Molecular correlates of age-specific responses to traumatic brain injury in mice

Syed A. Shah, Donald S. Prough, Jeanna M. Garcia, Douglas S. DeWitt, Helen Hellmich

Research output: Contribution to journalArticlepeer-review

28 Scopus citations


Aged traumatic brain injury (TBI) patients suffer higher rates of mortality and disability than younger patients. Cognitive problems common to TBI patients are associated with damage to the hippocampus, a central locus of learning and memory. To investigate the molecular mechanisms of age-related vulnerability to brain injury in a mouse model of TBI, we studied the effects of TBI on hippocampal gene expression in young and aged mice. Young and aged male C57Bl/6 mice were subjected to sham injury or TBI and sacrificed 24 h post-injury. We used laser capture microdissection to obtain pure populations of neurons from the CA1, CA3, and dentate gyrus subfields of the hippocampus. We compared injury-induced gene expression in hippocampal neurons of young and aged mice using quantitative ribonuclease protection assay analysis of linearly amplified mRNA from laser captured neurons. Both increased age and TBI were associated with increased expression of neuroprotective (brain-derived neurotrophic factor), pro-inflammatory (interleukin-1β), and proapoptotic (caspase-3) genes in mouse hippocampal neurons. Our data support previous reports that suggested the CA3 subregion is highly susceptible to fluid percussion TBI and that age-related changes in gene expression are one potential mechanism of increased vulnerability of the aged brain to TBI.

Original languageEnglish (US)
Pages (from-to)1201-1205
Number of pages5
JournalExperimental Gerontology
Issue number11
StatePublished - Nov 2006


  • Brain-derived neurotrophic factor
  • Caspase-3
  • Fluid percussion TBI
  • Interleukin-1β
  • Ribonuclease protection assay

ASJC Scopus subject areas

  • Biochemistry
  • Aging
  • Molecular Biology
  • Genetics
  • Endocrinology
  • Cell Biology


Dive into the research topics of 'Molecular correlates of age-specific responses to traumatic brain injury in mice'. Together they form a unique fingerprint.

Cite this