Activation of alpha 7 nicotinic acetylcholine receptor protects mice from radiation-induced intestinal injury and mortality

Radiat Res. 2014 Jun;181(6):666-71. doi: 10.1667/RR13575.1. Epub 2014 May 14.

Abstract

Radiation-induced gastrointestinal syndrome occurs when the body is exposed to a high dose of radiation. Currently, safe and effective radioprotectants are not available. Apoptosis was reported to play a primary role in radiation-induced injury. Recent evidence suggests that stimulation of α7 nicotinic acetylcholine receptor (α7nAChR) prevents cell death by inhibition of apoptosis. In this study, we demonstrated that a single dose of PNU282987 (100 μg/kg, i.p.), a selective α7nAChR agonist, protected mice from intestinal injury and significantly improved survival when administered prior to lethal 8 Gy total body irradiation. In vitro, PNU282987 protected against 8 Gy radiation-induced cell death in human umbilical venous endothelial cells by inhibiting apoptosis. We conclude that activation of α7nAChR may provide a new therapeutic pathway for the treatment of radiation-induced damage and mortality.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / radiation effects
  • Gene Expression Regulation / radiation effects
  • Humans
  • Intestines / drug effects
  • Intestines / radiation effects*
  • Male
  • Mice
  • Radiation Injuries / drug therapy*
  • Radiation Injuries / genetics
  • Radiation Injuries / metabolism*
  • Whole-Body Irradiation
  • Wounds and Injuries / metabolism*
  • Wounds and Injuries / pathology
  • alpha7 Nicotinic Acetylcholine Receptor / biosynthesis
  • alpha7 Nicotinic Acetylcholine Receptor / genetics*

Substances

  • alpha7 Nicotinic Acetylcholine Receptor