(2R,6R)-羟基炔诺酮胺可防止小鼠产生与阿片类药物戒断相关的负性情绪和应激诱导的恢复。

IF 6.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Andria Michael, Anna Onisiforou, Polymnia Georgiou, Morfeas Koumas, Chris Powels, Elmar Mammadov, Andrea N Georgiou, Panos Zanos
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引用次数: 0

摘要

背景和目的:阿片类药物使用障碍(OUD)是一个紧迫的公共卫生问题,其特征是在戒断期间频繁复发,并因负面情感状态而长期存在。经典抗抑郁药或目前处方的阿片类药物治疗在逆转负面影响或防止复发方面的疗效有限。实验方法:采用小鼠模型,研究氯胺酮代谢物(2R,6R)-羟诺氯胺酮(HNK)对应激易感小鼠逆转对亚有效剂量吗啡的条件反射、预防条件性场所厌恶和缓解阿片类药物依赖小鼠急性躯体戒断症状的作用。此外,我们评估了其对阿片类药物长期戒断期间快感缺乏、焦虑样行为和认知障碍的影响,而机制研究检查了皮质脑电图振荡和突触可塑性标志物。关键结果:(2R,6R)-HNK逆转应激易感小鼠对亚有效剂量吗啡的条件反射,并预防阿片依赖小鼠的条件反射性场所厌恶和急性躯体戒断症状。此外,(2R,6R)-HNK通过GluN2A-NMDA受体依赖机制,通过恢复受损的皮质高频脑电图振荡,逆转了阿片类药物长期戒断期间出现的快感缺失、焦虑样行为和认知障碍。值得注意的是,(2R,6R)-HNK促进了阿片类物质条件反射的消失,防止应激诱导的阿片类物质寻求行为的恢复,并降低了先前暴露于阿片类物质的小鼠增强吗啡自我消耗的倾向。结论和意义:这些发现强调了(2R,6R)-HNK在解决压力相关阿片类药物反应方面的治疗潜力,该药物目前处于II期临床试验中。由于我们目前面临的阿片类药物危机,通过药物再利用来减少开发用于治疗oud的新药物所需的时间和成本至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
(2R,6R)-hydroxynorketamine prevents opioid abstinence-related negative affect and stress-induced reinstatement in mice.

Background and purpose: Opioid use disorder (OUD) is a pressing public health concern marked by frequent relapse during periods of abstinence, perpetuated by negative affective states. Classical antidepressants or the currently prescribed opioid pharmacotherapies have limited efficacy to reverse the negative affect or prevent relapse.

Experimental approach: Using mouse models, we investigated the effects of ketamine's metabolite (2R,6R)-hydroxynorketamine (HNK) on reversing conditioning to sub-effective doses of morphine in stress-susceptible mice, preventing conditioned-place aversion and alleviating acute somatic abstinence symptoms in opioid-dependent mice. Additionally, we evaluated its effects on anhedonia, anxiety-like behaviours and cognitive impairment during protracted opioid abstinence, while mechanistic studies examined cortical EEG oscillations and synaptic plasticity markers.

Key results: (2R,6R)-HNK reversed conditioning to sub-effective doses of morphine in stress-susceptible mice and prevented conditioned-place aversion and acute somatic abstinence symptoms in opioid-dependent mice. In addition, (2R,6R)-HNK reversed anhedonia, anxiety-like behaviours and cognitive impairment emerging during protracted opioid abstinence plausibly via a restoration of impaired cortical high-frequency EEG oscillations, through a GluN2A-NMDA receptor-dependent mechanism. Notably, (2R,6R)-HNK facilitated the extinction of opioid conditioning, prevented stress-induced reinstatement of opioid-seeking behaviours and reduced the propensity for enhanced morphine self-consumption in mice previously exposed to opioids.

Conclusions and implications: These findings emphasize the therapeutic potential of (2R,6R)-HNK, which is currently in Phase II clinical trials, in addressing stress-related opioid responses. Reducing the time and cost required for development of new medications for the treatment of OUDs via drug repurposing is critical due to the opioid crisis we currently face.

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来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
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