The effect of implantation of carbon filaments and fetal tissues on the axo
nal regeneration following contusion injury in a rat model was investigated
by in situ immunofluorescence. Female Sprague-Dawley rats were subjected t
o severe contusion injury to the spinal cord at T-9-T-10. All animals were
divided into 5 groups (N = 5/group): normal controls, surgical controls, wi
th carbon filament implants, with fetal tissue implants and with implants c
onsisting of fetal tissue cocultured with carbon filaments. After a 10-week
survival period, the astroglial response was assessed by immunoreactive gl
ial fibrillary acidic protein and the neuro-axonal profile by immunoreactiv
e phosphorylated and nonphosphorylated neurofilament proteins. The contusio
n injury resulted in: (a) dramatically increased immunoreactivity of glial
fibrillary acidic protein indicating injury-associated reactive astrogliosi
s, (b) increase in immunoreactive phosphorylated neurofilament protein indi
cating upregulated phosphorylation of neurofilament protein, (c) with no ch
ange in the highly differentiated nonphosphorylated neurofilament protein w
hich normally occur in the nonregenerating mature neurons. Implantation of
fetal tissues alone following contusion injury did not show any appreciable
change with regard to the immunoreactivities for the glial and neuronal ma
rkers studied, compared to the injury controls. However, the implantation o
f carbon filaments alone or together with fetal tissues directed the growth
of glial fibrillary acidic protein-positive astroglia and phosphoneurofila
ment-positive neurites along the carbon fibers, with no effect on nonphosph
oneurofilament protein. In conclusion, implantation of carbon filaments app
ears to be critical for facilitating the attachment of astroglia forming a
substrate and scaffolding that can further support and direct the growth of
postlesional plastic axons across the lesion. In addition, carbon filament
prostheses in combination with fetal tissue implants provides an improved
combinational approach to promote regrowth of injured neurons following inj
ury. (C) 1999 Published by Elsevier Science Ltd on behalf of ISDN. All righ
ts reserved.