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Systemic administration of 1<i>R,</i>4<i>S</i>‐4‐amino‐cyclopent‐2‐ene‐carboxylic acid, a reversible inhibitor of GABA transaminase, blocks expression of conditioned place preference to cocaine and nicotine in rats
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Citations
18
References
2002
Year
Behavioral AddictionPsychopharmacologyPharmacotherapyExperimental PharmacologySocial SciencesMolecular PharmacologyReversible InhibitionNicotineAddiction MedicineGaba TransaminaseSystemic AdministrationPsychoactive DrugReversible InhibitorNeuropharmacologyPharmacologyInhibitory NeurotransmittersSubstance AbuseAddictionPhysiologyNeuroscienceMedicineConditioned Place Preference
We examined the effect of 1R,4S-4-amino-cyclopent-2-ene-carboxylic acid (ACC), a reversible inhibitor of GABA transaminase, on the expression of conditioned place preference response to cocaine and nicotine in rats. Cocaine (20 mg/kg i.p.) and nicotine (0.4 mg/kg s.c.), but not vehicle or 300 mg/kg i.p. of ACC, produced a significant conditioned place preference response. Pretreatment of animals with 300 and 75 mg/kg i.p. of ACC significantly attenuated the expression of the cocaine- and nicotine-induced conditioned place preference responses, respectively. These results are the first to suggest that reversible inhibition of GABA transaminase may be useful in blocking cue-induced relapse to nicotine and cocaine.
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