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Surg Infect (Larchmt) ; 16(1): 90-6, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25651466

ABSTRACT

BACKGROUND: Hyperglycemia associated with insulin resistance is common among critically ill patients. Interleukin (IL)-18 has been linked with hyperglycemia and insulin resistance in chronic disease, but the relation between IL-18 and insulin resistance during critical illness was unexplored. This study investigated whether IL-18 modulates hyperglycemia and insulin resistance during acute inflammation. METHODS: We injected lipopolysaccharide (LPS) 40 mg/kg into wild-type (WT) and IL-18 knockout (KO) mice to induce endotoxemia and examined insulin resistance and insulin-dependent signaling pathways during the acute phase. RESULTS: During the first hour after LPS treatment, IL-18 KO mice showed higher blood glucose and insulin and less insulin receptor substrate-1 and less phosphorylated Akt in the liver compared with WT mice. Interleukin-18 KO mice exhibited better survival after LPS treatment. CONCLUSIONS: The findings suggest that endogenous IL-18 may attenuate hyperglycemia and modulate insulin signaling in liver. Accordingly, IL-18 may modulate glucose tolerance during acute inflammation.


Subject(s)
Endotoxemia/complications , Endotoxemia/physiopathology , Hyperglycemia/complications , Hyperglycemia/physiopathology , Hyperinsulinism/complications , Hyperinsulinism/physiopathology , Interleukin-18/metabolism , Animals , Endotoxemia/chemically induced , Insulin Resistance , Interleukin-18/genetics , Lipopolysaccharides/administration & dosage , Lipopolysaccharides/toxicity , Liver/pathology , Male , Mice, Inbred C57BL , Mice, Knockout , Signal Transduction
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