A low dose of aripiprazole attenuates the subject-rated effects of d-amphetamine
Abstract
Despite increased reports of amphetamine abuse and dependence, a putative pharmacotherapy has yet to be identified. In a previous study from our laboratory, 20 mg aripiprazole, an atypical antipsychotic that has partial agonist activity at D(2) receptors, attenuated many of the behavioral effects of d-amphetamine. Aripiprazole (20 mg) also impaired performance on a computerized version of the DSST when administered alone, indicating that the attenuation observed may have been functional as opposed to receptor mediated. The present experiment was conducted to determine whether a lower dose of aripiprazole (10 mg) could acutely attenuate the discriminative-stimulus, subject-rated, and physiological effects of d-amphetamine (2.5-15 mg) without impairing performance as measured with a computerized version of the DSST. The results of the present experiment indicate that 10 mg aripiprazole attenuated some abuse-related behavioral effects of d-amphetamine and was generally devoid of effects, including significant performance impairment, when administered alone. These findings suggest that 10 mg aripiprazole would be a reasonable starting dose for the treatment of stimulant abuse and dependence. Future research should examine the effects of chronic aripiprazole administration in combination with methamphetamine or cocaine.
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Risperidone has shown promise for the treatment of methamphetamine abuse, and aripiprazole is a promising treatment for amphetamine abuse.
“Finally, risperidone, a D2-receptor antagonist, has shown promise for the treatment of methamphetamine abuse [182], and aripiprizole, a partial D2 agonist is a promising treatment for amphetamine abuse [183].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [183]
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Self-citationRepeated aripiprazole administration attenuates cocaine seeking in a rat model of relapse
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InfluentialAripiprazole for Relapse Prevention and Craving in Alcohol-Dependent Subjects
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“…administered aripiprazole in non-treatment-seeking misusers of D-amphetamine or methamphetamine: acute aripiprazole reduced amphetamine’s discriminative-stimulus effects (Lile et al., 2005), positive subjective effects (Stoops et al., 2006), and rates of self-administration (Stoops et al., 2013).”
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“The dose of aripiprazole was selected because results of previous research indicates that 10 mg may be the lowest effective dose in terms of altering the behavioral effects of stimulants (6).”
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“…dosing procedures have demonstrated an attenuation of the effects of d-amphetamine in non-drug-dependent individuals (Lile et al., 2005; Stoops et al., 2006), whereas studies of repeated aripiprazole administration in dependent subjects have found enhanced effects for stimulants that…”
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“Given that 10 mg of aripiprazole appears to be the lower threshold of effective doses to alter the effects of stimulants such as cocaine and d-amphetamine (3, 20), aripiprazole might have a narrow therapeutic window as a pharmacotherapy for stimulant-use disorders.”
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“the atypical antipsychotic aripiprazole in combination with stimulant drugs have found that acute pretreatment attenuated the discriminative-stimulus and self-reported effects of cocaine and damphetamine (Lile et al., 2005, 2010; Stoops et al., 2006), but that the reinforcing and self-reported effects of cocaine were…”
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Attenuation of reinforcing and psychomotor stimulant effects of amphetamine by aripiprazole
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“Immediate administration of both low and high doses of aripiprazole has been shown to substantially attenuate the discriminative stimulus and subjective responses to amphetamine in humans.(45,47) However, several clinical studies involving a longer period of aripiprazole treatment have reported findings that are somew…”
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“Similarly, human laboratory studies show that ar-ipiprazole in doses ranging from 10 to 20mg reduces the reinforcing effects of amphetamine, cocaine, and methamphetamine (Lile et al., 2011; Stoops et al., 2006).”
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- Authors
- Stoops, W. W., Lile, J. A., Glaser, P. E. A., & Rush, C. R.
- Affiliations
- University of Kentucky (US)
- Corresponding author
- Rush, Craig R.
- Venue
- Drug and Alcohol Dependence
- Publisher
- Elsevier BV
- Published
- 2006-09
- Volume
- 84
- Issue
- 2
- Pages
- 206-209
- ISSN
- 0376-8716 (ISSN-L)
- OpenAlex
- W2045143875
- Cited by
- 57
- References
- 12
- Citations by year
- 2023: 2 · 2022: 2 · 2021: 1 · 2016: 3 · 2014: 1 · 2013: 2 · 2012: 5
- FWCI
- 3.42
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Drug and Alcohol Dependence (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Drug Abuse (R01 DA 010325, R01 DA 017711, T32 DA007304)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Keywords
- aripiprazole, d-amphetamine, stimulant abuse, stimulant use disorder, discriminative stimulus effects
- MeSH terms
- Aripiprazole, Adult, Central Nervous System Stimulants, Blood Pressure, Dextroamphetamine, Dose-Response Relationship, Drug, Drug Administration Schedule, Female, Heart Rate, Humans, Male, Piperazines, Surveys and Questionnaires, Antipsychotic Agents, Quinolones, Substance-Related Disorders
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