Avram M J, Krejcie T C, Niemann C U, Enders-Klein C, Shanks C A, Henthorn T K
Department of Anesthesiology, Northwestern University Medical School, Chicago, Illinois 60611-3008, USA.
Anesthesiology. 2000 Jun;92(6):1757-68. doi: 10.1097/00000542-200006000-00036.
Earlier studies have demonstrated that physiologic marker blood concentrations in the first minutes after administration, when intravenous anesthetics exert their maximum effect, are determined by both cardiac output and its distribution. Given the reported vasodilating properties of isoflurane, we studied the effects of isoflurane anesthesia on marker disposition as another paradigm of altered cardiac output and regional blood flow distribution.
The dispositions of markers of intravascular space and blood flow (indocyanine green), extracellular space and free water diffusion (inulin), and total body water and tissue perfusion (antipyrine) were determined in four purpose-bred coonhounds. The dogs were studied while awake and while anesthetized with 1.7%, 2.6%, and 3.5% isoflurane (1.15, 1.7, and 2.3 minimum alveolar concentration, respectively) in a randomized order determined by a Latin square experimental design. Marker dispositions were described by recirculatory pharmacokinetic models based on very frequent early, and less frequent later, arterial blood samples. These models characterize the role of cardiac output and regional blood flow distribution on drug disposition.
Isoflurane caused a significant and dose-dependent decrease in cardiac output. Antipyrine disposition was profoundly affected by isoflurane anesthesia, during which nondistributive blood flow was maintained despite decreases in cardiac output, and the balance between fast and slow tissue volumes and blood flows was altered.
The isoflurane-induced changes in marker disposition were different than those the authors reported previously for halothane anesthesia, volume loading, or hypovolemia. These data provide further evidence that not only cardiac output but also its peripheral distribution affect early drug concentration history after rapid intravenous administration.
早期研究表明,静脉麻醉药发挥最大作用后的最初几分钟内,生理标志物的血药浓度由心输出量及其分布共同决定。鉴于异氟烷具有血管舒张特性,我们研究了异氟烷麻醉对标志物处置的影响,以此作为心输出量和局部血流分布改变的另一种范例。
在四只专门培育的猎浣熊犬中测定血管内空间和血流标志物(吲哚菁绿)、细胞外空间和自由水扩散标志物(菊粉)以及总体水和组织灌注标志物(安替比林)的处置情况。按照拉丁方实验设计确定的随机顺序,在犬清醒时以及用1.7%、2.6%和3.5%异氟烷麻醉时(分别为1.15、1.7和2.3最低肺泡浓度)对其进行研究。基于非常频繁的早期和较少频繁的后期动脉血样本,用再循环药代动力学模型描述标志物处置情况。这些模型表征了心输出量和局部血流分布在药物处置中的作用。
异氟烷导致心输出量显著且呈剂量依赖性降低。安替比林的处置受到异氟烷麻醉的深刻影响,在此期间,尽管心输出量降低,但非分布性血流得以维持,且快速和慢速组织容积与血流之间的平衡发生了改变。
异氟烷引起的标志物处置变化与作者先前报道的氟烷麻醉、容量负荷或血容量不足引起的变化不同。这些数据进一步证明,不仅心输出量,而且其外周分布也会影响快速静脉给药后早期药物浓度变化过程。