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Clinical neuropharmacology of cocaine reinforcement: A narrative review of human laboratory self-administration studies.可卡因强化的临床神经药理学:人类实验室自我给药研究的叙述性综述。
J Exp Anal Behav. 2022 May;117(3):420-441. doi: 10.1002/jeab.744. Epub 2022 Mar 1.
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Distinct contributions of dopamine in the dorsolateral striatum and nucleus accumbens shell to the reinforcing properties of cocaine.多巴胺在背外侧纹状体和伏隔核壳中的不同贡献可卡因强化性质。
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Effects of chronic methylphenidate on cocaine self-administration under a progressive-ratio schedule of reinforcement in rhesus monkeys.美金刚对恒河猴可卡因递增比例自我给药的影响。
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Human laboratory models of reward in substance use disorder.物质使用障碍中的人类奖励实验室模型。
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Cocaine self-administration behavior is associated with subcortical and cortical morphometry measures in individuals with cocaine use disorder.可卡因自我给药行为与可卡因使用障碍个体的皮质下和皮质形态计量学测量指标相关。
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N-Acetylcysteine: A Review of Clinical Usefulness (an Old Drug with New Tricks).N-乙酰半胱氨酸:临床应用综述(一种有新用途的老药)
J Nutr Metab. 2021 Jun 9;2021:9949453. doi: 10.1155/2021/9949453. eCollection 2021.
2
Topiramate-phentermine combinations reduce cocaine self-administration in humans.托吡酯-苯丁胺联合使用可减少人类可卡因的自我给药。
Drug Alcohol Depend. 2021 Jan 1;218:108413. doi: 10.1016/j.drugalcdep.2020.108413. Epub 2020 Nov 23.
3
Increase in Drug Overdose Deaths Involving Cocaine: United States, 2009-2018.可卡因滥用致死人数增加:美国,2009-2018 年。
NCHS Data Brief. 2020 Oct(384):1-8.
4
Cocaine use and overdose mortality in the United States: Evidence from two national data sources, 2002-2018.美国可卡因使用和过量用药死亡情况:来自两个国家数据源的证据,2002-2018 年。
Drug Alcohol Depend. 2020 Sep 1;214:108148. doi: 10.1016/j.drugalcdep.2020.108148. Epub 2020 Jul 15.
5
N-acetylcysteine reduces cocaine-seeking behavior and anterior cingulate glutamate/glutamine levels among cocaine-dependent individuals.N-乙酰半胱氨酸可减少可卡因依赖者的觅药行为和扣带前回谷氨酸/谷氨酰胺水平。
Addict Biol. 2021 Mar;26(2):e12900. doi: 10.1111/adb.12900. Epub 2020 Mar 24.
6
Rivastigmine does not alter cocaine-induced subjective effects or self-administration.利斯的明不改变可卡因引起的主观效应或自身给药。
Pharmacol Biochem Behav. 2019 Oct;185:172758. doi: 10.1016/j.pbb.2019.172758. Epub 2019 Aug 17.
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Pharmacological validation of a translational model of cocaine use disorder: Effects of d-amphetamine maintenance on choice between intravenous cocaine and a nondrug alternative in humans and rhesus monkeys.可卡因使用障碍转化模型的药理学验证:d-苯丙胺维持对人类和恒河猴静脉内可卡因与非药物替代物之间选择的影响。
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Influence of phendimetrazine maintenance on the reinforcing, subjective, performance, and physiological effects of intranasal cocaine.苯丙胺维持治疗对鼻内可卡因的强化、主观、表现和生理效应的影响。
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可卡因强化的临床神经药理学:人类实验室自我给药研究的叙述性综述。

Clinical neuropharmacology of cocaine reinforcement: A narrative review of human laboratory self-administration studies.

机构信息

Department of Behavioral Science, University of Kentucky College of Medicine.

Department of Psychiatry, University of Kentucky College of Medicine.

出版信息

J Exp Anal Behav. 2022 May;117(3):420-441. doi: 10.1002/jeab.744. Epub 2022 Mar 1.

DOI:10.1002/jeab.744
PMID:35229294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9090960/
Abstract

Cocaine use is an unrelenting public health concern. To inform intervention and prevention efforts, it is crucial to develop an understanding of the clinical neuropharmacology of the reinforcing effects of cocaine. The purpose of this review is to evaluate and synthesize human laboratory studies that assess pharmacological manipulations of cocaine self-administration. Forty-one peer-reviewed, human cocaine self-administration studies in which participants received a pretreatment drug were assessed. The pharmacological action and treatment regimen for all drugs reviewed were considered. Drugs that increase extracellular dopamine tend to have the most consistent effects on cocaine self-administration. The ability of nondopaminergic drugs to impact cocaine reinforcement might be related to their downstream effects on dopamine, though it is difficult to draw conclusions because pharmacologically selective compounds are not widely available for human testing. The ability of acute versus chronic drug treatment to differentially affect human cocaine self-administration was not determined because buprenorphine was the only pretreatment drug that was assessed under both acute and chronic dosing regimens. Future research directly comparing acute and chronic drug treatment and/or comparing drugs with different mechanisms of action, is needed to make more conclusive determinations about the clinical neuropharmacology of cocaine reinforcement.

摘要

可卡因的使用是一个持续存在的公共卫生问题。为了为干预和预防措施提供信息,了解可卡因的强化作用的临床神经药理学至关重要。本综述的目的是评估和综合评估评估可卡因自我给药的药理学操作的人体实验室研究。评估了 41 项经过同行评审的、参与者接受预处理药物的人类可卡因自我给药研究。考虑了所有审查药物的药理作用和治疗方案。增加细胞外多巴胺的药物往往对可卡因自我给药有最一致的影响。非多巴胺能药物对可卡因强化的影响能力可能与其对多巴胺的下游影响有关,但由于用于人体测试的药理学选择性化合物并不广泛,因此很难得出结论。由于丁丙诺啡是唯一一种在急性和慢性给药方案下都进行评估的预处理药物,因此无法确定急性与慢性药物治疗的能力差异是否会影响人类可卡因自我给药。需要进行直接比较急性和慢性药物治疗的未来研究,和/或比较具有不同作用机制的药物,以对可卡因强化的临床神经药理学做出更具结论性的确定。