Publication | Open Access
Increased sheep lung vascular permeability caused by Escherichia coli endotoxin.
360
Citations
15
References
1979
Year
Acute Lung InjuryLung InflammationVeterinary MicrobiologyPseudomonas BacteriaBacterial PathogensSteady StateEscherichia Coli EndotoxinSepsisInfection ControlMicrobial ToxinPulmonary CirculationVascular BiologyClinical MicrobiologyPulmonary Vascular DiseasePulmonary Arterial HypertensionMicrobial DiseasePathogenesisEndothelial DysfunctionVeterinary ScienceMicrobiologyMedicine
We infused Escherichia coli endotoxin, 0.07-1.33 microgram/kg, intravenously into chronically instrumented unanesthetized sheep and measured pulmonary arterial and left atrial pressures, lung lymph flow, lymph and blood plasma protein concentrations, and arterial blood gases. Endotoxin caused a biphasic reaction: an early phase of pulmonary hypertension and a long late phase of steady state increased pulmonary vascular permeability during which pulmonary arterial and left atrial pressures were not increased significantly and lung lymph flow was 5 times the baseline value. Lymph: plasma total protein concentration ratio during the late phase (0.76 +/- 0.04) was significantly (P less than 0.05) higher than during baseline (0.66 +/- 0.03). The lymph response was reproducible. Lung lymph clearance of endogenous proteins with molecular radii (r) 35.5 to 96 A was increased during the steady state late phase of the reaction, but, as during baseline, clearance decreased as r increased. The endotoxin reaction was similar to the reaction to infusing whole Pseudomonas bacteria, except that endotoxin had less effect on pressures during the steady state response and caused a relatively larger increase in lymph clearance of large proteins. We conclude that E. coli endotoxin in sheep causes a long period of increased lung vascular permeability and may have a greater effect on large solute pathways across microvessels than do Pseudomonas bacteria.
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