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Review
. 2008 Dec;16(6):458-74.
doi: 10.1037/a0014103.

Dual dopamine/serotonin releasers: potential treatment agents for stimulant addiction

Affiliations
Review

Dual dopamine/serotonin releasers: potential treatment agents for stimulant addiction

Richard B Rothman et al. Exp Clin Psychopharmacol. 2008 Dec.

Abstract

"Agonist therapy" for cocaine and methamphetamine addiction involves administration of stimulant-like medications (e.g., monoamine releasers) to reduce withdrawal symptoms and prevent relapse. A significant problem with this strategy is that many candidate medications possess abuse liability because of activation of mesolimbic dopamine (DA) neurons in the brain. One way to reduce DA-mediated abuse liability of candidate drugs is to add in serotonin (5-HT) releasing properties, since substantial evidence shows that 5-HT neurons provide an inhibitory influence over mesolimbic DA neurons. This article addresses several key issues related to the development of dual DA/5-HT releasers for the treatment of substance use disorders. First, the authors briefly summarize the evidence supporting a dual deficit in DA and 5-HT function during withdrawal from chronic cocaine or alcohol abuse. Second, the authors discuss data demonstrating that 5HT release can dampen DA-mediated stimulant effects, and the "antistimulant" role of 5-HT-sub(2C) receptors is considered. Next, the mechanisms underlying potential adverse effects of 5-HT releasers are described. Finally, the authors discuss recently published data with PAL-287, a novel nonamphetamine DA/5-HT releasing agent that suppresses cocaine self-administration but lacks positive reinforcing properties. It is concluded that DA/5-HT releasers could be useful therapeutic adjuncts for the treatment of cocaine and alcohol addictions, as well as for obesity, attention-deficit disorder, and depression.

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Figures

Figure 1
Figure 1
Chemical structures of stimulants discussed in this article.
Figure 2
Figure 2
The dual deficit model of stimulant addiction. According to the model, withdrawal from chronic stimulant use leads to decreased synaptic availability of dopamine (DA) and serotonin (5-HT). This dual deficit contributes to withdrawal symptoms, drug craving, and relapse. DA dysfunction underlies anhedonia and psychomotor disturbances, whereas 5-HT dysfunction causes depressed mood, obsessive thoughts, and lack of impulse control. Protracted withdrawal phenomena are postulated to contribute significantly to relapse. Taken from Rothman & Baumann (2003).
Figure 3
Figure 3
Acute effects of phentermine on rates of responding maintained under a fixed ratio (FR) 30 schedule of food (●) or cocaine (□) reinforcement. Different unit doses of intravenous cocaine, 10–100 μg/kg/injection, are indicated. Phentermine was administered intravenously. Effects on responding are mean ± SEM, expressed as percentage of individual control rates of responding for N = 3–4 monkeys. Control variability (filled symbols) is expressed as the average of individual coefficients of variation. Data taken from Wojnicki et al. (1999).
Figure 4
Figure 4
Effects of phentermine (3 mg/kg) and fenfluramine (0.3 mg/kg), given alone or in combination, on conditioned place preference. Conditioning score represents the mean difference between time (s) spent in the drug- versus vehicle-paired side of the test chamber. All drugs were administered intraperioneally. Each column represents the mean of N = 9–10 rats. *Significant place preference (Wilcoxon’s test, p < .05). Data taken from Rea et al. (1998).
Figure 5
Figure 5
Effects of acute fenfluramine administration on dialysate serotonin (5-HT) levels measured in blood from conscious rats previously treated with chronic administration of fenfluramine (A) or fluoxetine (B). For chronic treatments, drugs were dissolved in sterile saline (fenfluramine) or 50% ethanol/saline (fluoxetine), and administered subcutaneously via osmotic minipumps for 2 weeks. On the day of test, fenfluramine was dissolved in saline and administered intravenously at 0 min. Serial blood samples were withdrawn at 15-min intervals and immediately dialyzed. 5-HT levels are mean ± SEM for N = 9/group. * p < .05 compared with saline controls at corresponding time points (Duncans post hoc test). Data taken from Zolkowska et al. (2008).
Figure 6
Figure 6
Effects of high-dose administration of d-fenfluramine (dFEN) or m-chlorophenylpiperazine (mCPP) on postmortem tissue levels of serotonin (5-HT) and its metabolite 5-hydroxyindoleacetic acid (5-HIAA) in rat brain. dFEN or mCPP was administered ip at doses of 10 or 30 μmol/kg, every 2 h, for four doses. Rats were killed two weeks after the dosing regimen. Postmortem tissue levels of 5-HT and 5-HIAA in prefrontal cortex, nucleus accumbens, and caudate nucleus were determined by high-performance liquid chromatography with electrochemical detection (HPLC-ECD). These doses of dFEN and mCPP produce equivalent increases in extracellular 5-HT. Data are mean ± SEM, expressed as ng/mg protein for N = 4–6 rats/group. * p < .05 compared with saline-treated group (Duncan’s post hoc test). Data taken from Baumann et al. (2001).
Figure 7
Figure 7
Effects of PAL-287 on neurochemical and locomotor parameters in rats undergoing in vivo microdialysis in prefrontal cortex. Rats received intravenous injections of 1 mg/kg PAL-287 at time zero, followed by 3 mg/kg 60 min later. A, Concentrations of dopamine (DA) and serotonin (5-HT) in dialysate samples are mean ± SEM for N = 7 rats/group, expressed as % baseline. Baseline levels of DA and 5-HT were 0.43 ± 0.07 and 0.27 ± 0.06 pg/5 μl. B, Locomotor parameters are mean ± SEM for N = 7 rats/group, expressed as distance traveled in cm (ambulation) and number of repetitive movements (stereotypy). * p < .05 compared with preinjection control (Duncan’s post hoc test). Data taken from Rothman et al. (2005).
Figure 8
Figure 8
Effects of PAL-287 in the monkey self-administration assay. A, Self-administration of cocaine and PAL 287 by rhesus monkeys. Drugs were available under a fixed ratio (FR) 25 schedule of reinforcement for two hours/day. Each point is the mean of two sessions of access to each dose of the drugs. Data are mean ± SEM for N = 4 monkeys. Symbols without bars have variability smaller than the points. * p < .05 compared with saline-injected control (Newman–Keuls post hoc test). B, Effects of chronic 7-day treatment with PAL-287 on cocaine- and food-maintained responding. Control levels of responding were defined as levels of cocaine- or food-maintained responding observed during 7 days of saline treatment. Each point shows mean ± SEM for three monkeys, with data collected during the last three days of each 7-day treatment. *p < .05 compared with control for a given reinforcer (Newman–Keuls). ¥ p < .05 compared with cocaine-maintained responding at that dose of PAL-287 (Newman–Keuls). Data taken from Rothman et al. (2005).

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