Renewal of cocaine seeking using social and nonsocial contextual stimuli.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2025-05-01 Epub Date: 2023-07-01 DOI:10.1007/s00213-023-06414-7
Bree A Humburg, Michael T Bardo
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引用次数: 0

Abstract

Rationale: Various nonsocial cues have been used as stimuli to examine the contextual control of drug seeking behavior, but little is known about the role of social stimuli.

Objectives: This study determined if renewal of cocaine seeking is differentially controlled using a context consisting of either a social peer and/or house light illumination.

Methods: In Experiment 1, male and female rats trained to self-administer cocaine in the presence of a same-sex social peer and house light illumination (context A). Following self-administration, rats were randomly assigned to either an AAA (control) or ABA (renewal) group for extinction. For AAA rats, extinction consisted of the same context A as self-administration; for ABA rats, extinction occurred without the peer or house light (context B). Following extinction, renewal of cocaine seeking occurred by testing the peer alone, house light alone, and the peer + house light combination. Experiment 2 was conducted to ensure that the house light alone was sufficiently salient to produce renewal.

Results: Both experiments showed that rats acquired cocaine self-administration and extinguished lever pressing. In Experiment 1, the ABA group renewed cocaine seeking to the peer and peer + house light, but not to the house light alone. In Experiment 2, ABA rats renewed cocaine seeking to the house light alone, indicating it was sufficiently salient to produce renewal. The AAA group did not show renewal in either experiment.

Conclusion: Social peers serve as powerful stimuli that can overshadow nonsocial visual stimuli in the renewal of cocaine seeking.

利用社会和非社会情境刺激重新寻求可卡因。
理论依据:各种非社交线索被用作刺激物来研究毒品寻求行为的情境控制,但人们对社交刺激物的作用知之甚少:本研究确定可卡因寻求行为的恢复是否会受到由社交同伴和/或室内灯光照明组成的情境的不同控制:在实验 1 中,雄性和雌性大鼠在同性社会同伴和室内灯光照明(情境 A)下接受可卡因自我给药训练。自我给药后,大鼠被随机分配到AAA组(对照组)或ABA组(更新组)进行消减。对于 AAA 组大鼠,灭效包括与自我给药相同的情境 A;对于 ABA 组大鼠,灭效则不包括同伴或室内灯光(情境 B)。灭绝后,通过单独测试同伴、单独测试室内灯光以及同伴+室内灯光组合,重新开始寻找可卡因。进行实验 2 的目的是确保单独的室内灯光有足够的显著性来产生可卡因寻求的恢复:结果:两项实验均表明,大鼠获得了可卡因自我给药并熄灭了杠杆按压。在实验 1 中,ABA 组大鼠对同伴和同伴 + 屋内灯光恢复了可卡因寻求,但对单独的屋内灯光没有恢复。在实验 2 中,ABA 组大鼠对单独的室内灯光重新产生了可卡因寻求,这表明室内灯光的显著性足以产生可卡因寻求的更新。而 AAA 组在这两个实验中都没有表现出可卡因寻求的恢复:结论:社交同伴是一种强有力的刺激,在可卡因寻求的恢复过程中可以盖过非社交的视觉刺激。
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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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