Expression of brain-derived neurotrophic factor, nerve growth factor, and heat shock protein HSP70 following fluid percussion brain injury in rats

Citation
J. Truettner et al., Expression of brain-derived neurotrophic factor, nerve growth factor, and heat shock protein HSP70 following fluid percussion brain injury in rats, J NEUROTRAU, 16(6), 1999, pp. 471-486
Citations number
84
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROTRAUMA
ISSN journal
08977151 → ACNP
Volume
16
Issue
6
Year of publication
1999
Pages
471 - 486
Database
ISI
SICI code
0897-7151(199906)16:6<471:EOBNFN>2.0.ZU;2-7
Abstract
Traumatic brain injury can induce the expression of stress-related and neur otrophic genes both within the injury site and in distant regions, These ge nes may affect severity of damage and/or be neuroprotective. We used in sit u hybridization to assess the alterations in expression of the heat shock p rotein HSP70, nerve growth factor (NGF), and brain-derived neurotrophic fac tor (BDNF) genes in rat brain following moderate fluid-percussion (F-P) inj ury at various survival times, HSP70 gene expression was induced at and sur rounding the injury site as early as 30 min after trauma, This elevated sig nal spread ventrally and laterally through the ipsilateral cortex and into the underlying white matter over the next few hours. In addition, there was elevated expression in the temporal hippocampus. BDNF was strongly upregul ated in the granular cells of the dentate gyrus and in the CA3 hippocampus 2-6 h after injury, Cortical regions at and near the injury site showed no response at the mRNA level. NGF mRNA increased over the granular cells of t he dentate gyrus at early time points, There was also a weaker secondary in duction of the NGF gene in the contralateral dentate gyrus of some animals, Cortical response was observed in the entorhinal cortex, bilaterally, but not at the injury site. All three of the studied genes responded quickly to injury, as early as 30 min, The induction of gene expression for neurotrop hins in regions remote from areas with histopathology may reflect coupling of gene expression to neuronal excitation, which may be associated with neu roprotection and plasticity.