Seeking under threat of adversity: assessing control over reward pursuit in rats.

IF 3.5 3区 医学 Q2 NEUROSCIENCES Psychopharmacology Pub Date : 2024-12-10 DOI:10.1007/s00213-024-06729-z
Sofie van Koppen, A Maryse Minnaard, Johanna A S Smeets, Iulia Buzatouiu, Geert M J Ramakers, Roger A H Adan, Louk J M J Vanderschuren, Heidi M B Lesscher
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Abstract

Rationale: Substance use disorder (SUD) is a chronic relapsing brain disorder that is characterised by loss of control over substance use. A variety of rodent models employing punishment setups have been developed to assess loss of control over substance use, i.e. persistent substance use despite negative consequences, to facilitate the translation of findings from animal studies to the human situation.

Objectives: Since the negative consequences of addictive behaviour are typically unpredictable, we here present the Seeking under Threat of Adversity (STA) task in rats, that incorporates cued, probabilistic and response-contingent punishment of reward seeking.

Methods: Male rats were trained to lever press for sucrose, alcohol or cocaine and were subsequently tested in the STA task. In this task, a tone cue is presented during reward seeking which functions as a warning signal, since responding during tone presentation results in a probabilistic foot shock punishment. We first determined the optimal shock intensity to induce a moderate suppression of seeking. Next, we assessed the stability of punished reward seeking over repeated tests. Finally, we compared the development of loss of control over substance seeking for sucrose, alcohol and cocaine. (Loss of) control over substance seeking would be evident as the (in)ability to refrain from lever pressing to obtain a reward, despite the threat of a negative outcome.

Results: Parametric experiments revealed suppression of responding for both sucrose and alcohol in the STA task at shock intensities between 0.25 and 0.35 mA. The suppression of responding was stable with repeated testing. Furthermore, less control over alcohol and cocaine seeking, when compared to sucrose seeking, was observed in male rats using the STA task.

Conclusions: The STA task is a novel behavioural task that includes two important aspects of human substance use despite negative consequences, i.e. response contingency and unpredictability of adversity. Combined with other behavioural tasks and neural manipulations, the STA task can further our understanding of the psychopathology of substance use disorders.

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逆境威胁下的追寻:评估大鼠对奖励追寻的控制。
理由:物质使用障碍(SUD)是一种慢性复发性脑障碍,其特征是对物质使用失去控制。已经开发了采用惩罚设置的各种啮齿动物模型,以评估对物质使用的失去控制,即不顾负面后果持续使用物质,以促进将动物研究结果转化为人类情况。目的:由于成瘾行为的负面后果通常是不可预测的,我们在这里提出了在逆境威胁下寻求(STA)的大鼠任务,该任务结合了奖励寻求的线索、概率和反应偶然惩罚。方法:将雄性大鼠训练成杠杆按压蔗糖、酒精或可卡因,然后进行STA任务测试。在这个任务中,在寻求奖励的过程中会出现一个音调提示,作为一个警告信号,因为在音调呈现过程中做出反应会导致概率性的足部电击惩罚。我们首先确定了最佳的冲击强度,以诱导适度的寻找抑制。接下来,我们评估了在重复测试中惩罚奖励寻求的稳定性。最后,我们比较了对蔗糖、酒精和可卡因的物质寻求失去控制的发展。(失去)对物质寻求的控制将表现为,尽管有负面结果的威胁,但(缺乏)抑制按杠杆获得奖励的能力。结果:参数实验显示,在0.25 ~ 0.35 mA的冲击强度下,STA任务中蔗糖和酒精的反应均受到抑制。经反复试验,反应抑制稳定。此外,与蔗糖寻求相比,在STA任务中,在雄性大鼠中观察到对酒精和可卡因寻求的控制较少。STA任务是一种新的行为任务,包括人类物质使用的两个重要方面,即逆境的反应偶然性和不可预测性。STA任务与其他行为任务和神经操作相结合,可以进一步加深我们对物质使用障碍的精神病理学的理解。
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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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