Neurotrophic factors appear to be crucial for the survival and potential
regeneration of injured neurons. Injury of the peripheral nervous system
results in the induction of a number of neurotrophic molecules. Less is
known about the response of central nervous tissue to injury. We have
examined levels of mRNA for three trophic factors, basic and acidic
fibroblast growth factor (bFGF, aFGF), and nerve growth factor (NGF),
after an incomplete thoracic contusive spinal cord injury (SCI). RNase
protection assays showed a rapid increase (three-fold) in the content of
bF6F mRNA by 6 hours that persisted for at least 7 days after SCI. The
induction of bFGF was specific, as no change in the levels of aFGF or NGF
mRNA were seen. These data support a speculative hypothesis that bFGF may
play a role in the partial recovery of function seen following incomplete
contusive spinal cord injury. We propose to test this hypothesis. We
will determine whether bFGF protein levels are also increased after SCI by
immunohistochemistry, Western blot analysis and proliferation assays.
Moreover, we will determine the location and cell types in which bFGF mRNA
and protein are induced with respect to the injury epicenter, by in situ
hybridization and immunohistochemistry. We will test specific hypotheses
that the induction of bFGF after SCI is important for a)
neovascularization, as well as b) neuronal survival and c) the glial
reaction, following SCI. We will investigate the potential
pharmacological manipulation of bFGF induction with corticosteroids, and
glutamate receptor antagonists, classes of drugs that have been shown
capable of enhancing functional recovery after traumatic SCI. These
studies offer promise in understanding the mechanisms leading to the
induction of bFGF in the CNS, as well as a potential new therapeutic
approach to SCI. On the basis of experimental and/or pharmacological
manipulation of bFGF levels, we will then rigorously test the hypothesis
that bFGF plays a significant role in the observed partial recovery of
sensori-motor function after SCI. Lastly, we will begin to place the
induction of bFGF in the context of the overall neurotrophic environment
in the spinal cord after injury. by initiating studies on the induction of
Brain. Derived Neurotrophic Factor (BDNF) after SCI. We expect that the
results from this project should provide important insights into natural,
endogenous, recovery mechanisms in the CNS that can in the future be
therapeutically manipulated.
National Institute of Neurological Disorders and Stroke
CFDA Code
DUNS Number
049515844
UEI
TF2CMKY1HMX9
Project Start Date
30-September-1994
Project End Date
31-August-1997
Budget Start Date
01-September-1995
Budget End Date
31-August-1996
Project Funding Information for 1995
Total Funding
$213,886
Direct Costs
$135,106
Indirect Costs
$78,780
Year
Funding IC
FY Total Cost by IC
1995
National Institute of Neurological Disorders and Stroke
$213,886
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01NS032671-02
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No Outcomes available for 5R01NS032671-02
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