Transvisceral lactate fluxes during early endotoxemia

Chest. 1996 Jul;110(1):198-204. doi: 10.1378/chest.110.1.198.

Abstract

The pathogenesis of hyperlacticemia during sepsis is poorly understood. We investigated the role of lung, kidney, gut, liver, and muscle in endogenous lactate uptake and release during early endotoxemia in an intact, pentobarbital-anesthetized dog model (n = 14). Ultrasonic flow probes were placed around the portal vein and hepatic, renal, and femoral arteries. After splenectomy, catheters were inserted into the pulmonary artery, aorta, and hepatic, left renal, and femoral veins. Whole blood lactate and blood gases from all catheters, organ flows, and cardiac output were measured before and 30 to 45 min after a bolus infusion of Eacherichia coli endotoxin (1 mg/kg). After endotoxin infusion, mean arterial blood lactate level increased from 0.92 +/- 0.11 to 1.60 +/- 0.15 mmol/L (p < 0.0001). Lung lactate flux changed from uptake to release of lactate adding a mean of 9.97 +/- 16.23 mmol/h (p < 0.05) to the systemic circulation. Liver and muscle lactate fluxes remained neutral at all times, while kidney and gut took up lactate from the circulation both before and after endotoxin infusion (mean renal uptake, 2.73 +/- 3.85 mmol/L; p < 0.001; mean gut uptake, 2.46 +/- 2.31 mmol/h; p < 0.002). Except for the kidney, where a decrease in blood flow correlated with diminished uptake, there was no correlation between changes in transvisceral lactate fluxes and organ or systemic oxygen delivery during endotoxemia. A positive correlation between lactate uptake and oxygen consumption during endotoxemia was seen for both gut (p < 0.0001) and kidney (p < 0.002). We conclude that, in the dog, the pathogenesis of endotoxin-induced hyperlacticemia is complex. The lung may be responsible for significant lactate release, and other viscera that normally take up lactate are unable to adequately clear this increased lactate.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blood Flow Velocity
  • Cardiac Output
  • Dogs
  • Endotoxins / administration & dosage
  • Endotoxins / blood*
  • Escherichia coli
  • Hindlimb
  • Intestinal Mucosa / metabolism
  • Intestines / blood supply
  • Kidney / blood supply
  • Kidney / metabolism
  • Lactates / blood
  • Lactates / metabolism*
  • Lactic Acid
  • Liver / blood supply
  • Liver / metabolism
  • Lung / blood supply
  • Lung / metabolism
  • Male
  • Muscle, Skeletal / blood supply
  • Muscle, Skeletal / metabolism
  • Oxygen Consumption
  • Sepsis / metabolism

Substances

  • Endotoxins
  • Lactates
  • Lactic Acid