EFFECTS OF GLIOSIS ON DOPAMINE METABOLISM IN RAT STRIATUM

Citation
J. Wang et al., EFFECTS OF GLIOSIS ON DOPAMINE METABOLISM IN RAT STRIATUM, Brain research, 663(2), 1994, pp. 199-205
Citations number
30
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00068993
Volume
663
Issue
2
Year of publication
1994
Pages
199 - 205
Database
ISI
SICI code
0006-8993(1994)663:2<199:EOGODM>2.0.ZU;2-G
Abstract
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.