Armbruster K, Nöldge-Schomburg G F, Dressler I M, Fittkau A J, Haberstroh J, Geiger K
Department of Anesthesia, University Hospital, Freiburg, Germany.
Anesth Analg. 1997 Feb;84(2):271-7. doi: 10.1097/00000539-199702000-00007.
This study was designed to investigate the effects of desflurane on systemic and splanchnic hemodynamics, O2 delivery and O2 uptake, tissue oxygenation (as monitored by surface PO2 electrodes), and hepatic oxygen-dependent intermediary metabolism (hepatic lactate uptake, intestinal lactate production, ketone-body ratio) in the pig. We studied 11 anesthetized (i.e., ketamine, flunitrazepam, vecuronium) and ventilated domestic pigs (17-23 kg). After instrumentation, desflurane was administered randomly at 0.5 minimum alveolar anesthetic concentration (MAC) (4.2 vol %) and 1.0 MAC (8.3 vol %). Desflurane caused dose-dependent decreases in heart rate, mean arterial blood pressure, and cardiac output. Hepatic arterial blood flow was not affected at 0.5 MAC but decreased at 1.0 MAC. In contrast, portal and superior mesenteric arterial blood flow decreased at 0.5 MAC but did not show any further significant decrease at 1.0 MAC. Total hepatic blood flow decreased dose-dependently. Although O2 deliveries of whole body, liver, and small intestine were markedly reduced at both concentrations, respective O2 uptakes did not change significantly. The decreases in O2 deliveries were reflected by moderate disturbances in hepatic and small intestinal surface PO2. No evidence for severe tissue hypoxia could be detected. Desflurane had no adverse effects on hepatic and small intestinal metabolic function. These data indicate that hepatic and small intestinal O2 reserve capacity is impaired by desflurane.
本研究旨在探讨地氟醚对猪全身及内脏血流动力学、氧输送和氧摄取、组织氧合(通过表面PO2电极监测)以及肝脏氧依赖中间代谢(肝脏乳酸摄取、肠道乳酸生成、酮体比率)的影响。我们研究了11头麻醉(即氯胺酮、氟硝西泮、维库溴铵)并通气的家猪(17 - 23千克)。仪器安装后,随机给予地氟醚0.5最低肺泡有效浓度(MAC)(4.2体积%)和1.0 MAC(8.3体积%)。地氟醚导致心率、平均动脉血压和心输出量呈剂量依赖性降低。肝动脉血流在0.5 MAC时未受影响,但在1.0 MAC时降低。相反,门静脉和肠系膜上动脉血流在0.5 MAC时降低,但在1.0 MAC时未进一步显著降低。肝脏总血流量呈剂量依赖性降低。尽管两种浓度下全身、肝脏和小肠的氧输送均显著降低,但各自的氧摄取并未显著变化。氧输送的降低反映在肝脏和小肠表面PO2的中度紊乱上。未检测到严重组织缺氧的证据。地氟醚对肝脏和小肠代谢功能无不良影响。这些数据表明地氟醚损害了肝脏和小肠的氧储备能力。