Increased ileal-mucosal-arterial PCO2 gap is associated with impaired villus microcirculation in endotoxic pigs

Intensive Care Med. 2001 Apr;27(4):757-66. doi: 10.1007/s001340100871.

Abstract

Objective: To investigate whether an increased ileal-mucosal-arterial PCO2 gap (delta PCO2) during hyperdynamic porcine endotoxemia is associated with impaired villus microcirculation.

Design: Prospective, randomized, controlled, experimental study.

Setting: Animal research laboratory.

Animals: Twenty-two domestic pigs.

Interventions: After baseline measurements, anesthetized and ventilated pigs received continuous i.v. endotoxin (ETX, n = 12) for 24 h or placebo (SHAM, n = 10).

Measurements and results: Before, as well as 12 and 24 h after, the start of endotoxin or saline portal venous blood flow (QPV, ultrasound flow probe) and lactate/pyruvate ratios (L/P), the ileal-mucosal-arterial delta PCO2 (fiberoptic sensor) and bowel-wall capillary hemoglobin O2 saturation (%Hb-O2-cap, remission spectrophotometry) were assessed together with intravital video records of the ileal-mucosal microcirculation (number of perfused/heterogeneously perfused/unperfused villi) using orthogonal polarization spectral imaging (CYTOSCAN A/R) via an ileostomy. At 12 and 24 h endotoxin infusion, about half of the evaluated villi were heterogeneously or unperfused which was paralleled by a progressive significant increase of the ileal-mucosal-arterial delta PCO2 and portal venous L/P ratios, whereas QPV as well as both the mean %Hb-O2-cap and the %Hb-O2-cap frequency distributions remained unchanged. By contrast, in the SHAM-group, mucosal microcirculation was well-preserved, and none of the other parameters were influenced.

Conclusions: We conclude that an increased ileal-mucosal-arterial delta PCO2 during porcine endotoxemia is related to impaired villus microcirculation. A putative contribution of disturbed cellular oxygen utilization resulting from "cytopathic hypoxia" may also assume importance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Gas Analysis
  • Carbon Dioxide / blood*
  • Disease Models, Animal
  • Endotoxemia / blood*
  • Endotoxemia / physiopathology*
  • Escherichia coli Infections / blood*
  • Escherichia coli Infections / physiopathology*
  • Female
  • Ileum / blood supply*
  • Ileum / physiopathology*
  • Intestinal Mucosa / blood supply*
  • Intestinal Mucosa / physiopathology*
  • Lactic Acid / blood
  • Male
  • Mesenteric Arteries / physiopathology*
  • Microcirculation / physiopathology
  • Microscopy, Polarization
  • Portal Vein / physiopathology
  • Prospective Studies
  • Pyruvic Acid / blood
  • Spectrophotometry
  • Swine

Substances

  • Carbon Dioxide
  • Lactic Acid
  • Pyruvic Acid