Decreased incubation of fentanyl seeking in the absence of proximal drug-paired stimuli.

IF 2.4 3区 医学 Q3 PHARMACOLOGY & PHARMACY Experimental and clinical psychopharmacology Pub Date : 2025-01-02 DOI:10.1037/pha0000763
Justin R Yates, Maria R Broderick
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Abstract

Treating substance use disorders is difficult as individuals often resume substance use during abstinence. One potential factor contributing to the recurrence of substance use is incubation of drug craving. Specifically, individuals report higher levels of craving when presented with drug-paired stimuli across abstinence, although this effect is largely absent in opioid-dependent individuals. In preclinical studies, rodents show increased responding on a previously reinforced manipulandum when presented with drug cues, including for opioids. When proximal cues are not presented, self-reported craving tends to decrease across abstinence; however, incubation of drug seeking in the absence of proximal stimuli is rarely tested in animals. As such, we trained male and female Sprague Dawley rats to self-administer the synthetic opioid fentanyl (2.5 μg/kg/infusion) during ten 60-min sessions. Rats were then given three extinction sessions on Days 1, 21, and 30 of withdrawal. Unlike other studies measuring incubation of craving, we did not present drug-paired stimuli (e.g., stimulus lights) during these extinction sessions. Incubation of fentanyl seeking was not observed in the present experiment; instead, responses on the previously drug-paired lever tended to decrease across the three extinction sessions. Based on the results of this experiment, we provide a discussion of some potential interpretational issues associated with the incubation of craving paradigm, including the difficulty in dissociating drug craving from operant sensation seeking (i.e., rodents will respond on a manipulandum to earn access to audiovisual cues that are presented alone). (PsycInfo Database Record (c) 2025 APA, all rights reserved).

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在没有近端药物配对刺激的情况下,芬太尼寻找的潜伏期减少。
治疗物质使用障碍是困难的,因为个人经常在戒断期间恢复物质使用。导致药物使用复发的一个潜在因素是药物渴望的潜伏期。具体来说,当在戒断过程中出现药物配对刺激时,个体报告的渴望水平更高,尽管这种影响在阿片类药物依赖个体中基本不存在。在临床前研究中,啮齿类动物在药物提示(包括阿片类药物)时,对先前强化的操纵性反应增加。当不提供近端提示时,自我报告的渴望倾向于在禁欲期间减少;然而,在没有近端刺激的情况下,寻找药物的潜伏期很少在动物身上进行试验。因此,我们训练雄性和雌性Sprague Dawley大鼠在10个60分钟的疗程中自我施用合成阿片类药物芬太尼(2.5 μg/kg/输注)。然后在戒断的第1天、第21天和第30天给予大鼠3次消失疗程。与其他测量渴望潜伏期的研究不同,我们在这些消退过程中没有提供药物配对刺激(例如刺激光)。本实验未观察到芬太尼寻找的潜伏期;相反,在先前的药物配对杠杆上的反应在三个消失过程中趋于减少。基于本实验的结果,我们讨论了与渴望范式孵化相关的一些潜在解释问题,包括将药物渴望与操作性感觉寻求分离的困难(即,啮齿动物将对操纵物做出反应,以获得单独呈现的视听线索)。(PsycInfo Database Record (c) 2025 APA,版权所有)。
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来源期刊
CiteScore
4.20
自引率
8.70%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Experimental and Clinical Psychopharmacology publishes advances in translational and interdisciplinary research on psychopharmacology, broadly defined, and/or substance abuse.
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