Neurotransmitter System | References | Type of Procedure; Training Drug; Training Dose (mg/kg/infusion); Schedule; Session Duration (h/day) | Discrete CS | Discriminative or Contextual Cues | Extinction Behavior |
---|---|---|---|---|---|
Cannabinoids | |||||
Cannabinoid antagonist: | |||||
SR141716A (0.3–3.0 mg/kg, s.c.) | De Vries et al., 2001 | B; C; 0.5; FR-5; 2 h | Attenuation | ||
Dopamine | |||||
D1-like receptor agonist: | |||||
SKF-81297 (1 mg/kg, s.c.) | Weiss et al., 2001 | B; C; 0.75; FR-1; 2 h | No effect | ||
D2-like receptor agonist: | |||||
PD 128,907 (0.3 mg/kg, s.c.) | Weiss et al., 2001 | B; C; 0.75; FR-1; 2 h | Attenuation | ||
D1-like receptor antagonist: | |||||
SCH-23390 (2 μg/side, BLA) | See et al., 2001 | B; 0.75; FR-1; 3 h | Attenuation | ||
SCH-23390 (1–10 μg/kg, s.c.) | Alleweireldt et al., 2002 | B; C; 0.75; VR-5; 2 h | Attenuation | ||
SCH-23390 (2.5–10 μg/kg, s.c.) | Ciccocioppo et al., 2001 | B; C; 0.75; FR-1; 2 h | Attenuation | ||
SCH-23390 (5–10 μg/kg, i.p.) | H. Crombag, J. W. Grimm, and Y. Shaham, submitted | B; C; 0.75; FR-1; 2 h | Attenuation | ||
SCH-39166 (10 μg/kg, s.c.) | Ciccocioppo et al., 2001 | B; C; 0.75; FR-1; 2 h | Attenuation | ||
SCH-39166 (10 μg/kg, s.c.) | Weiss et al., 2001 | B; C; 0.75; FR-1; 2 h | Attenuation | ||
D2-like receptor antagonist: | |||||
Raclopride (5 μg/side, BLA) | See et al., 2001 | B; 0.75; FR-1; 3 h | No effect | ||
Raclopride (50–100 μg/kg, i.p.) | Crombag et al., submitted | B; C; 0.75; FR-1; 2 h | Attenuation | ||
HAL (150–300 μg/kg, i.p.) | McFarland and Ettenberg, 1997 | B; H; runway; 0.1 | No effect | ||
D2/3 receptor antagonist: | |||||
Nafadotride (1 mg/kg, s.c.) | Weiss et al., 2001 | B; C; 0.75; FR-1; 2 h | Attenuation | ||
Glutamate | |||||
NMDA antagonist: | |||||
AP-5 (1.97 μg/side, BLA) | See et al., 2001 | B; 0.75; FR-1; 3 h | No effect | ||
D-CPPene (0.3–3 mg/kg, i.p.) | Bespalov et al., 2000 | B; 0.32; FR-1; 3 h | Attenuation | ||
Memantine (1–10 mg/kg, i.p.) | Bespalov et al., 2000 | B; 0.32; FR-1; 3 h | No effect | ||
Non-NMDA antagonist: | |||||
CNQX (0.83 μg/side, BLA) | See et al., 2001 | B; 0.75; FR-1; 3 h | No effect | ||
Noradrenaline | |||||
α2-Adrenoceptor agonist: | |||||
Lofexidine (100–200 mg/kg, i.p.) | Highfield et al., 2001 | B; 0.025 H+0.25 C; FR-1; 6 h | No effect | ||
Reuptake inhibitor: | |||||
DMI (10 mg/kg/day for 21 days, i.p.) | Fuchs et al., 1998 | B; 0.75; VR-5; 3 h | Attenuation | ||
Opioids | |||||
Antagonist: | |||||
Naloxone (0.5, 1, 3 mg/kg, i.p.) | McFarland and Ettenberg, 1998 | B; H; runway; 0.1 | No effect | ||
Serotonin | |||||
Reuptake inhibitor: | |||||
Fluoxetine (3.0 mg/kg/day for 20 days, i.p.) | Baker et al., 2001 | B; 0.5; FR-1; 6 h | Attenuation | ||
Tryptophan hydroxylase inhibitor: | |||||
Para-chlorophenylalanine (100 mg/kg 2 days, i.p.) | Tran-Nguyen et al., 1999 | B; 0.33; FR-1; 2 h | Attenuation | ||
Depletion of serotonin: | |||||
5,7-DHT (200 μg/20 μl, i.c.v.) | Tran-Nguyen et al., 2001 | B; 0.33; FR-1; 2–8 h | Attenuation |
Abbreviations: B, between-session reinstatement procedure; B-W, between-within session reinstatement procedure; C, cocaine; H, heroin; HAL, haloperidol; VR, variable ratio schedule of reinforcement; W, within-session reinstatement procedure.