Characterization of the effects of bupropion on the reinforcing properties of nicotine and food in rats

被引:86
作者
Bruijnzeel, AW [1 ]
Markou, A [1 ]
机构
[1] Scripps Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
关键词
nicotine; self-administration; rat; bupropion; antidepressant; reward;
D O I
10.1002/syn.10242
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Bupropion is an atypical antidepressant drug that is the only nonnicotine-based prescription medicine approved for smoking cessation by the Food and Drug Administration. The aim of the present experiments was to investigate the effects of bupropion (5-40 mg/kg) on the reinforcing properties of nicotine and food in rats. The effects of bupropion were studied under two schedules of reinforcement: a fixed ratio 5 time-out 20-sec (FR5 TO20 s) and a progressive ratio (PR). Rats were trained to respond for nicotine (0.01 or 0.03 mg/kg/infusion, free base) or food under the FR5 TO20 s schedule. Pretreatment with the highest dose of bupropion (40 mg/kg) resulted in a significant reduction (similar to50%) of nicotine intake in rats self-administering 0.03 mg/kg/ infusion of nicotine. The same dose of bupropion also decreased (similar to40%) the self-administration of 0.01 mg/kg/infusion of nicotine, but this effect did not reach statistical significance. Pretreatment with bupropion slightly (similar to15%) reduced responding for food under the FR5 TO20 s schedule. Finally, pretreatment with bupropion did not affect the self-administration of nicotine (0.03 mg/kg/infusion) under a PR schedule, but dose-dependently increased responding for food under the same PR schedule. These findings indicate that a high dose of bupropion decreases the reinforcing properties of nicotine as measured under an FR schedule, while having no apparent effects on breaking points for nicotine under a PR schedule that reflects both the reinforcing properties and the motivation to obtain nicotine. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:20 / 28
页数:9
相关论文
共 67 条
[1]   Sustained-release bupropion smoking cessation in African Americans - A randomized controlled trial [J].
Ahluwalia, JS ;
Harris, KJ ;
Catley, D ;
Okuyemi, KS ;
Mayo, MS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (04) :468-474
[2]   A critique of fixed and progressive ratio schedules used to examine the neural substrates of drug reinforcement [J].
Arnold, JM ;
Roberts, DCS .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 57 (03) :441-447
[3]  
ASCHER JA, 1995, J CLIN PSYCHIAT, V56, P395
[4]   Nornicotine is self-administered intravenously by rats [J].
Bardo, MT ;
Green, TA ;
Crooks, PA ;
Dwoskin, LP .
PSYCHOPHARMACOLOGY, 1999, 146 (03) :290-296
[5]   Regional variation in the effects of nicotine on catecholamine overflow in rat brain [J].
Benwell, MEM ;
Balfour, DJK .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 325 (01) :13-20
[6]   EFFECT OF ACUTE ADMINISTRATION OF NICOTINE ON INVIVO RELEASE OF NORADRENALINE IN THE HIPPOCAMPUS OF FREELY MOVING RATS - A DOSE-RESPONSE AND ANTAGONIST STUDY [J].
BRAZELL, MP ;
MITCHELL, SN ;
GRAY, JA .
NEUROPHARMACOLOGY, 1991, 30 (08) :823-833
[7]  
Caine SB, 1993, BEHAV NEUROSCIENCE P, P117
[8]  
COOPER BR, 1980, J PHARMACOL EXP THER, V215, P127
[9]   Nucleus accumbens dopamine and work requirements on interval schedules [J].
Correa, M ;
Carlson, BB ;
Wisniecki, A ;
Salamone, JD .
BEHAVIOURAL BRAIN RESEARCH, 2002, 137 (1-2) :179-187
[10]   SELF-ADMINISTERED NICOTINE ACTIVATES THE MESOLIMBIC DOPAMINE SYSTEM THROUGH THE VENTRAL TEGMENTAL AREA [J].
CORRIGALL, WA ;
COEN, KM ;
ADAMSON, KL .
BRAIN RESEARCH, 1994, 653 (1-2) :278-284