Manduca Joshua D, Thériault Rachel-Karson, Williams Olivia O F, Rasmussen Duncan J, Perreault Melissa L
Department of Molecular and Cellular Biology, University of Guelph (ON), Canada.
Department of Molecular and Cellular Biology, University of Guelph (ON), Canada; Collaborative Neuroscience Program, University of Guelph (ON), Canada.
Neuroscience. 2020 Aug 10;441:161-175. doi: 10.1016/j.neuroscience.2020.05.012. Epub 2020 May 15.
Ketamine is a promising therapeutic for treatment-resistant depression (TRD) but is associated with an array of short-term psychomimetic side-effects. These disparate drug effects may be elicited through the modulation of neural circuit activity. The purpose of this study was to therefore delineate dose- and time-dependent changes in ketamine-induced neural oscillatory patterns in regions of the brain implicated in depression. Wistar-Kyoto rats were used as a model system to study these aspects of TRD neuropathology whereas Wistar rats were used as a control strain. Animals received a low (10 mg/kg) or high (30 mg/kg) dose of ketamine and temporal changes in neural oscillatory activity recorded from the prefrontal cortex (PFC), cingulate cortex (Cg), and nucleus accumbens (NAc) for ninety minutes. Effects of each dose of ketamine on immobility in the forced swim test were also evaluated. High dose ketamine induced a transient increase in theta power in the PFC and Cg, as well as a dose-dependent increase in gamma power in these regions 10-min, but not 90-min, post-administration. In contrast, only low dose ketamine normalized innate deficits in fast gamma coherence between the NAc-Cg and PFC-Cg, an effect that persisted at 90-min post-injection. These low dose ketamine-induced oscillatory alterations were accompanied by a reduction in immobility time in the forced swim test. These results show that ketamine induces time-dependent effects on neural oscillations at specific frequencies. These drug-induced changes may differentially contribute to the psychomimetic and therapeutic effects of the drug.
氯胺酮是治疗难治性抑郁症(TRD)的一种有前景的疗法,但会伴有一系列短期拟精神病副作用。这些不同的药物效应可能是通过调节神经回路活动引发的。因此,本研究的目的是描绘氯胺酮诱导的与抑郁症相关的脑区神经振荡模式的剂量和时间依赖性变化。将Wistar-Kyoto大鼠用作模型系统来研究TRD神经病理学的这些方面,而将Wistar大鼠用作对照品系。动物接受低剂量(10mg/kg)或高剂量(30mg/kg)的氯胺酮,并记录前额叶皮质(PFC)、扣带皮质(Cg)和伏隔核(NAc)在90分钟内神经振荡活动的时间变化。还评估了各剂量氯胺酮对强迫游泳试验中不动时间的影响。高剂量氯胺酮在给药后10分钟而非90分钟诱导PFC和Cg中θ功率短暂增加,以及这些区域中γ功率的剂量依赖性增加。相比之下,只有低剂量氯胺酮使NAc-Cg和PFC-Cg之间快速γ相干性的先天缺陷恢复正常,这种效应在注射后90分钟持续存在。这些低剂量氯胺酮诱导的振荡改变伴随着强迫游泳试验中不动时间的减少。这些结果表明,氯胺酮对特定频率的神经振荡具有时间依赖性效应。这些药物诱导的变化可能对药物的拟精神病和治疗效果有不同的贡献。