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Vol. 282, Issue 2, 834-838, 1997
Department of Pharmacology and Toxicology (A.E.F., R.R.M., J.W.G.,
G.R.H.) and
Center for Human Toxicology (D.G.W.), University of Utah,
Salt Lake City, Utah
Reactive oxygen species decrease dopamine transporter (DAT) function
in vitro. Because of this, and the finding that METH administration causes oxygen radical formation in vivo, the
effects of METH administration on DAT activity in rat striatum were
investigated. A single METH injection caused a dose-dependent (0-15
mg/kg) decrease in [3H]dopamine uptake into
striatal synaptosomes prepared 1 h after METH administration; an
effect attributable to a decreased Vmax of
[3H]dopamine uptake. Similarly, multiple
high-dose administrations of METH (10 mg/kg/dose; four doses at 2-h
intervals) decreased DAT function. The decreases in DAT activity after
either single or multiple METH administrations were reversed 24 h
after treatment. [3H]5HT transport into
striatal synaptosomes was also affected by METH treatment. Taken
together, these data suggest that METH decreases DAT activity, perhaps
through a reactive oxygen species-mediated mechanism. These findings
may have important implications regarding the role of oxidative events
in the physiological regulation of monoaminergic systems.
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