Blast wave exposure impairs memory and decreases axon initial segment length

J Neurotrauma. 2013 May 1;30(9):741-51. doi: 10.1089/neu.2012.2478. Epub 2013 Feb 6.


Exposure to a blast wave has been proposed to cause mild traumatic brain injury (mTBI), with symptoms including altered cognition, memory, and behavior. This idea, however, remains controversial, and the mechanisms of blast-induced brain injury remain unknown. To begin to resolve these questions, we constructed a simple compressed air shock tube, placed rats inside the tube, and exposed them to a highly reproducible and controlled blast wave. Consistent with the generation of a mild injury, 2 weeks after exposure to the blast, we found that motor performance was unaffected, and a panel of common injury markers showed little or no significant changes in expression in the cortex, corpus callosum, or hippocampus. Similarly, we were unable to detect elevated spectrin breakdown products in brains collected from blast-exposed rats. Using an object recognition task, however, we found that rats exposed to a blast wave spent significantly less time exploring a novel object when compared with control rats. Intriguingly, we also observed a significant shortening of the axon initial segment (AIS) in both the cortex and hippocampus of blast-exposed rats, suggesting altered neuronal excitability after exposure to a blast. A computational model showed that shortening the AIS increased both threshold and the interspike interval of repetitively firing neurons. These results support the conclusion that exposure to a single blast wave can lead to mTBI with accompanying cognitive impairment and subcellular changes in the molecular organization of neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / pathology*
  • Blast Injuries / complications
  • Blast Injuries / pathology*
  • Blast Injuries / physiopathology
  • Brain Concussion / complications*
  • Brain Concussion / pathology*
  • Brain Concussion / physiopathology
  • Computer Simulation
  • Disease Models, Animal
  • Fluorescent Antibody Technique
  • Immunoblotting
  • Male
  • Memory Disorders / etiology*
  • Memory Disorders / pathology
  • Memory Disorders / physiopathology
  • Models, Neurological
  • Rats
  • Rats, Sprague-Dawley