In this study, we evaluated whether enhancement of the serotonin tone induced by the administration of the serotonin precursor 5-hydroxy-tryptophan (5-HTP) could affect induction and expression of LID, as well as the therapeutic effect of l-DOPA, in 6-OHDA-lesioned rats.
Drug na?ve and l-DOPA-primed 6-OHDA-lesioned rats were chronically treated with a daily injection of l-DOPA (6 mg/kg plus benserazide, s.c.) alone, or in combination with 5-HTP (24-48 mg/kg, i.p.). The abnormal involuntary movements (AIMs) test, as well as the stepping and the motor activity tests, were performed during the chronic treatments.
Results showed that 5-HTP reduced the appearance of LID of about 50 % at both tested doses. A partial reduction of the therapeutic effect of l-DOPA was seen with the higher but not with the lower dose of 5-HTP. 5-HTP 24 mg/kg was also able to reduce the expression of dyskinesia in l-DOPA-primed dyskinetic rats, to a similar extent than in l-DOPA-primed rats.
Importantly, the antidyskinetic effect of 5-HTP 24 mg/kg does not appear to be due to a competition with l-DOPA for crossing the blood-brain barrier; in fact, similar l-DOPA striatal levels were found in l-DOPA only and l-DOPA plus 5-HTP 24 mg/kg treated animals. These data further confirm the involvement of the serotonin system in the appearance of LID, and suggest that 5-HTP may be useful to counteract the appearance of dyskinesia in Parkinson's disease patients.