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(2R,6R)-羟基去甲氯胺酮可预防小鼠阿片类药物戒断相关的负面影响和应激诱导的复吸。

(2R,6R)-hydroxynorketamine prevents opioid abstinence-related negative affect and stress-induced reinstatement in mice.

作者信息

Michael Andria, Onisiforou Anna, Georgiou Polymnia, Koumas Morfeas, Powels Chris, Mammadov Elmar, Georgiou Andrea N, Zanos Panos

机构信息

Department of Psychology, University of Cyprus, Nicosia, Cyprus.

Center for Applied Neuroscience (CAN), University of Cyprus, Nicosia, Cyprus.

出版信息

Br J Pharmacol. 2025 Mar 28. doi: 10.1111/bph.70018.

Abstract

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.

摘要

背景与目的

阿片类物质使用障碍(OUD)是一个紧迫的公共卫生问题,其特征是在禁欲期间频繁复发,由负面情绪状态持续存在。经典抗抑郁药或目前规定的阿片类药物疗法在逆转负面影响或预防复发方面疗效有限。

实验方法

我们使用小鼠模型,研究了氯胺酮的代谢物(2R,6R)-羟基去甲氯胺酮(HNK)对逆转应激易感小鼠对亚有效剂量吗啡的条件反射、预防条件性位置厌恶以及减轻阿片类药物依赖小鼠的急性躯体戒断症状的影响。此外,我们评估了其对长期阿片类药物戒断期间快感缺失、焦虑样行为和认知障碍的影响,同时进行的机制研究检测了皮质脑电图振荡和突触可塑性标记物。

主要结果

(2R,6R)-HNK逆转了应激易感小鼠对亚有效剂量吗啡的条件反射,并预防了阿片类药物依赖小鼠的条件性位置厌恶和急性躯体戒断症状。此外,(2R,6R)-HNK可能通过恢复受损的皮质高频脑电图振荡,通过依赖GluN2A-NMDA受体的机制,逆转了长期阿片类药物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促进了阿片类药物条件反射的消退,预防了应激诱导的阿片类药物寻求行为的恢复,并降低了先前接触过阿片类药物的小鼠增加吗啡自我给药的倾向。

结论与启示

这些发现强调了目前正处于II期临床试验的(2R,6R)-HNK在应对与应激相关的阿片类反应方面的治疗潜力。由于我们目前面临阿片类药物危机,通过药物重新利用来减少开发用于治疗OUDs的新药物所需的时间和成本至关重要。

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