Further evaluation of the reinforcing effects of the novel cocaine analog 2β-propanoyl-3β-(4-tolyl)-tropane (PTT) in rhesus monkeys

被引:20
|
作者
Birmingham, AM
Nader, SH
Grant, KA
Davies, HML
Nader, MA
机构
[1] Wake Forest Univ, Sch Med, Dept Physiol & Pharmacol, Ctr Neurobiol Invest Drug Abuse, Winston Salem, NC 27157 USA
[2] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
关键词
cocaine; tropanes; dopamine transporter; self-administration; rhesus monkey;
D O I
10.1007/s002130050549
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
2 beta-Propanoyl-3 beta-(4-tolyl)-tropane (PTT) is a cocaine analog which has been shown in rhesus monkeys to have cocaine-like discriminative stimulus effects and a long duration of action (>8 h), yet does not function as a reinforcer when substituted for cocaine in monkeys responding under a fixed-interval 5-min schedule (Nader et al. 1997). The purpose of the present study was to evaluate the reinforcing effects of PTT under a fixed-ratio (FR) schedule and to determine if decreasing the inter-injection interval would influence the reinforcing effects of PTT. Male rhesus monkeys (n=3) were trained to respond under a multiple FR 30 food-drug-food schedule. When responding was stable, cocaine (0.003-0.3 mg/kg per injection) or PTT (0.001-0.03 mg/kg per injection) was available during the drug component for at least five consecutive sessions and until stable responding was observed. To investigate whether the inter-injection interval would influence PTT-maintained response rates, the time-out (TO) following PTT injections was reduced from 180 or 300 s to 10 s for at least five consecutive sessions. Cocaine-maintained response rates were characterized as an inverted-U shaped function of dose, with peak rates maintained by 0.03 mg/kg per injection cocaine. PTT (0.001-0.03 mg/kg per injection) maintained response rates significantly higher than rates maintained by the PTT vehicle, but significantly lower than cocaine-maintained response rates; PTT intake increased with dose. A reduction of the TO following PTT injections to 10 s did not alter PTT-maintained response rates or total session intake. Self-administered PTT was more potent than cocaine at decreasing food-maintained responding. These results suggest that for long-acting compounds like PTT, reinforcing effects are more likely to be observed when the drug is available under a ratio-based schedule, compared to an interval-based schedule.
引用
收藏
页码:139 / 147
页数:9
相关论文
共 18 条
  • [1] Further evaluation of the reinforcing effects of the novel cocaine analog 2β-propanoyl-3β-(4-tolyl)-tropane (PTT) in rhesus monkeys
    Anne M. Birmingham
    Susan H. Nader
    Kathleen A. Grant
    Huw M. L. Davies
    Michael A. Nader
    Psychopharmacology, 1998, 136 : 139 - 147
  • [2] A comparison of the behavioral effects of the repeated administration of PTT, 2β-propanoyl-3β-(4-tolyl)tropane and cocaine
    Freedland, CS
    Smith, HR
    Hart, SL
    Daunais, JB
    Davies, HML
    Porrino, LJ
    BRAIN RESEARCH, 2000, 869 (1-2) : 98 - 104
  • [3] The reinforcing and discriminative stimulus effects of the novel cocaine analog 2 beta-propanoyl-3 beta-(4-tolyl)-tropane in rhesus monkeys
    Nader, MA
    Grant, KA
    Davies, HML
    Mach, RH
    Childers, SR
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 1997, 280 (02): : 541 - 550
  • [4] A cocaine analog, 2β-propanoyl-3β-(4-tolyl)-tropane (PTT), reduces tyrosine hydroxylase in the mesolimbic dopamine pathway
    Freeman, WM
    Yohrling, GJ
    Daunais, JB
    Gioia, L
    Hart, SL
    Porrino, LJ
    Davies, HML
    Vrana, KE
    DRUG AND ALCOHOL DEPENDENCE, 2000, 61 (01) : 15 - 21
  • [5] A novel cocaine analog, 2β-propanoyl-3β-(4-tolyl)-tropane (PTT) reduces tyrosine hydroxylase expression in the mesolimbic dopamine pathway.
    Freeman, WM
    Daunais, JB
    Gioia, L
    Porrino, LJ
    Davies, HML
    Vrana, KE
    JOURNAL OF NEUROCHEMISTRY, 1999, 72 : S22 - S22
  • [6] Effects of 2β-propanoyl-3β-(4-tolyl)-tropane (PTT) on the self-administration of cocaine, heroin, and cocaine/heroin combinations in rats
    Sizemore, GM
    Davies, HML
    Martin, TJ
    Smith, JE
    DRUG AND ALCOHOL DEPENDENCE, 2004, 73 (03) : 259 - 265
  • [7] First- versus last-session substitution:: An evaluation of the reinforcing effects of cocaine and the cocaine analogue 2β-propanoyl-3β-(4-tolyl)-tropane
    Lile, JA
    Morgan, D
    Nader, MA
    EXPERIMENTAL AND CLINICAL PSYCHOPHARMACOLOGY, 2000, 8 (03) : 424 - 433
  • [8] The reinforcing efficacy of the dopamine reuptake inhibitor 2β-propanoyl-3β-(4-tolyl)-tropane (PTT) as measured by a progressive-ratio schedule and a choice procedure in rhesus monkeys
    Lile, JA
    Morgan, D
    Birmingham, AM
    Wang, ZX
    Woolverton, WL
    Davies, HML
    Nader, MA
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 303 (02): : 640 - 648
  • [9] Characterization of a tropane radioligand, [3H]2β-propanoyl-3β-(4-tolyl) tropane ([3H]PTT), for dopamine transport sites in rat brain
    Letchworth, SR
    Smith, HR
    Porrino, LJ
    Bennett, BA
    Davies, HML
    Sexton, T
    Childers, SR
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2000, 293 (02): : 686 - 696
  • [10] BEHAVIORAL AND LOCAL CEREBRAL METABOLIC EFFECTS OF THE NOVEL TROPANE ANALOG, 2-BETA-PROPANOYL-3-BETA-(4-TOLYL)-TROPANE
    PORRINO, LJ
    DAVIES, HML
    CHILDERS, SR
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 1995, 272 (02): : 901 - 910