CHANGES IN OXYGEN-CONSUMPTION RELATIVE TO OXYGEN DELIVERY IN ENDOTOXEMIC DOGS GIVEN ADRENERGIC AGENTS

Citation
Pd. Hansen et al., CHANGES IN OXYGEN-CONSUMPTION RELATIVE TO OXYGEN DELIVERY IN ENDOTOXEMIC DOGS GIVEN ADRENERGIC AGENTS, The Journal of surgical research, 57(1), 1994, pp. 156-163
Citations number
32
Categorie Soggetti
Surgery
ISSN journal
00224804
Volume
57
Issue
1
Year of publication
1994
Pages
156 - 163
Database
ISI
SICI code
0022-4804(1994)57:1<156:CIORTO>2.0.ZU;2-0
Abstract
Adrenergic agents (AAs) have been used in critically ill patients to i ncrease oxygen delivery (DO2). Associated parallel increases in oxygen consumption (VO2) have been noted and are thought to represent improv ed tissue oxygen utilization at supraphysiologic levels of DO2. We hyp othesize that the increase in VO2 associated with the use of AAs in se ptic animals is secondary to direct, obligate, metabolic effects of th e agents themselves. In this study, mongrel dogs were anesthetised, pa ralyzed, and had minimum temperature maintained on a warming blanket. Pulmonary and systemic hemodynamics were monitored. DO2 was calculated , while VO2 was measured directly with a metabolic cart. All dogs were given an Escherichia coli challenge and a colloid fluid resuscitation . Two hours after the onset of endotoxemia, baseline values were obtai ned, followed by four progressively larger doses of saline, dobutamine , or dopamine. At each dose there was a 40-min stabilization period an d a 20-min measurement of hemodynamics and VO2. Data were analyzed usi ng analysis of variance with a Scheffe's S test. P values of <0.05 wer e considered significant. The control group slowly decreased VO2 durin g the 6-hr experiment to 73% of baseline. Dobutamine increased VO2 to 119% of baseline (31% above control) and dopamine to 111% of baseline (28% over control). We conclude that adrenergic agents cause a signifi cant increase in whole body VO2 at moderate doses in septic dogs. It i s likely, therefore, that the ''pathologic'' relationship between VO2 and DO2 described in critically ill patients is partially due to the d irect metabolic effects of AAs. (C) 1994 Academic Press, Inc.