Endotoxin-induced changes in IGF-I differ in rats provided enteral vs. parenteral nutrition

Am J Physiol. 1999 Mar;276(3):E455-64. doi: 10.1152/ajpendo.1999.276.3.E455.

Abstract

The purpose of the present study was to determine whether acute changes in the insulin-like growth factor (IGF) system induced by mild surgical trauma/fasting or endotoxin [lipopolysaccharide (LPS)] are differentially modulated by total enteral nutrition (TEN) or total parenteral nutrition (TPN). Rats had vascular catheters and a gastrostomy tube surgically placed and were fasted overnight. The next morning animals randomly received an isocaloric, isonitrogenous (250 kcal. kg-1. day-1, 1.6 g N. kg-1. day-1) infusion of either TEN or TPN for 48 h. Then rats were injected intravenously with Escherichia coli LPS (1 mg/kg) while nutritional support was continued. Time-matched control animals were injected with saline. After mild surgical trauma and an 18-h fast, TEN was more effective at increasing plasma IGF-I levels than TPN. Subsequent injection of LPS decreased IGF-I in blood, liver, and muscle in both TEN- and TPN-fed rats compared with saline-injected control animals. However, this decrease was approximately 30% greater in rats fed TPN compared with those fed TEN. LPS-induced downregulation of IGF-I mRNA expression in liver and muscle was also more prominent in TPN-fed rats. The LPS-induced increase in plasma corticosterone and tumor necrosis factor-alpha was greater (2- and 1.6-fold, respectively) in TPN-fed rats, and these changes were consistent with the greater reduction in IGF-I seen in these animals. In similarly treated rats allowed to survive for 24 h after LPS injection, the LPS-induced increase in the urinary 3-methylhistidine-to-creatinine ratio was smaller in TEN-fed rats. In summary, LPS reduced systemic levels of IGF-I as well as IGF-I protein and mRNA in critical target organs. Enteral feeding greatly attenuated this response. Maintenance of higher IGF-I levels in TEN-fed rats was associated with a reduction in inflammatory cytokine levels and lower rates of myofibrillar degradation.

Publication types

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

MeSH terms

  • Animals
  • Blood Glucose / analysis
  • Body Weight / physiology
  • Creatinine / urine
  • Endotoxins / pharmacology*
  • Enteral Nutrition*
  • Hormones / blood
  • Insulin-Like Growth Factor Binding Protein 1 / blood
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism*
  • Male
  • Methylhistidines / urine
  • Osmolar Concentration
  • Parenteral Nutrition*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Triglycerides / blood
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Blood Glucose
  • Endotoxins
  • Hormones
  • Insulin-Like Growth Factor Binding Protein 1
  • Methylhistidines
  • RNA, Messenger
  • Triglycerides
  • Tumor Necrosis Factor-alpha
  • Insulin-Like Growth Factor I
  • Creatinine
  • 3-methylhistidine