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首页> 外文期刊>Molecular brain >Ketamine and its metabolite, (2R,6R)-HNK, restore hippocampal LTP and long-term spatial memory in the Wistar-Kyoto rat model of depression
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Ketamine and its metabolite, (2R,6R)-HNK, restore hippocampal LTP and long-term spatial memory in the Wistar-Kyoto rat model of depression

机译:氯胺酮及其代谢物,(2R,6R)-HNK,恢复海马LTP和Wistar-Kyoto大鼠抑郁型大鼠模型中的长期空间记忆

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Accumulating evidence implicates dysregulation of hippocampal synaptic plasticity in the pathophysiology of depression. However, the effects of ketamine on synaptic plasticity and their contribution to its mechanism of action as an antidepressant, are still unclear. We investigated ketamine’s effects on in vivo dorsal hippocampal (dHPC) synaptic plasticity and their role in mediating aspects of antidepressant activity in the Wistar-Kyoto (WKY) model of depression. dHPC long-term potentiation (LTP) was significantly impaired in WKY rats compared to Wistar controls. Importantly, a single low dose (5?mg/kg, ip) of ketamine or its metabolite, (2R,6R)-HNK, rescued the LTP deficit in WKY rats at 3.5?h but not 30?min following injection, with residual effects at 24?h, indicating a delayed, sustained facilitatory effect on dHPC synaptic plasticity. Consistent with the observed dHPC LTP deficit, WKY rats exhibited impaired hippocampal-dependent long-term spatial memory as measured by the novel object location recognition test (NOLRT), which was effectively restored by pre-treatment with both ketamine or (2R,6R)-HNK. In contrast, in WKYs, which display abnormal stress coping, ketamine, but not (2R,6R)-HNK, had rapid and sustained effects in the forced swim test (FST), a commonly used preclinical screen for antidepressant-like activity. The differential effects of (2R,6R)-HNK observed here reveal a dissociation between drug effects on FST immobility and dHPC synaptic plasticity. Therefore, in the WKY rat model, restoring dHPC LTP was not correlated with ketamine’s effects in FST, but importantly, may have contributed to the reversal of hippocampal-dependent cognitive deficits, which are critical features of clinical depression. Our findings support the theory that ketamine may reverse the stress-induced loss of connectivity in key neural circuits by engaging synaptic plasticity processes to “reset the system”.
机译:积累证据意味着在抑郁症病理生理学中的海马突触可塑性的失调。然而,氯胺酮对突触塑性的影响及其对其作为抗抑郁药的作用机制的贡献仍然尚不清楚。我们调查了氯胺酮对体内海马(DHPC)突触塑性的影响及其在Wistar-Kyoto(WKY)抑郁症模型中的抗抑郁活性方面的作用。与Wistar对照相比,WKY大鼠的DHPC长期增强(LTP)显着损害。重要的是,氯胺酮或其代谢物的单个低剂量(5?mg / kg,IP)(2r,6r)-hnk,在3.5℃下救出了WKY大鼠的LTP缺陷,但在注射后没有30?min,剩余在24℃下效果,表明对DHPC突触可塑性的延迟持续的促进作用。与观察到的DHPC LTP缺陷常规一致,WKY大鼠通过新的物体位置识别试验(NOLRT)测量而表现出的海马依赖性长期空间存储器受损,这通过用氯胺酮或(2R,6R)预处理有效地恢复-hnk。相比之下,在显示出异常应力应对,氯胺酮,但不是(2R,6R)-HNK中,在强制游泳试验(FST)中具有快速且持续的效果,常用的临床前筛网进行抗抑郁剂的活性。这里观察到的(2R,6R)-HNK的差异效应显示出对FST不动和DHPC突触可塑性的药物影响之间的解离。因此,在WKY大鼠模型中,恢复DHPC LTP与在FST中的氯胺酮的效果无关,但重要的是,可能导致海马依赖性认知缺陷的逆转,这是临床抑郁的关键特征。我们的研究结果支持通过将突触塑性过程与“重置系统复位”来“重置系统”来支持氯胺酮在关键神经电路中的应力引起的连接损失。

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