Feingold A, Holaday D A
Br J Anaesth. 1977 Feb;49(2):155-62. doi: 10.1093/bja/49.2.155.
The non-steady state metabolism of inhalation anaesthetics during anaesthesia and recovery was simulated with a linear and non-linear whole body compartmental model. These two models were studied for nine anaesthetics during 1-MAC anaesthesias lasting 1, 4 and 8 h and recovery from 5 to 10 days. Both models demonstrated significant metabolism for several days following anaesthesia. For the linear model, both the percentage and the molar quantity of anaesthetic metabolized increased with increased duration of anaesthesia, increased anaesthetic fat solubility and increased assumed rate of hepatic metabolism. For the non-linear model, the duration of anaesthesia had little effect on the percentage metabolized but demonstrated increased molar quantities of anaesthetic metabolized with increased duration of anaesthesia and increased fat solubility. The agreement between the results obtained from the non-linear model and experimental data in the literature suggests that many inhalation anaesthetics belong to a class of xenobiotics whose biotransformation is limited by the same or similar non-linear rate-limiting step(s). A difference in the quantities of anaesthetic metabolized would be a direct consequence of the tissue solubilities of the anaesthetic.
采用线性和非线性全身房室模型模拟麻醉和苏醒过程中吸入麻醉药的非稳态代谢。在持续1、4和8小时的1-MAC麻醉以及5至10天的苏醒过程中,对这两种模型的9种麻醉药进行了研究。两种模型均显示麻醉后数天存在显著代谢。对于线性模型,麻醉药代谢的百分比和摩尔量均随麻醉持续时间的延长、麻醉药脂溶性的增加以及假定的肝代谢速率的增加而增加。对于非线性模型,麻醉持续时间对代谢百分比影响不大,但显示随着麻醉持续时间的延长和脂溶性的增加,麻醉药代谢的摩尔量增加。非线性模型所得结果与文献中的实验数据之间的一致性表明,许多吸入麻醉药属于一类外源性物质,其生物转化受相同或相似的非线性限速步骤限制。麻醉药代谢量的差异将是麻醉药组织溶解度的直接结果。