British Journal of Anaesthesia, Vol 81, Issue 5 761-765, Copyright © 1998 by The Board of Management and Trustees of the British Journal of Anaesthesia
T. Tsubokawa, K. Yamamoto, K. Nishimura, T. Yagi and T. Kobayashi
We have investigated the effect of inhaled oxygen tension on lipid
metabolism during propofol infusion. Propofol is supplied as a lipid
emulsion containing 10% soybean oil, which is rich in triglycerides (TG).
Infused TG are metabolized via three pathways in the liver cell; Krebs
cycle, ketogenesis and release as very low density lipoproteins (VLDL) into
the blood. For this reason, we measured TG and the products of the three
pathways; carbon dioxide, ketone bodies and VLDL. Thirty- two rabbits were
anaesthetized under four different conditions: propofol under hyperoxia,
normoxia, hypoxia and isoflurane anaesthesia under hyperoxia. Our results
indicated that hyperoxia produced more ketone bodies, normoxia more PaCO2
and hypoxia more free fatty acids (FFA) and TG compared with the other
propofol infusion groups. We conclude that hyperoxia during propofol
infusion facilitated fat metabolism through ketogenesis, while normoxia did
so via the Krebs cycle. Also, hypoxia suppressed utilization of TG and VLDL
production in the liver.
LABORATORY INVESTIGATIONS
Effects of inhaled oxygen concentration on fat metabolism during propofol infusion in rabbits
Department of Anaesthesiology and Intensive Care Medicine, School of Medicine, Faculty of Medicine, Kanazawa University, Takara-machi 13-1, Kanazawa 920-8641, Japan
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