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The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices

机译:全身麻醉丙泊酚诱导海马小鼠脑片样发作样发作

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摘要

The general anesthetic propofol has been in clinical use for more than 30 years and has become the agent of choice for rapid intravenous induction. While its hypnotic and anti-convulsant properties are well known, the propensity for propofol to promote seizure activity is less well characterised. Electroencephalogram-confirmed reports of propofol-induced seizure activity implicate a predisposition in epileptic subjects. The aim of this study was to investigate the seizure-promoting action of propofol in mouse brain slices—with the goal of establishing an in vitro model of propofol pro-convulsant action for future mechanistic studies. Coronal slices were exposed to either normal artificial cerebrospinal fluid (aCSF) or no-magnesium (no-Mg) aCSF—and extracellular field potential recordings made from the hippocampus, entorhinal cortex and neocortex. Propofol (and etomidate for comparison) were delivered at three stepwise concentrations corresponding to clinically relevant levels. The main finding was that propofol induced ictal-like seizures in seven out of ten hippocampal recordings (p = 0.004 compared to controls) following pre-exposure to no-Mg aCSF—but strongly inhibited seizure-like event (SLE) activity in the neocortex. Propofol did not induce seizure activity in slices exposed to normal aCSF. The results support the contention that propofol has the capacity to promote seizure activity, particularly when there is an underlying seizure predisposition. This study establishes an in vitro model for exploring the mechanisms by which propofol promotes subcortical seizure activity.
机译:全身麻醉丙泊酚已在临床上使用了30多年,并已成为快速静脉引产的首选药物。尽管其催眠和抗惊厥特性众所周知,但对异丙酚促进癫痫发作活性的倾向尚不十分清楚。脑电图证实丙泊酚诱导的癫痫发作活性暗示了癫痫患者的易感性。这项研究的目的是研究丙泊酚在小鼠脑片中的癫痫促进作用,目的是为将来的机理研究建立异丙酚促惊厥作用的体外模型。将冠状切片暴露于正常的人工脑脊液(aCSF)或无镁(no-Mg)aCSF,以及海马,内嗅皮层和新皮层的细胞外场电势记录。丙泊酚(与依托咪酯比较)以对应于临床相关水平的三个逐步浓度给药。主要发现是在无镁aCSF预先暴露后,异丙酚在十次海马记录中有七次诱发冰样样癫痫发作(与对照相比,p = 0.004),但强烈抑制了新皮层的癫痫样事件(SLE)活性。 。丙泊酚在暴露于正常aCSF的切片中不会诱导癫痫发作活性。该结果支持以下观点:丙泊酚具有促进癫痫发作活动的能力,尤其是在存在潜在的癫痫发作倾向时。这项研究建立了一个体外模型,以探索异丙酚促进皮层下癫痫发作活性的机制。

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