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Departamento de Bioquímica, Bromatología y
Toxicología, Facultad de Farmacia, Universidad de Sevilla,
41012-Sevilla, Spain
We have studied the effect of chronic treatment with nomifensine on
dopaminergic functioning in the nigrostriatal system. The striatal
dopaminergic system was not altered by chronic nomifensine treatment.
In contrast, there were overall decreases of different dopamine (DA)
metabolites in the cell body region in the substantia nigra after
nomifensine treatment, which clearly indicates a diminished DA
turnover. These results suggest that long-lasting inhibition of the
high affinity DA uptake system triggers long term regulatory, compensatory mechanisms in the cell body region to preserve normal dopaminergic function in the terminal field in striatum. We also tested
whether transcriptional regulatory mechanisms were altered. We studied
the cellular expression of tyrosine hydroxylase (TH) mRNA in substantia
nigra by in situ hybridization, and the amount and
activity of TH enzyme in the cell body and terminal field regions. Our
results indicate that nomifensine treatment increased TH mRNA levels
within individual nigral cells, which paralleled the changes in TH
enzyme amount and activity in this brain area. Our data confirm the
important role of the high affinity DA uptake system in regulating
dopaminergic transmission in the nigrostriatal system.