Glucosamine induces insulin resistance in vivo by affecting GLUT 4 translocation in skeletal muscle. Implications for glucose toxicity.

Glucosamine (Glmn), a product of glucose metabolism via the hexosamine pathway, causes insulin resistance in isolated adipocytes by impairing insulin-induced GLUT 4 glucose transporter translocation to the plasma membrane. We hypothesized that Glmn causes insulin resistance in vivo by a similar mechanism in skeletal muscle. We performed euglycemic hyperinsulinemic clamps (12 mU/kg/min + 3H-3-glucose) in awake male Sprague-Dawley rats with and without Glmn infusion at rates ranging from 0.1 to 6.5 mg/kg/min. After 4h of euglycemic clamping, hindquarter muscles were quick-frozen and homogenized, and membranes were subfractionated by differential centrifugation and separated on a discontinuous sucrose gradient (25, 30, and 35% sucrose). Membrane proteins were solubilized and immunoblotted for GLUT 4. With Glmn, glucose uptake (GU) was maximally reduced by 33 +/- 1%, P < 0.001. The apparent Glmn dose to reduce maximal GU by 50% was 0.1 mg/kg/min or 1/70th the rate of GU on a molar basis. Control galactosamine and mannosamine infusions had no effect on GU. Relative to baseline, insulin caused a 2.6-fold increase in GLUT 4 in the 25% membrane fraction (f), P < 0.01, and a 40% reduction in the 35%f, P < 0.05, but had no effect on GLUT 4 in the 30% f, P= NS. Addition of Glmn to insulin caused a 41% reduction of GLUT 4 in the 25%f, P < 0.05, a 29% fall in the 30%f, and prevented the reduction of GLUT 4 in the 35% f. The 30%f membranes were subjected to a second separation with a 27 and 30% sucrose gradient. Insulin mobilized GLUT 4 away from the 30%f, P < 0.05, but not the 27% f. In contrast, Glmn reduced GLUT 4 in the 27%f, P < 0.05, but not the 30%f. Thus Glmn appears to alter translocation of an insulin-insensitive GLUT 4 pool. Coinfusion of Glmn did not alter enrichment of the sarcolemmal markers 5'-nucleotidase, Na+/K+ATPase, and phospholemman in either 25, 30, or 35% f. Thus Glmn completely blocked movement of Glut 4 induced by insulin. Glmn is a potent inducer of insulin resistance in vivo by causing (at least in part) a defect intrinsic to GLUT 4 translocation and/or trafficking. These data support a potential role for Glmn to cause glucose-induced insulin resistance (glucose toxicity).

[1]  D. James,et al.  Molecular cloning and characterization of an insulin-regulatable glucose transporter , 1989, Nature.

[2]  A. Klip,et al.  Insulin‐induced translocation of glucose transporters in rat hindlimb muscles , 1987, FEBS letters.

[3]  M. Armoni,et al.  Reversal of Insulin Resistance in Diabetic Rat Adipocytes by Insulin Therapy: Restoration of Pool of Glucose Transporters and Enhancement of Glucose-Transport Activity , 1987, Diabetes.

[4]  S. Marshall,et al.  Role of amino acids in modulating glucose-induced desensitization of the glucose transport system. , 1989, The Journal of biological chemistry.

[5]  J. Avruch,et al.  Preparation and properties of plasma membrane and endoplasmic reticulum fragments from isolated rat fat cells. , 1971, Biochimica et biophysica acta.

[6]  B. Forbush Assay of Na,K-ATPase in plasma membrane preparations: increasing the permeability of membrane vesicles using sodium dodecyl sulfate buffered with bovine serum albumin. , 1983, Analytical biochemistry.

[7]  W. Garvey,et al.  Biological Actions of Insulin Are Differentially Regulated by Glucose and Insulin in Primary Cultured Adipocytes: Chronic Ability to Increase Glycogen Synthase Activity , 1994, Diabetes.

[8]  M. Laakso,et al.  Reduced capacity and affinity of skeletal muscle for insulin-mediated glucose uptake in noninsulin-dependent diabetic subjects. Effects of insulin therapy. , 1991, The Journal of clinical investigation.

[9]  H. Yki-Järvinen,et al.  Hyperglycemia Decreases Glucose Uptake in Type I Diabetes , 1987, Diabetes.

[10]  J. Olefsky,et al.  Glucose and insulin co-regulate the glucose transport system in primary cultured adipocytes. A new mechanism of insulin resistance. , 1987, The Journal of biological chemistry.

[11]  S Marshall,et al.  Coordinated regulation of glutamine:fructose-6-phosphate amidotransferase activity by insulin, glucose, and glutamine. Role of hexosamine biosynthesis in enzyme regulation. , 1991, The Journal of biological chemistry.

[12]  S. Marshall,et al.  Insulin regulation of pyruvate kinase activity in isolated adipocytes. Crucial role of glucose and the hexosamine biosynthesis pathway in the expression of insulin action. , 1992, The Journal of biological chemistry.

[13]  G. Reaven,et al.  Effect of Sulfonylurea Treatment on In Vivo Insulin Secretion and Action in Patients With Non-insulin-dependent Diabetes Mellitus , 1982, Diabetes.

[14]  S. Marshall,et al.  Complete inhibition of glucose-induced desensitization of the glucose transport system by inhibitors of mRNA synthesis. Evidence for rapid turnover of glutamine:fructose-6-phosphate amidotransferase. , 1991, The Journal of biological chemistry.

[15]  R. DeFronzo,et al.  Pathogenesis of NIDDM: A Balanced Overview , 1992, Diabetes Care.

[16]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[17]  J. A. Scarlett,et al.  Lack of in vivo insulin resistance in controlled insulin-dependent, type I, diabetic patients. , 1984, The Journal of clinical endocrinology and metabolism.

[18]  M. Birnbaum,et al.  Cellular insulin action and insulin resistance. , 1993, Baillière's Clinical Endocrinology and Metabolism.

[19]  W. Nelson Linkage of Plasma Membrane Proteins with the Membrane Skeleton: Insights into Functions in Polarized Epithelial Cells , 1993 .

[20]  J. A. Scarlett,et al.  Insulin treatment reverses the postreceptor defect in adipocyte 3-O-methylglucose transport in type II diabetes mellitus. , 1983, The Journal of clinical endocrinology and metabolism.

[21]  W. Garvey,et al.  New insights into the metabolic regulation of insulin action and insulin resistance: role of glucose and amino acids , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[22]  R. DeFronzo,et al.  Normalization of blood glucose in diabetic rats with phlorizin treatment reverses insulin-resistant glucose transport in adipose cells without restoring glucose transporter gene expression. , 1991, The Journal of clinical investigation.

[23]  E. Horton,et al.  Identification of an intracellular pool of glucose transporters from basal and insulin-stimulated rat skeletal muscle. , 1990, The Journal of biological chemistry.

[24]  H. Ginsberg,et al.  Effect of Insulin Therapy on Insulin Resistance in Type II Diabetic Subjects: Evidence for Heterogeneity , 1981, Diabetes.

[25]  G. Hart,et al.  The subcellular distribution of terminal N-acetylglucosamine moieties. Localization of a novel protein-saccharide linkage, O-linked GlcNAc. , 1986, The Journal of biological chemistry.

[26]  R. Barnard,et al.  Mechanism of insulin action on glucose transport in rat skeletal muscle. , 1988, The American journal of physiology.

[27]  W. Garvey,et al.  Glucose and insulin regulate insulin sensitivity in primary cultured adipocytes without affecting insulin receptor kinase activity. , 1991, Endocrinology.

[28]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[29]  R. Hamman,et al.  The Effect of Insulin Treatment on Insulin Secretion and Insulin Action in Type II Diabetes Mellitus , 1985, Diabetes.

[30]  R. Tjian,et al.  O-glycosylation of eukaryotic transcription factors: Implications for mechanisms of transcriptional regulation , 1988, Cell.

[31]  S. Marshall,et al.  Discovery of a metabolic pathway mediating glucose-induced desensitization of the glucose transport system. Role of hexosamine biosynthesis in the induction of insulin resistance. , 1991, The Journal of biological chemistry.

[32]  M. Birnbaum,et al.  Expression of a glucose transporter gene cloned from brain in cellular models of insulin resistance: dexamethasone decreases transporter mRNA in primary cultured adipocytes. , 1989, Molecular endocrinology.

[33]  A. Klip,et al.  Recruitment of GLUT-4 glucose transporters by insulin in diabetic rat skeletal muscle. , 1990, Biochemical and biophysical research communications.

[34]  S. Walaas,et al.  Phosphorylation of multiple sites in a 15,000 dalton proteolipid from rat skeletal muscle sarcolemma, catalyzed by adenosine 3',5'-monophosphate-dependent and calcium/phospholipid-dependent protein kinases. , 1988, Biochimica et biophysica acta.

[35]  J. Friedman,et al.  Restoration of insulin responsiveness in skeletal muscle of morbidly obese patients after weight loss. Effect on muscle glucose transport and glucose transporter GLUT4. , 1992, The Journal of clinical investigation.

[36]  R. DeFronzo,et al.  Glucose Toxicity , 1990, Diabetes Care.

[37]  R. DeFronzo,et al.  Correction of hyperglycemia with phlorizin normalizes tissue sensitivity to insulin in diabetic rats. , 1987, The Journal of clinical investigation.

[38]  J. Olefsky,et al.  Effects of Weight Loss on Mechanisms of Hyperglycemia in Obese Non-Insulin-Dependent Diabetes Mellitus , 1986, Diabetes.

[39]  C. Cobelli,et al.  In vivo glucose metabolism in the awake rat: tracer and insulin clamp studies. , 1987, Metabolism: clinical and experimental.

[40]  L. Jones,et al.  Purification and complete sequence determination of the major plasma membrane substrate for cAMP-dependent protein kinase and protein kinase C in myocardium. , 1991, The Journal of biological chemistry.

[41]  B. Hansen,et al.  Glucose-induced insulin resistance of skeletal-muscle glucose transport and uptake. , 1988, The Biochemical journal.

[42]  J. A. Scarlett,et al.  The Acute and Chronic Effects of Sulfonylurea Therapy in Type II Diabetic Subjects , 1984, Diabetes.