Treating hyperglycemia improves skeletal muscle protein metabolism in cancer patients after major surgery

Objective:Cancer and surgical stress interact to aggravate insulin resistance, protein catabolism, and glutamine depletion in skeletal muscle. We compared the effects of insulin-mediated euglycemia and moderate hyperglycemia on kinetics of protein and selected amino acids in skeletal muscle of female cancer patients after major surgery. Design:In each patient, a 24-hr period of insulin-mediated tight euglycemia (mean blood glucose, 5.8 ± 0.4 mmol/L) preceded or followed a 24-hr control period of moderate hyperglycemia (mean blood glucose, 9.6 ± 0.6 mmol/L) on the first and second day after surgery, in randomized order, according to a crossover experimental design. Setting:Intensive care unit, cancer hospital. Patients:Cancer patients after abdominal radical surgery combined with intraoperative radiation therapy. Interventions:Intensive (57 ± 11 units/24 hrs) and conventional (25 ± 5 units/24 hrs) insulin treatment during total parenteral nutrition. Measurements and Main Results:Muscle metabolism was assessed at the end of each 24-hr period of euglycemia and of hyperglycemia by leg arteriovenous catheterization with stable isotopic tracers. We found that euglycemia as compared with hyperglycemia was associated with higher (p < .05) fractional glucose uptake (16% ± 4% vs. 9% ± 3%); higher (p < .05) muscle protein synthesis and neutral net protein balance (−3 ± 3 vs. −11 ± 3 nmol phenylalanine·100 mL−1·min−1, respectively); lower (−52% ± 12%, p < .01) muscle nonprotein leucine disposal (an index of leucine oxidation) and higher (p < .05) plasma leucine concentrations; and higher (3.6 ± 1.7 times, p < .01) net de novo muscle glutamine synthesis and plasma glutamine concentrations (p < .05). Euglycemia was associated with higher (23% ± 7%, p < .05) plasma concentrations of arginine but did not affect either arginine release from muscle or plasma concentration and muscle flux of asymmetrical dimethylarginine. Rate of muscle proteolysis correlated (p < .05) with muscle release of asymmetrical dimethylarginine. Conclusions:Treating hyperglycemia improves skeletal muscle protein and amino acid metabolism in cancer patients after major surgery.

[1]  V. Baracos Cancer-associated cachexia and underlying biological mechanisms. , 2006, Annual review of nutrition.

[2]  G. Biolo,et al.  Response of muscle protein and glutamine kinetics to branched-chain-enriched amino acids in intensive care patients after radical cancer surgery. , 2006, Nutrition.

[3]  J. Bełtowski,et al.  Asymmetric dimethylarginine (ADMA) as a target for pharmacotherapy. , 2006, Pharmacological reports : PR.

[4]  B. Gornicka,et al.  Impaired glucose metabolism in colorectal cancer , 2006, Scandinavian journal of gastroenterology.

[5]  G. Biolo,et al.  Muscle glutamine depletion in the intensive care unit. , 2005, The international journal of biochemistry & cell biology.

[6]  Ilse Vanhorebeek,et al.  Intensive insulin therapy protects the endothelium of critically ill patients. , 2005, The Journal of clinical investigation.

[7]  Hui Chen,et al.  Assessing the predictive accuracy of QUICKI as a surrogate index for insulin sensitivity using a calibration model. , 2005, Diabetes.

[8]  C. Dejong,et al.  Plasma arginine concentrations are reduced in cancer patients: evidence for arginine deficiency? , 2005, The American journal of clinical nutrition.

[9]  P. Fiorina,et al.  Determination of asymmetric and symmetric dimethylarginines in plasma of hyperhomocysteinemic subjects , 2005, Amino Acids.

[10]  C. Dejong,et al.  Sepsis: An arginine deficiency state? , 2004, Critical care medicine.

[11]  H. Woerle,et al.  Paradoxical changes of muscle glutamine release during hyperinsulinemia euglycemia and hypoglycemia in humans: further evidence for the glucose-glutamine cycle. , 2004, Metabolism: clinical and experimental.

[12]  I. Rieu,et al.  Insulin and amino acids both strongly participate to the regulation of protein metabolism , 2004, Current opinion in clinical nutrition and metabolic care.

[13]  N. Willich,et al.  Intraoperative radiation therapy (IORT) in primary locally advanced and recurrent carcinoma of the rectum at a "non-dedicated" facility. , 2003, Anticancer research.

[14]  Steven E Wolf,et al.  Hyperglycemia exacerbates muscle protein catabolism in burn-injured patients , 2002, Critical care medicine.

[15]  G. Biolo,et al.  Inverse regulation of protein turnover and amino acid transport in skeletal muscle of hypercatabolic patients. , 2002, The Journal of clinical endocrinology and metabolism.

[16]  G. V. Berghe,et al.  Intensive insulin therapy in critically ill patients. , 2001, The New England journal of medicine.

[17]  Robert A. Harris,et al.  Regulation of branched-chain amino acid catabolism: nutritional and hormonal regulation of activity and expression of the branched-chain α-keto acid dehydrogenase kinase , 2001, Current opinion in clinical nutrition and metabolic care.

[18]  M. Haymond,et al.  Role of glucose in the regulation of glutamine metabolism in health and in type 1 insulin-dependent diabetes. , 2000, American journal of physiology. Endocrinology and metabolism.

[19]  G. Biolo,et al.  Inhibition of muscle glutamine formation in hypercatabolic patients. , 2000, Clinical science.

[20]  G. Biolo,et al.  Growth hormone decreases muscle glutamine production and stimulates protein synthesis in hypercatabolic patients. , 2000, American journal of physiology. Endocrinology and metabolism.

[21]  N. Deutz,et al.  Tracer methodology in whole body and organ balance metabolic studies: plasma sampling is required. A study in post-absorptive rats using isotopically labeled arginine, phenylalanine, valine and leucine. , 2000, Clinical nutrition.

[22]  D. Gore,et al.  Deficiency in peripheral glutamine production in pediatric patients with burns. , 2000, The Journal of burn care & rehabilitation.

[23]  K. M. Popov,et al.  Mechanism responsible for inactivation of skeletal muscle pyruvate dehydrogenase complex in starvation and diabetes. , 1999, Diabetes.

[24]  C Meyer,et al.  Effects of physiological hyperinsulinemia on systemic, renal, and hepatic substrate metabolism. , 1998, The American journal of physiology.

[25]  N. Deutz,et al.  Cancer reduces the metabolic response of muscle to surgical stress in the rat. , 1998, The Journal of surgical research.

[26]  D. Chinkes,et al.  Acute dichloroacetate administration increases skeletal muscle free glutamine concentrations after burn injury. , 1998, Annals of surgery.

[27]  J. Zierath,et al.  Skeletal muscle insulin resistance after trauma: insulin signaling and glucose transport. , 1998, American journal of physiology. Endocrinology and metabolism.

[28]  G. Biolo,et al.  Physiologic hyperinsulinemia stimulates protein synthesis and enhances transport of selected amino acids in human skeletal muscle. , 1995, The Journal of clinical investigation.

[29]  J O Hill,et al.  Acute hyperglycemia enhances proteolysis in normal man. , 1993, The American journal of physiology.

[30]  H. Yki-Jărvinen,et al.  Mechanisms of Hyperglycemia-Induced Insulin Resistance in Whole Body and Skeletal Muscle of Type I Diabetic Patients , 1992, Diabetes.

[31]  I. Wool,et al.  Effect of diabetes on the concentration of amino acids in plasma and heart muscle of rats. , 1966, The Biochemical journal.

[32]  M. Rennie,et al.  Branched-chain amino acids as fuels and anabolic signals in human muscle. , 2006, The Journal of nutrition.

[33]  S. Kimball,et al.  Signaling pathways and molecular mechanisms through which branched-chain amino acids mediate translational control of protein synthesis. , 2006, The Journal of nutrition.

[34]  B. Bistrian,et al.  Intensive insulin therapy in critically ill patients. , 2002, The New England journal of medicine.

[35]  P. Carroll,et al.  The metabolic consequences of critical illness: acute effects on glutamine and protein metabolism. , 1999, American journal of physiology. Endocrinology and metabolism.

[36]  M. J. Webb,et al.  IORT for locally advanced gynecological malignancies. , 1997, Frontiers of radiation therapy and oncology.

[37]  T. Wolever,et al.  The use of the glycemic index in predicting the blood glucose response to mixed meals. , 1986, The American journal of clinical nutrition.