The behavioral effects of L-dopa or cabergoline alone were compared with those of the joint administration of the two drugs in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-lesioned parkinsonian cynomolgus monkeys with attention to the induction of hyperactivity and dyskinesia. Cabergoline alone at 0.2mg/kg or less improved in a dose-dependent fashion the parkinsonism without inducing hyperactivity and dyskinesia following a single subcutaneous injection. L-dopa alone improved the parkinsonism, but induced hyperactivity and dyskinesia, depending on the dose applied. Doses required for 50% amelioration by L-dopa and cabergoline were 10 and 0.038mg/kg, s.c., respectively. With low doses (50%-amelioration doses), cabergoline or L-dopa alone improved the parkinsonism without induction of hyperactivity and dyskinesia, but the duration of action was brief. Cabergoline in combination with L-dopa was highly effective in improving motor disability without induction of hyperactivity and dyskinesia. Moreover, the duration of action was more prolonged with the coadministration than with the single administration of each drug. These findings suggest that the combined therapy with low doses of L-dopa and cabergoline is beneficial for treating patients with advanced Parkinson's disease.
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Kings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, EnglandKings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, England
Tel, BC
Cannizzaro, C
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Kings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, EnglandKings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, England
Cannizzaro, C
Pearce, RKB
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Kings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, EnglandKings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, England
Pearce, RKB
Rose, S
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Kings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, EnglandKings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, England
Rose, S
Jenner, P
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Kings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, EnglandKings Coll London, Jenner Neurodegenerat Dis Res Ctr, Pharmacol Grp, Div Biomed Sci, London SW3 6LX, England
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Univ London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, EnglandUniv London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, England
Maratos, E
Smith, L
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Univ London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, EnglandUniv London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, England
Smith, L
Jackson, MJ
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Univ London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, EnglandUniv London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, England
Jackson, MJ
Pearce, RKB
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Univ London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, EnglandUniv London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, England
Pearce, RKB
Jenner, P
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Univ London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, EnglandUniv London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, England
Jenner, P
Marsden, CD
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Univ London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, EnglandUniv London Kings Coll, Pharmacol Grp, Neurodegenerat Dis Res Ctr, London SW3 6LX, England