Turku PET Centre, University of Turku and Turku University Hospital, Turku FI-20521, Finland.
Department of Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital, University of Turku, Turku FI-20521, Finland.
J Neurosci. 2023 Jun 28;43(26):4884-4895. doi: 10.1523/JNEUROSCI.2339-22.2023. Epub 2023 May 24.
Establishing the neural mechanisms responsible for the altered global states of consciousness during anesthesia and dissociating these from other drug-related effects remains a challenge in consciousness research. We investigated differences in brain activity between connectedness and disconnectedness by administering various anesthetics at concentrations designed to render 50% of the subjects unresponsive. One hundred and sixty healthy male subjects were randomized to receive either propofol (1.7 μg/ml; = 40), dexmedetomidine (1.5 ng/ml; = 40), sevoflurane (0.9% end-tidal; = 40), S-ketamine (0.75 μg/ml; = 20), or saline placebo ( = 20) for 60 min using target-controlled infusions or vaporizer with end-tidal monitoring. Disconnectedness was defined as unresponsiveness to verbal commands probed at 2.5-min intervals and unawareness of external events in a postanesthesia interview. High-resolution positron emission tomography (PET) was used to quantify regional cerebral metabolic rates of glucose (CMR) utilization. Contrasting scans where the subjects were classified as connected and responsive versus disconnected and unresponsive revealed that for all anesthetics, except S-ketamine, the level of thalamic activity differed between these states. A conjunction analysis across the propofol, dexmedetomidine and sevoflurane groups confirmed the thalamus as the primary structure where reduced metabolic activity was related to disconnectedness. Widespread cortical metabolic suppression was observed when these subjects, classified as either connected or disconnected, were compared with the placebo group, suggesting that these findings may represent necessary but alone insufficient mechanisms for the change in the state of consciousness. Experimental anesthesia is commonly used in the search for measures of brain function which could distinguish between global states of consciousness. However, most previous studies have not been designed to separate effects related to consciousness from other effects related to drug exposure. We employed a novel study design to disentangle these effects by exposing subjects to predefined EC doses of four commonly used anesthetics or saline placebo. We demonstrate that state-related effects are remarkably limited compared with the widespread cortical effects related to drug exposure. In particular, decreased thalamic activity was associated with disconnectedness with all used anesthetics except for S-ketamine.
确定麻醉状态下改变的意识全局状态的神经机制,并将其与其他与药物相关的效应区分开来,这仍然是意识研究中的一个挑战。我们通过给予不同浓度的麻醉剂来研究连通性和不连通性之间的大脑活动差异,这些浓度旨在使 50%的受试者无反应。160 名健康男性受试者被随机分为接受丙泊酚(1.7μg/ml;n=40)、右美托咪定(1.5ng/ml;n=40)、七氟醚(0.9%呼气末;n=40)、S-氯胺酮(0.75μg/ml;n=20)或生理盐水安慰剂(n=20)治疗 60 分钟,使用靶控输注或蒸发器进行呼气末监测。不连通性定义为每隔 2.5 分钟探测到的言语命令无反应和麻醉后访谈中对外界事件的无知。高分辨率正电子发射断层扫描(PET)用于定量区域性脑葡萄糖代谢率(CMR)利用。将受试者分类为连通和响应与不连通和无响应的对比扫描显示,除 S-氯胺酮外,所有麻醉剂的丘脑活动水平在这些状态之间存在差异。对丙泊酚、右美托咪定和七氟醚组进行的联合分析证实,丘脑是代谢活动减少与不连通性相关的主要结构。当将这些受试者,无论连通性或不连通性,与安慰剂组进行比较时,观察到广泛的皮质代谢抑制,表明这些发现可能代表意识状态变化的必要但单独不足的机制。实验性麻醉常用于寻找可区分意识全局状态的脑功能测量方法。然而,大多数先前的研究并未设计用于将与意识相关的效应与与药物暴露相关的其他效应分开。我们采用了一种新的研究设计,通过将受试者暴露于四种常用麻醉剂或生理盐水安慰剂的预设 EC 剂量来分离这些效应。我们证明,与药物暴露相关的广泛皮质效应相比,与状态相关的效应非常有限。特别是,除 S-氯胺酮外,所有使用的麻醉剂都与不连通性相关的丘脑活动减少有关。