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Effects of drug history on the acquisition of responding maintained by GBR 12909 in rhesus monkeys

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Abstract

The reinforcing effects of cocaine have been associated with its actions at the dopamine reuptake site. Previous studies have shown that selective dopamine reuptake inhibitors can attenuate cocaine self-administration in animals, suggesting that they may serve as pharmacotherapeutic agents. In order to assess the potential reinforcing effects of one of these agents, the acquisition and maintenance of GBR 12909 self-administration were studied in different groups of rhesus monkeys (Macaca mulatta) that were either experimentally naive or experienced with respect to the self-administration of cocaine or GBR 12909. Lever-pressing was maintained under a multiple FR30 schedule with alternating components of either food or drug presentation. Experimentally naive monkeys failed to self-administer low doses of GBR 12909 (3–30 µg/kg per injection). However, after a history of cocaine self-administration, GBR 12909 (56 µg/kg per injection and then 30 µg/kg per injection) maintained numbers of drug deliveries similar to those maintained by cocaine. When another group of experimentally-naive monkeys was initially exposed to GBR 12909 self-administration, 56 µg/kg per injection failed to maintain responding. However, subsequent exposure to 100 µg/kg per injection established GBR 12909 self-administration, and high levels of responding were sustained later when the unit dose was decreased to 30 µg/kg per injection. In monkeys with prior experience with cocaine self-administration (∼75 sessions) unit doses of either 30 µg/kg per injection or 56 µg/kg per injection GBR 12909 maintained responding. In another group of monkeys with a more extensive history of cocaine self-administration (∼320 sessions), unit doses of either 10 µg/kg per injection or 30 µg/kg per injection GBR 12909 maintained responding. These results show that drug-maintained responding can be established with higher unit doses of GBR 12909. After exposure to these higher, more effective doses of GBR 12909, or effective doses of cocaine, lower doses of GBR 12909 are more likely to support drug-maintained responding.

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References

  • Andersen PH (1987) Biochemical and pharmacological characterization of [3H]GBR 12935 binding in vitro to rat striatal membranes: labelling of the dopamine uptake complex. J Neurochem 48:1887–1896

    Google Scholar 

  • Andersen PH (1989) The dopamine uptake inhibitor GBR 12909: selectivity and molecular mechanism of action. Eur J Pharmacol 166:493–504

    Google Scholar 

  • Baldo BA, Kelley AE (1991) Cross-sensitization between cocaine and GBR 12909, a dopamine uptake inhibitor. Brain Res Bull 27:105–108

    Google Scholar 

  • Balster RL, Schuster CR (1973) Fixed-interval schedule of cocaine reinforcement: effect of dose and infusion duration. J Exp Anal Behav 20:119–129

    Google Scholar 

  • Beardsley PM, Hayes BA, Balster RL (1990) The self-administration of MK-801 can depend upon drug-reinforcement history, and its discriminative stimulus properties are phencyclidinelike in rhesus monkeys. J Pharmacol Exp Ther 252:953–959

    Google Scholar 

  • Bergman J, Madras BK, Johnson SE, Spealman RD (1989) Effects of cocaine and related drugs in nonhuman primates. III Selfadministration by squirrel monkeys. J Pharmacol Exp Ther 251:150–155

    Google Scholar 

  • Cunningham KA, Callahan PM (1991) Monoamine reuptake inhibitors enhance the discriminative state induced by cocaine in the rat. Psychopharmacology 104:177–180

    Google Scholar 

  • Downs DA, Woods JH (1974) Codeine- and cocaine-reinforced responding in rhesus monkeys: effects of dose on response rates under a fixed-ratio schedule. J Pharmacol Exp Ther 191:179–188

    Google Scholar 

  • Gawin FH (1988) Chronic neuropharmacology of cocaine: progress in pharmacotherapy. J Clin Psychiat 49:11–16

    Google Scholar 

  • Glowa JR, Wojnicki FHE, Matecka D, Bacher JD, Mansbach RS, Balster RL, Rice KC (1995a) Effects of dopamine reuptake inhibitors on food and cocaine maintained responding. I: Dependence on unit dose of cocaine. Exp Clin Psychopharmacol 3:219–231

    Google Scholar 

  • Glowa JR, Wojnicki FHE, Matecka D, Rice KC, Rothman RB (1995b) Effects of dopamine reuptake inhibitors on food and cocaine maintained responding: II: Comparisons with other drugs and repeated administrations. Exp Clin Psychopharmacol 3:232–239

    Google Scholar 

  • Goldberg S (1973) Comparable behavior maintained under fixedratio and second-order schedules of food presentation, cocaine injection ord-amphetamine injection in the squirrel monkey. J Pharmacol Exp Ther 186:18–30

    Google Scholar 

  • Heikkila RE, Manzino L (1984) Behavioral properties of GBR 12909, GBR 13069, and GBR 13098: specific inhibitors of dopamine uptake. Eur J Pharmacol 103:241–248

    Google Scholar 

  • Henningfield JE, Keenan RM (1993) Nicotine delivery kinetics and abuse liability. J Consult Clin Psychol 61:743–750

    Google Scholar 

  • Horger BA, Shelton K, Schenk S (1990) Preexposure sensitizes rats to the rewarding effects of cocaine. Pharmacol Biochem Behav 37:707–711

    Google Scholar 

  • Horger BA, Wellman PJ, Morien A, Davies BT, Schenk S (1991) Caffeine exposure sensitizes rats to the reinforcing effects of cocaine. Neuroreport 2:53–26

    Google Scholar 

  • Howell LL, Byrd LD (1991) Characterization of the effects of cocaine and GBR 12909, a dopamine uptake inhibitor, on behavior in the squirrel monkey. J Pharmacol Exp Ther 258:178–185

    Google Scholar 

  • Kelly AE, Lang CG (1989) Effects of GBR 12909, a selective dopamine uptake inhibitor, on motor activity and operant behavior in the rat. Eur J Pharmacol 167:385–395

    Google Scholar 

  • Kleven MS, Anthony EW, Woolverton WL (1988) Reinforcing and discriminative stimulus effects of GBR12909 in rhesus monkeys. Neurosci Abstr 1:305

    Google Scholar 

  • Kleven MS, Anthony EW, Woolverton WL (1990) Pharmacological characterization of the discriminative stimulus effects of cocaine in rhesus monkeys. J Pharmacol Exp Ther 254:312–317

    Google Scholar 

  • Melia KF, Spealman RD (1991) Pharmacological characterization of the discriminative-stimulus effects of GBR 12909. J Pharmacol Exp Ther 258:626–632

    Google Scholar 

  • Piazza PV, Deminiere J, LeMoal M, Simon H (1989) Factors that predict individual vulnerability to amphetamine self-administration. Science 245:1511–1513

    Google Scholar 

  • Piazza PV, Deminiere J, LeMoal M, Simon H (1990) Stress-and pharmacologically-induced behavioral sensitization increases vulnerability to acquisition of amphetamine self-administration. Brain Res 514:22–26

    Google Scholar 

  • Reith ME, Sershen H, Lajtha A (1981) Binding of [3H]cocaine in mouse brain: kinetics and saturability. J Recept Res 2:233–243

    Google Scholar 

  • Ritz MC, Lamb RJ, Goldberg SR, Kuhar MJ (1987) Cocaine receptors on dopamine transporters are related to self-administration of cocaine. Science 237:1219–1223

    Google Scholar 

  • Roberts DC (1993) Self-administration of GBR 12909 on a fixed ratio and progressive ratio schedule in rats. Psychopharmacology 111:202–206

    Google Scholar 

  • Robinson TE, Berridge KC (1993) The neural basis of drug craving: an incentive-sensitization theory of addiction. Brain Res Rev 18:247–291

    Google Scholar 

  • Rothman RB (1990) High affinity dopamine reuptake inhibitors as potential cocaine antagonists: a strategy for drug development. Life Sci 46:PL17–21

    Google Scholar 

  • Rothman RB, Grieg N, Kim A, de Costa BR, Rice KC, Carroll FI, Pert A (1992) Cocaine and GBR 12909 produce equivalent motoric responses at different occupancy of the dopamine transporter. Pharmacol Biochem Behav 43:1135–1142

    Google Scholar 

  • Skjoldager P, Winger G, Woods JH (1993) Effects of GBR 12909 and cocaine on cocaine-maintained behavior in rhesus monkeys. Drug Alcohol Depend 33:31–39

    Google Scholar 

  • Spealman RD (1993) Modification of behavioral effects of cocaine by selective serotonin and dopamine uptake inhibitors in squirrel monkeys. Psychopharmacology 112:93–99

    Google Scholar 

  • Spealman RD, Madras BK, Bergman JS (1989) Effects of cocaine and related drugs in nonhuman primates. II. Stimulant effects on schedule-controlled behavior. J Pharmacol Exp Ther 251:142–149

    Google Scholar 

  • Valadez A, Schenk S (1994) Persistence of the ability of amphetamine preexposure to facilitate acquisition of cocaine self-administration. Pharmacol Biochem Behav 47:203–205

    Google Scholar 

  • Van der Zee P, Koger HS, Gootjes J, Hespe W (1980) Aryl 1,4 dialk(en)yl-piperazines as selective and very potent inhibitors of dopamine uptake. Eur J Med Chem 15:363–370

    Google Scholar 

  • Witkin JM, Nichols DE, Terry P, Katz JL (1991) Behavioral effects of selective dopaminergic compounds in rats discriminating cocaine injections. J Pharmacol Exp Ther 257:706–713

    Google Scholar 

  • Wojnicki FHE, Bacher JB, Glowa JR (1994) Use of subcutaneous vascular access ports in rhesus monkeys. Lab Anim Sci 44:491–494

    Google Scholar 

  • Woolverton WL, Cervo L, Johanson CE (1984) Effects of repeated methamphetamine administration on methamphetamine self-administration in rhesus monkeys. Pharmacol Biochem Behav 21:737–741

    Google Scholar 

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Wojnicki, F.H.E., Glowa, J.R. Effects of drug history on the acquisition of responding maintained by GBR 12909 in rhesus monkeys. Psychopharmacology 123, 34–41 (1996). https://doi.org/10.1007/BF02246278

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  • DOI: https://doi.org/10.1007/BF02246278

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