouse models. For in vitro tests, pre-radiation addition of G-CSF to IEC-6 prevented cytotoxicity and the loss of cell viability. Pre-radiation G-CSF treatment also reduced radiation-induced cleavage of caspase-3 and p53 in IEC-6. For in vivo tests, examination 12 h after abdominal irradiation showed that G-CSF-treated mice were protected against apoptosis of the jejunal crypts. G-CSF-treated mice also showed attenuated intestinal morphological changes 3.5 days after abdominal radiation (10 Gy). G-CSF also reduced the levels of proinflammatory cytokines interleukin-6 and tumor necrosis factor-α after radiation. This study showed that G-CSF may protect against radiation-induced intestinal damage through its anti-apoptotic and anti-inflammatory effects. These results suggest that G-CSF is promising candidate for protection against intestinal mucosal injury following irradiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Caspase 3 / metabolism
  • Cell Survival / drug effects
  • Granulocyte Colony-Stimulating Factor / pharmacology*
  • Interleukin-6 / metabolism
  • Jejunum / drug effects*
  • Jejunum / injuries
  • Jejunum / pathology
  • Male
  • Mice
  • Radiation Injuries, Experimental / blood
  • Radiation Injuries, Experimental / metabolism
  • Radiation Injuries, Experimental / pathology
  • Radiation Injuries, Experimental / prevention & control*
  • Radiation-Protective Agents / pharmacology*
  • Rats
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Interleukin-6
  • Radiation-Protective Agents
  • Tumor Necrosis Factor-alpha
  • Granulocyte Colony-Stimulating Factor
  • Caspase 3