Neuroimplantation is inevitably accompanied by gliosis. Although graft
-induced trophic effects on host neurons may be mediated by glial cell
s, the effects of gliosis on dopamine (DA) metabolism remains unclear.
To examine these effects, basic fibroblast growth factor (bFGF) was d
irectly infused into the striatum of 12 male rats (250-280 g). One wee
k later, substantial gliosis was demonstrated in the infused striatum
by immunochemical staining for glial fibrillary acidic protein (GFAP)
and quantified by GFAP Western blot analysis. One week after bFGF infu
sion, estracellular DA and its metabolites were measured by in vivo mi
crodialysis using HPLC. Infusion of L-DOPA through the dialysis probe
resulted in a 60% reduction in the L-DOPA-induced DA peak in the gliot
ic striatum compared with the normal side. After L-DOPA infusion, dihy
droxyphenylacetic acid (DOPAC) levels were similar between the gliotic
and normal striatum. In contrast, homovanillic acid (HVA) levels were
26% higher in the gliotic striatum. Enzyme assays demonstrated that a
romatic L-amino acid decarboxylase activity was unchanged in the gliot
ic striatum, but both MAO-A and MAO-B activities increased by 23% and
21%, respectively. These results suggest that the reduced striatal DA
peak in the gliotic striatum after L-DOPA administration was due to ac
celerated DA catabolism through enhanced MAO activity. The bFGF-induce
d striatal gliosis may serve as a model to study neurotransmitter meta
bolism in the gliotic brain caused by disease processes, aging, or tis
sue grafting.