Norepinephrine and N(G)-monomethyl-L-arginine in hyperdynamic septic shock in pigs: effects on intestinal oxygen exchange and energy balance.

Abstract

OBJECTIVES:

To compare the effects of norepinephrine (NOR) and the nonselective nitric oxide synthase inhibitor, N(G)-monomethyl-L-arginine (L-NMMA), on intestinal blood flow, oxygen exchange, and energy metabolism over 24 hrs of hyperdynamic, normotensive porcine endotoxic shock.

DESIGN:

Prospective, randomized, experimental study with repeated measures.

SETTING:

Investigational animal laboratory.

SUBJECTS:

Twenty-seven pigs were divided into three groups: seven animals received no vasopressor therapy (ETX) during endotoxic shock; ten animals were treated with NOR; and ten animals were treated with L-NMMA.

INTERVENTIONS:

Pigs were anesthetized, mechanically ventilated, and instrumented. Eight hours later, endotoxic shock was initiated by an infusion of Escherichia coli lipopolysaccharide. Animals were resuscitated by hetastarch directed to maintain the intrathoracic blood volume and a mean arterial pressure (MAP) of >60 mm Hg. Twelve hours after the start of the endotoxin infusion, NOR or L-NMMA was administered for 12 hrs in the treatment groups to maintain a MAP at preshock levels.

MEASUREMENTS AND MAIN RESULTS:

ETX caused a continuous fall in MAP, despite a sustained increase in the cardiac output achieved by fluid resuscitation. NOR maintained MAP at preshock levels because of a further rise in cardiac output, whereas hemodynamic stabilization during L-NMMA resulted from systemic vasoconstriction. NOR increased portal venous blood flow concomitant with decreased intestinal oxygen extraction, whereas L-NMMA influenced neither portal venous blood flow nor intestinal oxygen extraction. Mean capillary hemoglobin oxygen saturation of the ileal mucosa as well as the frequency distributions reflecting microcirculatory oxygen availability remained unchanged as well. Nevertheless, portal venous pH similarly decreased and portal venous lactate/pyruvate ratios increased in all three groups. The arterial-ileal mucosal PCO2 gap progressively increased in the ETX and L-NMMA groups, whereas NOR blunted this response.

CONCLUSIONS:

Neither treatment could reverse the ETX-induced derangements of cellular energy metabolism as reflected by the increased portal venous lactate/pyruvate ratios. The NOR-induced attenuation of ileal mucosal acidosis was possibly caused by a different pattern of blood flow redistribution compared with L-NMMA.

• Authors: K Träger, P Radermacher, K M Rieger, R Grover, A Vlatten, T Iber, J Adler, M Georgieff, B Santak
• Journal: Critical care medicine (Crit Care Med) Vol. 28 Issue 6 Pg. 2007-14 (Jun 2000) ISSN: 0090-3493 [Print] United States
• PMID: 10890656 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Enzyme Inhibitors
• Vasoconstrictor Agents
• omega-N-Methylarginine
• Oxygen
• Norepinephrine

Topics

• Animals
• Energy Metabolism (drug effects)
• Enzyme Inhibitors (pharmacology)
• Female
• Intestinal Mucosa (metabolism)
• Intestines (drug effects)
• Male
• Norepinephrine (pharmacology)
• Oxygen (metabolism)
• Shock, Septic (metabolism)
• Swine
• Vasoconstrictor Agents (pharmacology)
• omega-N-Methylarginine (pharmacology)