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Vol. 286, Issue 2, 688-696, August 1998
Unité de Neuropsychopharmacologie Expérimentale,
U.P.R.E.S.A. 6036 du C.N.R.S., Institut Fédératif de
Recherche Multidisciplinaire sur les Peptides, Faculté de
Médecine et Pharmacie de Rouen, Rouen, France
The conditioned place preference (CPP) induced by increasing doses
(1.25-40 mg/kg) of cocaine or the specific dopamine uptake inhibitor
GBR12783 was investigated in rats previously treated with cocaine (10 or 20 mg/kg), GBR12783 (10 mg/kg) or morphine (10 mg/kg) for 15 days.
In solvent-pretreated rats, cocaine- and GBR12783-induced CPPs were
biphasic, with the highest scores observed at 20 mg/kg. Prior exposure
to GBR12783 sensitized the rats to the rewarding effects of low doses
of either GBR12783 or cocaine. Pretreatment with cocaine 20 mg/kg, but
not 10 mg/kg, sensitized the rats to its own rewarding effects.
Furthermore, it was less efficient than GBR12783 in sensitizing the
animals to the rewarding effects of both drugs. These data confirm the
major role of dopamine uptake inhibition in the sensitization process.
On the other hand, the magnitude of CPP induced by a high dose of both
drugs (20 mg/kg) was decreased after pretreatment with either GBR12783
or cocaine, reaching the lower scores observed at 40 mg/kg. This decrease was unrelated to altered anxiety level but was associated with
sensitization to stereotypies. Morphine pretreatment modified neither
the CPP induced by high doses of cocaine or GBR12783 nor cocaine- or
GBR12783-induced stereotypies. However, prior exposure to morphine
sensitized the rats to the rewarding effects of cocaine (2.5 mg/kg) but
not to those of GBR12783, suggesting that other mechanisms working in
concert with dopamine may facilitate the rewarding effect of cocaine
without affecting that of GBR12783.
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