Metabolic, endocrine, and immune effects of stress hyperglycemia in a rabbit model of prolonged critical illness.

Stress hyperglycemia is frequent in critically ill patients. The aim of this study was to investigate the effect of blood glucose control with insulin on endocrine, metabolic, and immune function in an animal model of severe injury. Seventy-two hours after alloxan injection and exogenous insulin infusion combined with continuous iv parenteral nutrition, male New Zealand White rabbits received a burn injury and were allocated to a normoglycemic (n = 17) or hyperglycemic (n = 13) group. In the normoglycemic group, blood glucose levels were kept between 3.3 and 6.1 mmol/liter by insulin infusion, whereas in the hyperglycemic group blood glucose levels were maintained at 13.8-16.6 mmol/liter. Blood was drawn for biochemical analysis at regular time points. At 24 and 72 h after burn injury, immune function of monocytes was assessed in vitro. Maintenance of normoglycemia with exogenous insulin after severe trauma to a large extent prevented weight loss, lactic acidosis, and hyponatremia. Furthermore, within 3 d after injury, the intervention improved phagocytosis of monocytes investigated in fresh cells by more than a mean 150% (P = 0.006) and after 24-h incubation with or without lipopolysaccharide by more than a mean 4-fold (P = 0.001) and 2-fold (P = 0.05), respectively. Oxidative killing after 24-h incubation was also improved by 2-fold (P = 0.05), but no effect on chemotaxis was detected. Concomitantly, inflammation and stress-induced growth hormone hypersecretion were suppressed. Prevention of catabolism, acidosis, excessive inflammation, and impaired innate immune function may explain previously documented beneficial effects of intensive insulin therapy on outcome of critical illness.

[1]  R. Mindham,et al.  PARKINSONISM INDUCED BY FLUPHENAZINE DECANOATE , 1976, The Lancet.

[2]  R. Cooper,et al.  Euglycemic hyperinsulinemia augments the cytokine and endocrine responses to endotoxin in humans. , 2002, American journal of physiology. Endocrinology and metabolism.

[3]  G. Van den Berghe,et al.  A novel in vivo rabbit model of hypercatabolic critical illness reveals a biphasic neuroendocrine stress response. , 2002, Endocrinology.

[4]  A. Imrich,et al.  Immunologic effects of acute hyperglycemia in nondiabetic rats. , 1997, JPEN. Journal of parenteral and enteral nutrition.

[5]  N R Webster,et al.  Increased mortality associated with growth hormone treatment in critically ill adults. , 1999, The New England journal of medicine.

[6]  D. Chinkes,et al.  Anabolic Effects of Oxandrolone After Severe Burn , 2001, Annals of surgery.

[7]  D. Sodi-Pallares,et al.  Potassium, glucose, and insulin in myocardial infarction. , 1969, Lancet.

[8]  Y. Kaneda,et al.  Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage , 2000, Nature.

[9]  G. Berghe Dynamic neuroendocrine responses to critical illness , 2002, Frontiers in Neuroendocrinology.

[10]  C. Mathieu,et al.  In Vitro and In Vivo Analysis of the Immune System of Vitamin D Receptor Knockout Mice , 2001, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[11]  K. Federlin,et al.  Impairment of Polymorphonuclear Leukocyte Function and Metabolic Control of Diabetes , 1992, Diabetes Care.

[12]  K. Feingold,et al.  Infection and inflammation-induced proatherogenic changes of lipoproteins. , 2000, The Journal of infectious diseases.

[13]  L. Broemeling,et al.  Effects of recombinant human growth hormone on donor-site healing in severely burned children. , 1990, Annals of surgery.

[14]  Nielson Cp,et al.  Inhibition of Polymorphonuclear Leukocyte Respiratory Burst by Elevated Glucose Concentrations in Vitro , 1989 .

[15]  F. Zannad,et al.  Endothelial dysfunction and type 2 diabetes. Part 2: altered endothelial function and the effects of treatments in type 2 diabetes mellitus. , 2001, Diabetes & metabolism.

[16]  A. Aljada,et al.  Insulin Inhibits Intranuclear Nuclear Factor κB and Stimulates IκB in Mononuclear Cells in Obese Subjects: Evidence for an Anti-inflammatory Effect? , 2001 .

[17]  R. Kernohan,et al.  Potassium, glucose, and insulin in myocardial infarction. , 1967, Lancet.

[18]  C. Pison,et al.  Glucose modulates hemodynamic, metabolic, and inflammatory responses to lipopolysaccharide in rabbits. , 1997, Journal of applied physiology.

[19]  M. Saad,et al.  Insulin regulates plasma ghrelin concentration. , 2002, The Journal of clinical endocrinology and metabolism.

[20]  G. Van den Berghe,et al.  Intensive insulin therapy exerts antiinflammatory effects in critically ill patients and counteracts the adverse effect of low mannose-binding lectin levels. , 2003, The Journal of clinical endocrinology and metabolism.

[21]  D. Chinkes,et al.  Efficacy of a high-carbohydrate diet in catabolic illness , 2001, Critical care medicine.

[22]  M. Kasuga,et al.  Low phagocytic activity of resident peritoneal macrophages in diabetic mice: relevance to the formation of advanced glycation end products. , 1999, Diabetes.

[23]  G. Van den Berghe,et al.  Reactivation of pituitary hormone release and metabolic improvement by infusion of growth hormone-releasing peptide and thyrotropin-releasing hormone in patients with protracted critical illness. , 1999, The Journal of clinical endocrinology and metabolism.

[24]  D. Dunger,et al.  Recombinant human insulin-like growth factor-I abolishes changes in insulin requirements consequent upon growth hormone pulsatility in young adults with type I diabetes mellitus. , 1998, Metabolism: clinical and experimental.

[25]  R. Wolfe,et al.  The effect of prolonged euglycemic hyperinsulinemia on lean body mass after severe burn. , 2002, Surgery.

[26]  T. Tani,et al.  Treatment of septic shock with a protease inhibitor in a canine model: A prospective, randomized, controlled trial , 1993, Critical care medicine.

[27]  N. McLetchie Alloxan diabetes: The sorcerer and his apprentice , 1982, Diabetologia.

[28]  K. Asadullah,et al.  Monocyte deactivation in septic patients: Restoration by IFN-γ treatment , 1997, Nature Medicine.

[29]  E. Schleicher,et al.  Elevated glucose levels stimulate transforming growth factor-beta 1 (TGF-beta 1), suppress interleukin IL-2, IL-6 and IL-10 production and DNA synthesis in peripheral blood mononuclear cells. , 1996, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[30]  M Schetz,et al.  Intensive insulin therapy in critically ill patients. , 2001, The New England journal of medicine.

[31]  P. Barie,et al.  Low lipid concentrations in critical illness: implications for preventing and treating endotoxemia. , 1996, Critical care medicine.

[32]  G. Grunkemeier,et al.  Glucose control lowers the risk of wound infection in diabetics after open heart operations. , 1997, The Annals of thoracic surgery.

[33]  C. Stehouwer,et al.  The influence of improved glycaemic control with insulin and sulphonylureas on acute phase and endothelial markers in Type II Diabetic subjects , 2000, Diabetologia.

[34]  Insulin infusion improves neutrophil function in diabetic cardiac surgery patients. , 1999 .

[35]  B. Wajchenberg,et al.  Effect of glycemic control on growth hormone and IGFBP-1 secretion in patients with type I diabetes mellitus , 1996, Journal of endocrinological investigation.

[36]  R. Levy,et al.  Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. , 1972, Clinical chemistry.

[37]  H. Baumann,et al.  Insulin is a prominent modulator of the cytokine-stimulated expression of acute-phase plasma protein genes. , 1992, Molecular and cellular biology.

[38]  G. Gaulton,et al.  Assessment of the diabetogenic drugs alloxan and streptozotocin as models for the study of immune defects in diabetic mice , 1985, Diabetologia.

[39]  D. Chinkes,et al.  Stimulation of Muscle Protein Synthesis by Long‐Term Insulin Infusion in Severely Burned Patients , 1995, Annals of surgery.

[40]  L. Gavin,et al.  Glucose and insulin reverse the effects of fasting on 3,5,3'-triiodothyronine neogenesis in primary cultures of rat hepatocytes. , 1987, Endocrinology.

[41]  B A Mizock,et al.  Alterations in carbohydrate metabolism during stress: a review of the literature. , 1995, The American journal of medicine.

[42]  W. Fraser,et al.  Neutrophil Bactericidal Function in Diabetes Mellitus: Evidence for Association with Blood Glucose Control , 1995, Diabetic medicine : a journal of the British Diabetic Association.

[43]  G. Dhonneur,et al.  Impairment of polymorphonuclear neutrophil functions precedes nosocomial infections in critically ill patients , 2002, Critical care medicine.

[44]  D. Chinkes,et al.  A submaximal dose of insulin promotes net skeletal muscle protein synthesis in patients with severe burns. , 1999, Annals of surgery.

[45]  H. Sheehan,et al.  NECROSIS OF ISLETS OF LANGERHANS PRODUCED EXPERIMENTALLY , 1943 .

[46]  U. Das Is insulin an antiinflammatory molecule? , 2001, Nutrition.

[47]  A. Beddoe,et al.  Aggressive nutritional support does not prevent protein loss despite fat gain in septic intensive care patients. , 1987, The Journal of trauma.