Anesthesiology. 2021 Jan 1;134(1):35-51. doi: 10.1097/ALN.0000000000003590.
γ-Aminobutyric acid type A (GABAA) receptor agonists are known to cause involuntary muscle movements. The mechanism of these movements is not known, and its relationship to depth of anesthesia monitoring is unclear. We have explored the effect of involuntary muscle movement on the pharmacokinetic-pharmacodynamic model for the GABAA receptor agonist ABP-700 and its effects on the Bispectral Index (BIS) as well as the Modified Observer's Assessment of Alertness/Sedation (MOAA/S) scores.
Observations from 350 individuals (220 men, 130 women) were analyzed, comprising 6,312 ABP-700 concentrations, 5,658 ABP-700 metabolite (CPM-acid) concentrations, 25,745 filtered BIS values, and 6,249 MOAA/S scores, and a recirculatory model developed. Various subject covariates and pretreatment with an opioid or a benzodiazepine were explored as covariates. Relationships between BIS and MOAA/S models and involuntary muscle movements were examined.
The final model shows that the pharmacokinetics of ABP-700 are characterized by small compartmental volumes and rapid clearance. The BIS model incorporates an effect-site for BIS suppression and a secondary excitatory/disinhibitory effect-site associated with a risk of involuntary muscle movements. The secondary effect-site has a threshold that decreases with age. The MOAA/S model did not show excitatory effects.
The GABAA receptor agonist ABP-700 shows the expected suppressive effects for BIS and MOAA/S, but also disinhibitory effects for BIS associated with involuntary muscle movements and reduced by pretreatment. Our model provides information about involuntary muscle movements that may be useful to improve depth of anesthesia monitoring for GABAA receptor agonists.
γ-氨基丁酸 A 型(GABAA)受体激动剂已知会引起不自主的肌肉运动。其运动机制尚不清楚,与麻醉深度监测的关系也不清楚。我们已经探讨了不自主肌肉运动对 GABAA 受体激动剂 ABP-700 的药代动力学-药效学模型的影响,以及对双频谱指数(BIS)和改良的观察者评估的警觉/镇静评分(MOAA/S)的影响。
分析了 350 名个体(220 名男性,130 名女性)的观察结果,包括 6312 个 ABP-700 浓度、5658 个 ABP-700 代谢物(CPM-酸)浓度、25745 个过滤 BIS 值和 6249 个 MOAA/S 评分,并开发了一个再循环模型。探索了各种受试者协变量和阿片类药物或苯二氮䓬类药物的预处理作为协变量。检查了 BIS 和 MOAA/S 模型与不自主肌肉运动之间的关系。
最终模型表明,ABP-700 的药代动力学特征是小隔室体积和快速清除。BIS 模型包含一个 BIS 抑制的效应部位和一个与不自主肌肉运动相关的继发性兴奋性/抑制性效应部位,其风险与不自主肌肉运动相关。第二个效应部位的阈值随年龄降低。MOAA/S 模型没有显示出兴奋作用。
GABAA 受体激动剂 ABP-700 对 BIS 和 MOAA/S 显示出预期的抑制作用,但也对 BIS 产生抑制作用,与不自主肌肉运动有关,并在预处理时减少。我们的模型提供了与不自主肌肉运动相关的信息,这可能有助于改善 GABAA 受体激动剂的麻醉深度监测。