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Aripiprazole maintenance increases smoked cocaine self-administration in humans.阿立哌唑维持治疗增加人类吸食可卡因的自我给药。
Psychopharmacology (Berl). 2011 Aug;216(3):379-87. doi: 10.1007/s00213-011-2231-6. Epub 2011 Mar 5.
2
The effects of oral micronized progesterone on smoked cocaine self-administration in women.口服微粒化黄体酮对女性吸烟可卡因自我给药的影响。
Horm Behav. 2011 Feb;59(2):227-35. doi: 10.1016/j.yhbeh.2010.12.009. Epub 2010 Dec 28.
3
Using a novel alternative to drug choice in a human laboratory model of a cocaine binge: a game of chance.在人类可卡因狂欢实验室模型中使用一种新颖的药物选择替代方法:机会游戏。
Drug Alcohol Depend. 2010 Jul 1;110(1-2):144-50. doi: 10.1016/j.drugalcdep.2010.02.015. Epub 2010 Mar 25.
4
Effects of acute psychosocial stress on cigarette craving and smoking.急性心理社会应激对吸烟渴求感和吸烟的影响。
Nicotine Tob Res. 2010 Apr;12(4):449-53. doi: 10.1093/ntr/ntp214. Epub 2010 Jan 25.
5
Polymorphisms in dopamine transporter (SLC6A3) are associated with stimulant effects of D-amphetamine: an exploratory pharmacogenetic study using healthy volunteers.多巴胺转运体(SLC6A3)多态性与 D-苯丙胺的兴奋剂效应有关:一项使用健康志愿者的探索性药物遗传学研究。
Behav Genet. 2010 Mar;40(2):255-61. doi: 10.1007/s10519-009-9331-7. Epub 2010 Jan 21.
6
Modafinil does not serve as a reinforcer in cocaine abusers.莫达非尼对可卡因滥用者不起强化作用。
Drug Alcohol Depend. 2010 Jan 15;106(2-3):233-6. doi: 10.1016/j.drugalcdep.2009.09.002. Epub 2009 Sep 23.
7
Last observation carried forward versus mixed models in the analysis of psychiatric clinical trials.精神病学临床试验分析中的末次观察结转法与混合模型
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Substitute addiction: a concern for researchers and practitioners.替代成瘾:研究人员和从业者关注的问题。
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Drug Alcohol Depend. 2008 Jul 1;96(1-2):1-15. doi: 10.1016/j.drugalcdep.2008.03.001. Epub 2008 Apr 24.
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参与涉及吸食可卡因自我给药的实验室研究后的物质使用情况。

Substance use after participation in laboratory studies involving smoked cocaine self-administration.

机构信息

Substance Use Research Center, Columbia University, New York, NY 10032, United States.

出版信息

Drug Alcohol Depend. 2012 Jan 1;120(1-3):162-7. doi: 10.1016/j.drugalcdep.2011.07.015. Epub 2011 Aug 15.

DOI:10.1016/j.drugalcdep.2011.07.015
PMID:21840650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3228895/
Abstract

OBJECTIVE

Laboratory studies in which drugs of abuse are self- or experimenter-administered to non-treatment-seeking research volunteers provide valuable data about new pharmacotherapies for substance use disorders, as well as behavioral and performance data for understanding the neurobiology of drug abuse. This paper analyzed follow-up data from six smoked cocaine self-administration laboratory studies, in order to determine whether changes in substance use occurred 1 and 3 months after study participation compared to pre-study baseline.

METHODS

Ninety-eight healthy, non-treatment-seeking cocaine users were admitted to inpatient and combined inpatient/outpatient studies lasting from 12 to 105 days. The studies allowed participants to self-administer repeated doses of smoked cocaine (0, 6, 12, 25, and/or 50mg per dose) on multiple occasions. Participants returned for follow-up at 1 and 3 months, at which time self-reported consumption of cocaine, alcohol, marijuana, and nicotine was assessed.

RESULTS

Compared to baseline ($374.04/week, S.D. $350.09), cocaine use significantly decreased at 1 month ($165.13/week, S.D. $165.56) and 3 months ($118.59/week, S.D. $110.48) after study participation (p<0.001; results based on the 39 participants who completed all 3 time points). This decrease was not accompanied by a change in other drug use, e.g., a compensatory increase in alcohol, marijuana or nicotine use.

CONCLUSION

Study participation was not associated with increased post-study cocaine, alcohol, marijuana, or nicotine use. Thus, human laboratory models of cocaine self-administration, conducted in non-treatment-seeking research volunteers, are relatively safe, and study participation does not exacerbate ongoing drug use.

摘要

目的

在非治疗寻求者的研究志愿者中自我或实验者给予滥用药物的实验室研究为物质使用障碍的新药物治疗提供了有价值的数据,以及理解药物滥用神经生物学的行为和表现数据。本文分析了六项吸食可卡因自我给药实验室研究的随访数据,以确定与研究前基线相比,在研究参与后 1 个月和 3 个月是否发生了物质使用的变化。

方法

98 名健康、非治疗寻求的可卡因使用者被收入住院和联合住院/门诊研究,持续 12 至 105 天。这些研究允许参与者多次自我给予吸食可卡因(0、6、12、25 和/或 50mg 剂量)的重复剂量。参与者在 1 个月和 3 个月时返回进行随访,此时评估自我报告的可卡因、酒精、大麻和尼古丁的使用情况。

结果

与基线相比($374.04/周,S.D. $350.09),在研究参与后 1 个月($165.13/周,S.D. $165.56)和 3 个月($118.59/周,S.D. $110.48)可卡因使用显著减少(p<0.001;基于完成所有 3 个时间点的 39 名参与者的结果)。这种减少没有伴随着其他药物使用的变化,例如酒精、大麻或尼古丁使用的代偿性增加。

结论

研究参与与研究后可卡因、酒精、大麻或尼古丁使用的增加无关。因此,在非治疗寻求者的研究志愿者中进行的可卡因自我给药人类实验室模型相对安全,并且研究参与不会加剧正在进行的药物使用。