Bailey J M
Department of Anesthesiology, Emory University School of Medicine, Atlanta, Georgia.
J Pharmacokinet Biopharm. 1989 Feb;17(1):109-23. doi: 10.1007/BF01059090.
The theoretical groundwork for a rate constant formulation of inhaled anesthetic elimination kinetics is discussed. In an effort to simulate recent experimental results a linear flow-limited five-compartment model was used comprising lung, vessel-rich tissue, muscle, nonvisceral fat, and an additional compartment, marrow-visceral fat whose functional existence recently has been experimentally demonstrated. Hypothetical but plausible parameters for the marrow-visceral fat compartment were used. The theoretically predicted values were in good agreement with experimental results suggesting that this model is appropriate for the elimination kinetics of agents that are not metabolized to any significant degree. Simple approximate expressions for the rate constants were also derived and were in reasonable agreement with experimental results. The model was also employed to clarify the effect of anesthetic duration on subsequent elimination kinetics.
讨论了吸入麻醉药消除动力学速率常数公式的理论基础。为了模拟最近的实验结果,使用了一个线性血流限制的五室模型,该模型包括肺、富血管组织、肌肉、非内脏脂肪和另一个室,即骨髓-内脏脂肪,其功能存在最近已通过实验证明。使用了骨髓-内脏脂肪室的假设但合理的参数。理论预测值与实验结果吻合良好,表明该模型适用于未发生显著代谢的药物的消除动力学。还推导了速率常数的简单近似表达式,且与实验结果合理吻合。该模型还用于阐明麻醉持续时间对后续消除动力学的影响。