Department of Psychiatry & Behavioral Sciences, University of Washington School of Medicine, Seattle, Washington, USA.
Mental Illness Research, Education and Clinical Center, Puget Sound VA Health Care System, Seattle, Washington, USA.
Addict Biol. 2023 Dec;28(12):e13344. doi: 10.1111/adb.13344.
Opioid use disorder has become an epidemic in the United States, fuelled by the widespread availability of fentanyl, which produces rapid and intense euphoria followed by severe withdrawal and emotional distress. We developed a new preclinical model of fentanyl seeking in outbred male and female rats using volitional oral self-administration (SA) that can be readily applied in labs without intravascular access. Using a traditional two-lever operant procedure, rats learned to take oral fentanyl vigorously, escalated intake across sessions, and readily reinstated responding to conditioned cues after extinction. Oral SA also revealed individual and sex differences that are essential to studying substance use risk propensity. During a behavioural economics task, rats displayed inelastic demand curves and maintained stable intake across a wide range of fentanyl concentrations. Oral SA was also neatly patterned, with distinct 'loading' and 'maintenance' phases of responding within each session. Using our software DeepSqueak, we analysed ultrasonic vocalizations (USVs), which are innate expressions of current emotional state in rats. Rats produced 50 kHz USVs during loading then shifted quickly to 22 kHz calls despite ongoing maintenance of oral fentanyl taking, reflecting a transition to negative reinforcement. Using fibre photometry, we found that the lateral habenula differentially processed drug cues and drug consumption depending on affective state, with potentiated modulation by drug cues and consumption during the negative affective maintenance phase. Together, these results indicate a rapid progression from positive to negative reinforcement occurs even within an active drug taking session, revealing a within-session opponent process.
阿片类药物使用障碍已成为美国的一种流行病,芬太尼的广泛可获得性是其主要原因,芬太尼会迅速产生强烈的欣快感,随后会出现严重的戒断和情绪困扰。我们开发了一种新的用于检测芬太尼觅药行为的临床前模型,该模型使用自愿口服自我给药(SA),在不需要血管内通路的情况下,可在实验室中轻松应用。通过传统的双杆操作性条件反射程序,大鼠学会了积极地口服芬太尼,在各次试验中增加了摄入量,并在消退后很容易重新对条件线索做出反应。口服 SA 还揭示了个体和性别差异,这些差异对于研究物质使用风险倾向至关重要。在行为经济学任务中,大鼠显示出无弹性的需求曲线,并在广泛的芬太尼浓度范围内保持稳定的摄入量。口服 SA 也被整齐地设计,在每次试验中都有明显的“加载”和“维持”阶段的反应。使用我们的 DeepSqueak 软件,我们分析了超声波发声(USVs),这是大鼠当前情绪状态的固有表达。大鼠在加载过程中产生 50 kHz 的 USVs,然后迅速转换为 22 kHz 的叫声,尽管仍在继续维持口服芬太尼的摄入,这反映了向负强化的转变。使用光纤光度法,我们发现外侧缰核根据情绪状态对药物线索和药物消耗进行不同的处理,在负性情绪维持阶段,药物线索和消耗会增强调节作用。这些结果表明,即使在主动药物摄入过程中,也会迅速从正强化转变为负强化,这揭示了一种在单次试验内的对抗过程。