(S)-Ketamine but Not (R)-Ketamine Shows Acute Effects on Depression-Like Behavior and Sleep-Wake Architecture in Rats.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY
Szabolcs Koncz, Noémi Papp, Dóra Pothorszki, György Bagdy
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引用次数: 1

Abstract

Background: Racemic ketamine consists of two enantiomers, namely (R)-ketamine and (S)-ketamine, with distinguishable pharmacological properties. Both enantiomers have been reported to show rapid antidepressant effects in rodents. Currently, the (S)-enantiomer has been approved for the treatment of major depression, whereas (R)-ketamine failed to show antidepressant effect in recent clinical studies. Major depressive disorder is frequently characterized by disinhibition of rapid eye movement (REM) sleep and disruption of non-REM (NREM) sleep. Racemic ketamine and most conventional antidepressants affect these parameters. However, it remains largely unknown which enantiomer is responsible for these effects.

Methods: Here, we compared acute effects of the two ketamine enantiomers (15 mg/kg i.p.) on different sleep-wake stages in freely moving, EEG-equipped rats. We also evaluated the antidepressant-like activity of the enantiomers in a chronic restraint stress model of depression.

Results: (S)-ketamine but not (R)-ketamine increased REM sleep latency and decreased REM sleep time at 2 and 3 hours, and increased electroencephalogram delta power during NREM sleep. In addition, only (S)-ketamine increased wakefulness and decreased NREM sleep in the first 2 hours. In the forced swimming test, only (S)-ketamine decreased the immobility time of chronically stressed rats.

Conclusion: Effects of the two ketamine enantiomers on rat sleep-wake architecture and behavior are markedly different when administered in the same dose. (S)-ketamine remarkably affects the sleep-wake cycle and very likely sleep-related neuroplasticity, which may be relevant for its antidepressant efficacy. Our results regarding (R)-ketamine's lack of effect on vigilance and behavior are in line with recent clinical studies.

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(S) -氯胺酮而非(R)-氯胺酮对大鼠抑郁样行为和睡眠-觉醒结构具有急性影响。
背景:外消旋氯胺酮由两种对映体组成,即(R)-氯胺酮和(S)-氯胺酮,具有不同的药理学性质。据报道,这两种对映体在啮齿类动物中都显示出快速的抗抑郁作用。目前,(S)-对映异构体已被批准用于治疗重度抑郁症,而(R)-氯胺酮在最近的临床研究中未能显示出抗抑郁作用。重性抑郁症的特征通常是快速眼动(REM)睡眠的去抑制和非快速眼动(NREM)睡眠的中断。外消旋氯胺酮和大多数常规抗抑郁药会影响这些参数。然而,在很大程度上还不知道是哪种对映异构体造成了这些影响。方法:在这里,我们比较了两种氯胺酮对映体(15mg/kg i.p.)对自由移动、脑电图设备的大鼠不同睡眠-觉醒阶段的急性影响。我们还在抑郁症的慢性约束应激模型中评估了对映体的抗抑郁样活性。结果:(S)-氯胺酮而非(R)-氯胺酮在2小时和3小时增加了REM睡眠潜伏期,减少了REM睡眠时间,并增加了NREM睡眠期间的脑电图δ功率。此外,只有(S)-氯胺酮在最初的2小时内增加了清醒度并降低了NREM睡眠。在强迫游泳试验中,只有(S)-氯胺酮能减少慢性应激大鼠的不动时间。结论:两种氯胺酮对映体对大鼠睡眠-觉醒结构和行为的影响在相同剂量下有显著差异。(S) -氯胺酮显著影响睡眠-觉醒周期,很可能影响睡眠相关的神经可塑性,这可能与其抗抑郁疗效有关。我们关于(R)-氯胺酮对警惕性和行为缺乏影响的结果与最近的临床研究一致。
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来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
期刊介绍: The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.
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