TY - JOUR
T1 - Effect of short-term intralipid infusion on the immune response during low-dose endotoxemia in humans
AU - Krogh-Madsen, Rikke
AU - Plomgaard, Peter
AU - Akerstrom, Thorbjorn
AU - Møller, Kirsten
AU - Schmitz, Ole
AU - Pedersen, Bente Klarlund
PY - 2008/2
Y1 - 2008/2
N2 - Novel anti-inflammatory effects of insulin have recently been described, and insulin therapy to maintain euglycemia suppresses the plasma levels of free fatty acids (FFA) and increases the survival of critically ill patients. We aimed to explore the effect of short-term high levels of plasma FFA on the inflammatory response to a low dose of endotoxin. Fourteen healthy male volunteers underwent the following two trials in a randomized crossover design: 1) continuous infusion of 20% Intralipid [0.7 ml.kg(-1).h(-1) (1.54 g/kg)] for 11 h, and 2) infusion of isotonic saline for 11 h (control). In each trial, heparin was given to activate lipoprotein lipase, and an intravenous bolus of endotoxin (0.1 ng/kg) was given after 6 h of Intralipid/saline infusion. Blood samples and muscle and fat biopsies were obtained before the Intralipid/saline infusion and before as well as after infusion of an endotoxin bolus. Plasma levels of FFA, triglycerides, and glycerol were markedly increased during the Intralipid infusion. Endotoxin exposure induced an increase in plasma levels of TNF-alpha, IL-6, and neutrophils and further stimulated gene expression of TNF-alpha and IL-6 in both skeletal muscle and adipose tissue. The systemic inflammatory response to endotoxin was significantly pronounced during Intralipid infusion. Short-term hyperlipidemia enhances the inflammatory response to endotoxin, and skeletal muscle and adipose tissue are capable of producing essential inflammatory mediators after endotoxin stimulation.
AB - Novel anti-inflammatory effects of insulin have recently been described, and insulin therapy to maintain euglycemia suppresses the plasma levels of free fatty acids (FFA) and increases the survival of critically ill patients. We aimed to explore the effect of short-term high levels of plasma FFA on the inflammatory response to a low dose of endotoxin. Fourteen healthy male volunteers underwent the following two trials in a randomized crossover design: 1) continuous infusion of 20% Intralipid [0.7 ml.kg(-1).h(-1) (1.54 g/kg)] for 11 h, and 2) infusion of isotonic saline for 11 h (control). In each trial, heparin was given to activate lipoprotein lipase, and an intravenous bolus of endotoxin (0.1 ng/kg) was given after 6 h of Intralipid/saline infusion. Blood samples and muscle and fat biopsies were obtained before the Intralipid/saline infusion and before as well as after infusion of an endotoxin bolus. Plasma levels of FFA, triglycerides, and glycerol were markedly increased during the Intralipid infusion. Endotoxin exposure induced an increase in plasma levels of TNF-alpha, IL-6, and neutrophils and further stimulated gene expression of TNF-alpha and IL-6 in both skeletal muscle and adipose tissue. The systemic inflammatory response to endotoxin was significantly pronounced during Intralipid infusion. Short-term hyperlipidemia enhances the inflammatory response to endotoxin, and skeletal muscle and adipose tissue are capable of producing essential inflammatory mediators after endotoxin stimulation.
KW - Adipose Tissue/drug effects
KW - Adult
KW - Blood Cell Count
KW - Cross-Over Studies
KW - Cytokines/biosynthesis
KW - Endotoxemia/immunology
KW - Fat Emulsions, Intravenous/administration & dosage
KW - Fatty Acids, Nonesterified/metabolism
KW - Glucose/metabolism
KW - Humans
KW - Immunity/drug effects
KW - Inflammation/pathology
KW - Infusions, Intravenous
KW - Leukocyte Count
KW - Lipid Metabolism/drug effects
KW - Lipopolysaccharide Receptors/metabolism
KW - Male
KW - Monocytes
KW - Muscle, Skeletal/drug effects
KW - Neutrophils/drug effects
KW - RNA/biosynthesis
KW - Reverse Transcriptase Polymerase Chain Reaction
U2 - 10.1152/ajpendo.00507.2007
DO - 10.1152/ajpendo.00507.2007
M3 - Journal article
C2 - 18056792
SN - 0193-1849
VL - 294
SP - E371-9
JO - American Journal of Physiology: Endocrinology and Metabolism
JF - American Journal of Physiology: Endocrinology and Metabolism
IS - 2
ER -