Can Cocaine Craving Be a Medication Development Outcome?: Drug Craving and Relapse in Opioid and Cocaine Dependence

1992 ◽  
Vol 1 (3) ◽  
pp. 230-239 ◽  
Author(s):  
Thomas R. Kosten
2013 ◽  
Vol 38 (9) ◽  
pp. 1532-1544 ◽  
Author(s):  
Helen C. Fox ◽  
Mehmet Sofuoglu ◽  
Peter T. Morgan ◽  
Keri L. Tuit ◽  
Rajita Sinha

2021 ◽  

Goals: Non-systematic literature review of the role of aripiprazole in alleviating cocaine craving in schizophrenic patients with cocaine-dependence (CD). Material and methods: From the review performed, 2 studies outstand: In one study, 6 schizophrenic patients with CD completed 8 weeks of treatment with aripiprazole at a maximum dose of 15 mg/d. The Brief Psychiatric Rating Scale and the Brief Substance Craving Scale (BSCS) were used to measure psychosis and subjective cocaine and alcohol cravings and urine tests for cocaine were performed. In another study, 44 CD patients with schizophrenia or schizoaffective disorder were treated with aripiprazole or perphenazine during 8 weeks. The perphenazine group received the recommended dosage not exceeding 24 mg/d and the patients receiving aripripazole were started on 15 mg/d to a maximum of 30 mg/d or a minimum of 10 mg/d. Primary outcome targeted cocaine-free urine sample proportions, whereas secondary outcome focused on cocaine craving scores. BSCS was used to assess cocaine craving and the positive and negative symptom scale and the clinical global impression scale were used to monitor psychotic symptom severities. Results and conclusion: In the first study, positive urine tests dropped significantly after 2 weeks, mean cocaine and acohol craving scores declined significantly, and declining psychosis scores were associated with declining cocaine and alcohol craving. In the second study, the proportion of negative drug test results did not differ significantly between patients treated with aripiprazol or perphenazine. Regarding the anticraving effect, in the aripiprazol group during week 3 to 8, significant reductions in craving intensity, frequency and duration were seen, while no similar reduction was seen with perphenazine. In conclusion, although the results are still limited, studies suggest that aripiprazol may have a potential effect in dual diagnosis patients with schizophrenia and CD, possibly due to its dopamine activity as a partial agonist/antagonist.


2012 ◽  
Vol 169 (4) ◽  
pp. 406-414 ◽  
Author(s):  
Marc N. Potenza ◽  
Kwang-ik Adam Hong ◽  
Cheryl M. Lacadie ◽  
Robert K. Fulbright ◽  
Keri L. Tuit ◽  
...  

2021 ◽  
Author(s):  
Céline Nicolas ◽  
Natalie E. Zlebnik ◽  
Mehdi Farokhnia ◽  
Lorenzo Leggio ◽  
Satoshi Ikemoto ◽  
...  

AbstractA widely held dogma in the preclinical addiction field is that females are more vulnerable than males to drug craving and relapse. Here, we first review clinical studies on sex differences in psychostimulant and opioid craving and relapse. Next, we review preclinical studies on sex differences in psychostimulant and opioid reinstatement of drug seeking after extinction of drug self-administration and incubation of drug craving (time-dependent increase in drug seeking during abstinence). We also discuss ovarian hormones’ role in relapse and craving in humans and animal models and speculate on brain mechanisms underlying their role in cocaine craving and relapse in rodent models. Finally, we discuss imaging studies on brain responses to cocaine cues and stress in men and women.The results of the clinical studies reviewed do not appear to support the notion that women are more vulnerable to psychostimulant and opioid craving and relapse. However, this conclusion is tentative because most of the studies reviewed were correlational, not sufficiently powered, and/or not a priori designed to detect sex differences. Additionally, fMRI studies suggest sex differences in brain responses to cocaine cues and stress. The results of the preclinical studies reviewed provide evidence for sex differences in stress-induced reinstatement and incubation of cocaine craving, but not cue- or cocaine priming-induced reinstatement of cocaine seeking. These sex differences are modulated in part by ovarian hormones. In contrast, the available data do not support the notion of sex differences in craving and relapse/reinstatement for methamphetamine or heroin in rodent models.


2007 ◽  
Vol 68 (5) ◽  
pp. 641-648 ◽  
Author(s):  
Damaris J. Rohsenow ◽  
Rosemarie A. Martin ◽  
Cheryl A. Eaton ◽  
Peter M. Monti

Author(s):  
Anna R. Childress ◽  
A. Thomas McLellan ◽  
Ronald Ehrman ◽  
Charles P. O'Brien

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