Biobehavioral Imaging and Molecular Neuropsychopharmacology Unit, National Institute on Drug Abuse Intramural Research Program, Baltimore, 21224, MD, USA.
Departament de Patologia i Terapèutica Experimental, Institut de Neurociències, Universitat de Barcelona, L'Hospitalet de Llobregat, 08907, Catalonia, Spain.
Mol Psychiatry. 2022 Oct;27(10):4144-4156. doi: 10.1038/s41380-022-01673-w. Epub 2022 Jun 29.
The off-label use of racemic ketamine and the FDA approval of (S)-ketamine are promising developments for the treatment of depression. Nevertheless, racemic ketamine and (S)-ketamine are controlled substances with known abuse potential and their use is associated with undesirable side effects. For these reasons, research efforts have focused on identifying alternatives. One candidate is (2R,6R)-hydroxynorketamine ((2R,6R)-HNK), a ketamine metabolite that in preclinical models lacks the dissociative and abuse properties of ketamine while retaining its antidepressant-like behavioral efficacy. (2R,6R)-HNK's mechanism of action however is unclear. The main goals of this study were to perform an in-depth pharmacological characterization of (2R,6R)-HNK at known ketamine targets, to use target deconvolution approaches to discover novel proteins that bind to (2R,6R)-HNK, and to characterize the biodistribution and behavioral effects of (2R,6R)-HNK across several procedures related to substance use disorder liability. We found that unlike (S)- or (R)-ketamine, (2R,6R)-HNK did not directly bind to any known or proposed ketamine targets. Extensive screening and target deconvolution experiments at thousands of human proteins did not identify any other direct (2R,6R)-HNK-protein interactions. Biodistribution studies using radiolabeled (2R,6R)-HNK revealed non-selective brain regional enrichment, and no specific binding in any organ other than the liver. (2R,6R)-HNK was inactive in conditioned place preference, open-field locomotor activity, and intravenous self-administration procedures. Despite these negative findings, (2R,6R)-HNK produced a reduction in immobility time in the forced swim test and a small but significant increase in metabolic activity across a network of brain regions, and this metabolic signature differed from the brain metabolic profile induced by ketamine enantiomers. In sum, our results indicate that (2R,6R)-HNK does not share pharmacological or behavioral profile similarities with ketamine or its enantiomers. However, it could still be possible that both ketamine and (2R,6R)-HNK exert antidepressant-like efficacy through a common and previously unidentified mechanism. Given its pharmacological profile, we predict that (2R,6R)-HNK will exhibit a favorable safety profile in clinical trials, and we must wait for clinical studies to determine its antidepressant efficacy.
消旋氯胺酮的非适应证使用和(S)-氯胺酮获得 FDA 批准,为抑郁症的治疗带来了新的希望。然而,消旋氯胺酮和(S)-氯胺酮是具有已知滥用潜力的受控物质,其使用与不良副作用有关。出于这些原因,研究工作集中在寻找替代品上。一个候选药物是(2R,6R)-羟基去甲氯胺酮((2R,6R)-HNK),它是氯胺酮的一种代谢物,在临床前模型中缺乏氯胺酮的分离和滥用特性,同时保留其抗抑郁样行为功效。然而,(2R,6R)-HNK 的作用机制尚不清楚。本研究的主要目标是在已知的氯胺酮靶点上对(2R,6R)-HNK 进行深入的药理学特征描述,使用靶点分解方法发现与(2R,6R)-HNK 结合的新蛋白,并对(2R,6R)-HNK 在与物质使用障碍易感性相关的几种程序中的生物分布和行为效应进行特征描述。我们发现,与(S)-或(R)-氯胺酮不同,(2R,6R)-HNK 不会直接与任何已知或提议的氯胺酮靶点结合。在数千个人类蛋白上进行广泛的筛选和靶点分解实验,没有发现任何其他直接的(2R,6R)-HNK-蛋白相互作用。使用放射性标记的(2R,6R)-HNK 的生物分布研究显示,非选择性脑区富集,除肝脏外,其他器官均无特异性结合。(2R,6R)-HNK 在条件性位置偏爱、旷场运动活性和静脉内自我给药程序中均无活性。尽管存在这些阴性结果,但(2R,6R)-HNK 可减少强迫游泳试验中的不动时间,并可在大脑区域网络中产生微小但显著的代谢活性增加,而这种代谢特征与氯胺酮对映体诱导的大脑代谢谱不同。总之,我们的结果表明,(2R,6R)-HNK 与氯胺酮或其对映体在药理学或行为特征上没有相似之处。然而,(2R,6R)-HNK 仍有可能通过一个共同的、以前未知的机制发挥抗抑郁样作用。鉴于其药理学特征,我们预测(2R,6R)-HNK 在临床试验中具有良好的安全性,我们必须等待临床研究来确定其抗抑郁疗效。