Environmental determinants of ketamine's prohedonic and antianhedonic efficacy: Persistence of enhanced reward responsiveness is modulated by chronic stress.

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Amaya R Jenkins, Daniela B Radl, Thomas J Kornecook, Diego A Pizzagalli, Jack Bergman, Derek L Buhl, Patricio O'Donnell, Brian D Kangas
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引用次数: 0

Abstract

Ketamine, a dissociative anesthetic with well documented abuse liability, can also provide rapid-onset and persistent antidepressant effects and is currently used for the management of treatment-resistant depression. Although the precise neurobiological mechanisms underlying its antidepressant actions are not fully determined, a critical feature of ketamine's clinical efficacy may be its antianhedonic action. Anhedonia is an endophenotype of depression defined by decreased responsivity to previously rewarding stimuli and is generally not ameliorated by conventional antidepressants, emphasizing the need to examine underlying behavioral mechanisms of action. In this study, the probabilistic reward task, a reverse-translated assay originally designed to objectively quantify anhedonic phenotypes in human subjects, was used in rats to examine ketamine's effects on reward responsiveness under conditions without programmed stressors (3.2-32.0 mg/kg) or during ongoing chronic exposure to ecologically relevant stress (10.0 mg/kg). Results showed that under conditions without programmed stress, ketamine produced significant prohedonic effects in the probabilistic reward task, defined by increases in reward responsiveness that dissipated within 24 hours. In rats exposed to ongoing chronic stress, ketamine produced significant antianhedonic effects, defined by the rescue of blunted reward responsiveness, that persisted for nearly 1 week. Taken together, the prolonged antianhedonic effects of ketamine in rats experiencing chronic stress, compared with the shorter-lived prohedonic effects in subjects without exposure to programmed stressors, are striking and highlight the role of environmental determinants in the effects of ketamine on behavioral processes. Moreover, the translational nature of this experimental design may offer the opportunity to accelerate development of novel antianhedonic therapeutics. SIGNIFICANCE STATEMENT: Although ketamine is used for the management of treatment-resistant depression, its precise behavioral mechanisms of action are not fully delineated. Emerging evidence suggests the attenuation of anhedonia plays a key role in its rapid-acting therapeutic efficacy. To evaluate this possibility, the effects of ketamine were studied using a reverse-translated assay of reward responsiveness in rats and documented to be short-lived (prohedonic) under nonstressful conditions and persistent (antianhedonic) under stressful conditions, informing ketamine effects in healthy versus depressed individuals.

氯胺酮的快感和反快感效能的环境决定因素:持续增强的奖励反应是由慢性应激调节的。
氯胺酮是一种解离性麻醉剂,有充分证据表明它有滥用的危险,也可以提供快速发作和持续的抗抑郁作用,目前用于治疗难治性抑郁症。虽然其抗抑郁作用的确切神经生物学机制尚未完全确定,但氯胺酮临床疗效的一个关键特征可能是其抗快感缺乏作用。快感缺乏症是抑郁症的一种内表型,其特征是对先前有益刺激的反应性降低,通常不能通过传统的抗抑郁药物得到改善,这强调了研究潜在行为机制的必要性。在这项研究中,概率奖励任务(一种最初设计用于客观量化人类受试者快感缺乏表型的反向翻译试验)被用于大鼠,以检查氯胺酮在没有程序性应激源(3.2-32.0 mg/kg)或持续慢性暴露于生态相关应激(10.0 mg/kg)的条件下对奖励反应的影响。结果表明,在没有程序性应激的条件下,氯胺酮在概率奖励任务中产生了显著的前快感效应,即奖励反应的增加在24小时内消失。在暴露于持续慢性应激的大鼠中,氯胺酮产生了显著的抗快感缺乏作用,通过对迟钝的奖励反应的拯救来定义,这种作用持续了近一周。综上所述,氯胺酮对经历慢性应激的大鼠的长期抗快感缺乏作用,与未暴露于程序性应激源的受试者的短期快感缺乏作用相比,是惊人的,并突出了环境决定因素在氯胺酮对行为过程的影响中的作用。此外,这种实验设计的翻译性质可能为加速新型抗快感缺乏疗法的发展提供机会。意义声明:虽然氯胺酮被用于治疗难治性抑郁症,但其确切的行为机制尚未完全描述。越来越多的证据表明,快感缺乏症的减轻在其速效治疗效果中起着关键作用。为了评估这种可能性,在大鼠中使用反向翻译的奖励反应试验研究了氯胺酮的作用,并记录了在无压力条件下的短暂性(快感缺乏性)和在压力条件下的持续性(反快感缺乏性),说明氯胺酮在健康个体和抑郁个体中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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