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The Journal of Neuroscience, March 1, 2000, 20(5):1849-1857
Activation of Extracellular Signal-Regulated Protein Kinases Is
Associated with a Sensitized Locomotor Response to D2
Dopamine Receptor Stimulation in Unilateral
6-Hydroxydopamine-Lesioned Rats
Guoping
Cai,
Xuechu
Zhen,
Kunihiro
Uryu, and
Eitan
Friedman
Laboratory of Molecular Pharmacology, Department of Pharmacology
and Physiology, MCP Hahnemann School of Medicine, Philadelphia,
Pennsylvania 19129
Evidence indicates that mitogen-activated protein kinase
(MAPK) pathways play a crucial role in the neurobiology of the nervous system. In the present study, dopamine receptor-mediated regulation of
extracellular signal-regulated kinases (ERKs) was examined in rats in
which the nigrostriatal dopaminergic pathway was unilaterally lesioned
by 6-hydroxydopamine (6-OHDA). Subcutaneous injections of the
D2 receptor agonist quinpirole significantly increased tyrosine-phosphorylated ERK1/2 in lesioned striatum, whereas the D1 receptor agonist SKF38393 failed to activate ERKs.
Quinpirole-induced phosphorylation of ERK1/2 was seen as early as 3 min
and peaked at 15 min after the challenge. In parallel, striatal ERK
kinase activity, measured by the in vitro kinase assay,
was increased 2.5-fold on the lesioned side after the administration of
quinpirole. Immunohistochemical examination of brain sections after
quinpirole administration revealed significant increases in ERK1/2
immunostaining in perinuclear and intranuclear areas of striatal
neurons. This increase was much more pronounced on the lesioned than
the intact side. Furthermore, quinpirole-induced contralateral rotation
was decreased by 48.7 and 50.7%, respectively, when the striatal ERK pathway was selectively inhibited by a single intrastriatal injection of the MAPK/ERK kinase inhibitor PD098059 or after a continuous 7 d intrastriatal infusion of ERK1/2 antisense oligodeoxynucleotide. The
results demonstrate, for the first time, that the ERK signaling pathway
is activated in denervated striatum in response to stimulation of
D2 dopamine receptors and that the resulting imbalance in
striatal ERK activity contributes, at least in part, to neuronal
plasticity that underlies D2 dopamine receptor-mediated
contralateral rotation in unilateral 6-OHDA denervated rats.
Key words:
Dopamine receptor; supersensitivity; ERK pathway; locomotion; phosphorylation; striatum
Copyright © 2000 Society for Neuroscience 0270-6474/00/2051849-09$05.00/0
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