Beaufort A M, Wierda J M, Houwertjes M C, Kleef U W, Meijer D K
Research Group for Experimental Anesthesiology and Clinical Pharmacology, University of Groningen, The Netherlands.
J Pharmacol Toxicol Methods. 1993 Jun;29(3):147-56. doi: 10.1016/1056-8719(93)90066-n.
In the search for drugs with an extreme short time course of action, compounds should be developed that are rapidly distributed to and temporarily stored in well-perfused organs. Since the lungs receive the complete cardiac output and have the ability to temporarily store drugs, we have developed an in situ, isolated lung preparation in the cat to study the contribution of the lungs to the disposition of drugs. The cat's own heart perfuses the lung in situ with autologous blood. The circulation between the left ventricle and the right atrium is short-circuited via an aorta-caval shunt. The right forelimb is added to study pharmacodynamics simultaneously (only for muscle relaxants). Validation of the model for 180 min of perfusion showed complete isolation of the organs without major biochemical changes or edema and a stable muscle response. In pilot experiments with two structurally related muscle relaxants, initial muscle relaxation was followed by spontaneous recovery of neuromuscular function and a gradually decreasing plasma concentration, indicating partial disposition by the lungs. This was confirmed by direct concentration measurements in the lung. The present model may provide a powerful experimental tool to elucidate the role of the lungs in the disposition of drugs.
在寻找作用时间极短的药物时,应研发能迅速分布并暂时储存在灌注良好器官中的化合物。由于肺接受全部的心输出量且有暂时储存药物的能力,我们已开发出一种猫原位离体肺制备模型,以研究肺对药物处置的作用。猫自身的心脏用自体血液原位灌注肺。左心室与右心房之间的循环通过主动脉 - 腔静脉分流短路。添加右前肢以便同时研究药效学(仅用于肌肉松弛剂)。对灌注180分钟的模型进行验证显示,器官完全隔离,无重大生化变化或水肿,肌肉反应稳定。在使用两种结构相关的肌肉松弛剂进行的初步实验中,最初的肌肉松弛之后是神经肌肉功能的自发恢复以及血浆浓度逐渐降低,表明肺参与了部分处置过程。这通过对肺中药物浓度的直接测量得到了证实。本模型可能为阐明肺在药物处置中的作用提供一个强大的实验工具。