在强迫戒除芬太尼期间,在大鼠赌博任务中的风险选择增加。

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Kelly M Hrelja, Carol Kawkab, Dimitrios K Avramidis, Shrishti Ramaiah, Catharine A Winstanley
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引用次数: 0

摘要

理由:非法阿片类药物的使用可以说从未像现在这样具有如此大的风险;街头毒品的药效可能非常高,消费者往往并不知晓,而且每天都会在全球范围内造成多起死亡事故。此外,在基于实验室的赌博任务中,药物使用障碍(SUD)与不适应性风险决策增加有关。动物实验可以帮助确定这种决策缺陷是吸毒的原因还是后果。然而,大多数实验只评估了精神兴奋剂药物:评估雌雄 Long Evans 大鼠在自我注射芬太尼之前、期间和之后的决策策略差异:对雌雄 Long Evans 大鼠进行训练,让它们完成大鼠赌博任务(rGT)和/或自我注射芬太尼,该任务大致基于临床上使用的爱荷华赌博任务(IGT)。我们使用的是提示版的rGT,其中声光刺激是糖丸奖励的信号,因为在这种任务变体中,可卡因自我给药对决策的影响最大:结果:在接受了有提示的 rGT 训练后,雌性大鼠更容易自我给药芬太尼,这种效应在最佳决策者中最为明显。与之前使用可卡因自我给药的报告相反,在芬太尼自我给药训练中,雌雄大鼠的决策均不受影响。然而,男性在强迫戒断芬太尼的过程中,风险决策会增加:这些发现补充了人类受试者的研究结果,在人类受试者中,对不确定结果的偏好在复吸前会增加。这些数据突显了鸦片制剂与精神兴奋剂相比所特有的戒断诱导的认知变化,这种变化可能对成瘾的维持和复发起到至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Increased risky choice during forced abstinence from fentanyl on the cued rat gambling task.

Increased risky choice during forced abstinence from fentanyl on the cued rat gambling task.

Rationale: The use of illicit opioids has arguably never been more risky; street drug potency can be dangerously high, is often unknown to the consumer, and results in multiple daily fatalities worldwide. Furthermore, substance use disorder (SUD) is associated with increased maladaptive, risky decisions in laboratory-based gambling tasks. Animal studies can help determine whether this decision-making deficit is a cause or consequence of drug use. However, most experiments have only assessed psychostimulant drugs.

Objectives: To assess differences in decision-making strategies both before, during, and after self-administration of fentanyl in male and female Long Evans rats.

Methods: Male and female Long Evans rats were trained to perform the rat gambling task (rGT), loosely based on the Iowa Gambling Task (IGT) used clinically, and/or self-administer fentanyl. We used the cued version of the rGT, in which sound and light stimuli signal sugar pellet rewards, as cocaine self-administration has the greatest effects on decision making in this task variant.

Results: After training on the cued rGT, female rats self-administered fentanyl more readily, an effect that was most apparent in optimal decision-makers. Contrary to previous reports using cocaine self-administration, decision-making was unaffected during fentanyl self-administration training in either sex. However, risky decision-making increased throughout forced abstinence from fentanyl in males.

Conclusions: These findings complement those from human subjects, in whom preference for uncertain outcomes increased before relapse. These data highlight an abstinence-induced change in cognition that is unique to opiates as compared to psychostimulants, and which may critically contribute to the maintenance of addiction and relapse.

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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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