Two strains of mice (NMRI and C57Bl/6) were treated with MPTP (within
8 h 4 x 30 mg/kg MPTP, IP) and motility was monitored 10 days later. A
n acute administration of amphetamine (25 mg/kg or 10.0 mg/kg) or apom
orphine (0.5 mg/kg or 5.0 mg/kg) led to hypermotility and a dose-depen
dent increase of stereotyped behavior. Immunocytochemical investigatio
ns indicated a substantial loss of tyrosine-hydroxylase immunoreactivi
ty in the basal ganglia which was accompanied by a 15% increase of H-3
-spiroperidol binding to a striatal membrane preparation. No differenc
e was found in biochemical and behavioral measures between both mice s
trains. Thus, MPTP-induced lesions in mice are probably followed by a
denervation-like supersensitivity of the dopaminergic system, which mi
ght account for the finding that despite a severe degeneration of dopa
minergic terminals amphetamine induces hypermotility. Copyright (C) 19
97 Elsevier Science Inc.