Effects of systemic infusions of endotoxin, tumor necrosis factor, and interleukin-1 on glucose metabolism in the rat: relationship to endogenous glucose production and peripheral tissue glucose uptake

Metabolism. 1994 Mar;43(3):279-84. doi: 10.1016/0026-0495(94)90093-0.

Abstract

This study was performed to characterize and compare the actions of insulin on hepatic glucose production and peripheral glucose utilization during infusions of endotoxin, tumor necrosis factor (TNF), interleukin-1 (IL-1), and a combination of IL-1 and TNF in the rat. The euglycemic hyperinsulinemic clamp technique was combined with a primed-constant tracer infusion of high-performance liquid chromatography (HPLC)-purified 3H-3-glucose for estimation of whole-body glucose appearance and utilization rates; 14C-deoxyglucose (14C-DG) uptake was also measured in specific tissues following intravenous bolus administration. As expected, acute endotoxemia resulted in a significant reduction of glucose infusion during the clamp procedure (insulin concentration, 100 microU/mL), suggesting decreased insulin action. Similarly, infusion of TNF decreased the rate of glucose infusion necessary to maintain euglycemia. However, differences between endotoxin- and cytokine-treated rats were noted in whole-body glucose appearance (or disappearance) rates. Whereas endotoxin infusion predominantly decreased whole-body glucose uptake, suggesting diminished utilization in skeletal muscles, cytokine infusions were associated with a measurable hepatic glucose output despite hyperinsulinemia. In contrast, both cytokine and endotoxin administration decreased the rate of 14C-DG uptake by muscle tissue. These results demonstrate that TNF, IL-1, and endotoxin can induce a state of insulin resistance when infused continuously; the results also emphasize the complexity of regulation of glucose homeostasis during infection and sepsis.

Publication types

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

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • Deoxyglucose / administration & dosage
  • Endotoxins / administration & dosage
  • Endotoxins / pharmacology*
  • Glucose / metabolism*
  • Glucose / pharmacokinetics*
  • Infusions, Intravenous
  • Injections, Intravenous
  • Insulin / physiology
  • Insulin Resistance / physiology
  • Interleukin-1 / administration & dosage
  • Interleukin-1 / pharmacology*
  • Liver / metabolism
  • Male
  • Muscles / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Tritium
  • Tumor Necrosis Factor-alpha / administration & dosage
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Endotoxins
  • Insulin
  • Interleukin-1
  • Tumor Necrosis Factor-alpha
  • Tritium
  • Deoxyglucose
  • Glucose