Abnormal renal and hepatic glucose metabolism in type 2 diabetes mellitus.

Release of glucose by liver and kidney are both increased in diabetic animals. Although the overall release of glucose into the circulation is increased in humans with diabetes, excessive release of glucose by either their liver or kidney has not as yet been demonstrated. The present experiments were therefore undertaken to assess the relative contributions of hepatic and renal glucose release to the excessive glucose release found in type 2 diabetes. Using a combination of isotopic and balance techniques to determine total systemic glucose release and renal glucose release in postabsorptive type 2 diabetic subjects and age-weight-matched nondiabetic volunteers, their hepatic glucose release was then calculated as the difference between total systemic glucose release and renal glucose release. Renal glucose release was increased nearly 300% in diabetic subjects (321+/-36 vs. 125+/-15 micromol/min, P < 0.001). Hepatic glucose release was increased approximately 30% (P = 0.03), but increments in hepatic and renal glucose release were comparable (2.60+/-0.70 vs. 2.21+/-0.32, micromol.kg-1.min-1, respectively, P = 0.26). Renal glucose uptake was markedly increased in diabetic subjects (353+/-48 vs. 103+/-10 micromol/min, P < 0.001), resulting in net renal glucose uptake in the diabetic subjects (92+/-50 micromol/ min) versus a net output in the nondiabetic subjects (21+/-14 micromol/min, P = 0.043). Renal glucose uptake was inversely correlated with renal FFA uptake (r = -0.51, P < 0.01), which was reduced by approximately 60% in diabetic subjects (10. 9+/-2.7 vs. 27.0+/-3.3 micromol/min, P < 0.002). We conclude that in type 2 diabetes, both liver and kidney contribute to glucose overproduction and that renal glucose uptake is markedly increased. The latter may suppress renal FFA uptake via a glucose-fatty acid cycle and explain the accumulation of glycogen commonly found in the diabetic kidney.

[1]  C Meyer,et al.  Human kidney free fatty acid and glucose uptake: evidence for a renal glucose-fatty acid cycle. , 1997, The American journal of physiology.

[2]  D. Leroith,et al.  Changes in Facilitative Glucose Transporter Messenger Ribonucleic Acid Levels in the Diabetic Rat Kidney. , 1997, Endocrinology.

[3]  G. Mithieux,et al.  Glucose-6-Phosphatase mRNA and Activity Are Increased to the Same Extent in Kidney and Liver of Diabetic Rats , 1996, Diabetes.

[4]  M. Stumvoll,et al.  Uptake and release of glucose by the human kidney. Postabsorptive rates and responses to epinephrine. , 1995, The Journal of clinical investigation.

[5]  S. Freytag,et al.  Overexpression of glucose transporters in rat mesangial cells cultured in a normal glucose milieu mimics the diabetic phenotype. , 1995, The Journal of clinical investigation.

[6]  M. Stumvoll,et al.  A primer on tracer methods for the study of glucose metabolism in man , 1995 .

[7]  J. Simoneau,et al.  Impaired free fatty acid utilization by skeletal muscle in non-insulin-dependent diabetes mellitus. , 1994, The Journal of clinical investigation.

[8]  R. Judd,et al.  Insulin regulation of renal glucose metabolism in conscious dogs. , 1994, The Journal of clinical investigation.

[9]  J. Dominguez,et al.  Molecular adaptations of GLUT1 and GLUT2 in renal proximal tubules of diabetic rats. , 1994, The American journal of physiology.

[10]  D. Matthews Radioactive and Stable Isotope Tracers in Biomedicine: Principles and Practice of Kinetic Analysis , 1993 .

[11]  T. Danne,et al.  Effect of High Glucose on Type IV Collagen Production by Cultured Glomerular Epithelial, Endothelial, and Mesangial Cells , 1993, Diabetes.

[12]  M. Brownlee,et al.  Glycation Products and the Pathogenesis of Diabetic Complications , 1992, Diabetes Care.

[13]  E. Toth,et al.  'Spontaneous'/uremic hypoglycemia is not a distinct entity: substantiation from a literature review. , 1991, Nephron.

[14]  A. Consoli,et al.  Mechanism of increased gluconeogenesis in noninsulin-dependent diabetes mellitus. Role of alterations in systemic, hepatic, and muscle lactate and alanine metabolism. , 1990, The Journal of clinical investigation.

[15]  F. DeRubertis,et al.  Protein kinase C is activated in glomeruli from streptozotocin diabetic rats. Possible mediation by glucose. , 1989, The Journal of clinical investigation.

[16]  放射線影響研究所 Technical report series , 1989 .

[17]  W. Guder,et al.  Renal substrate metabolism. , 1986, Physiological reviews.

[18]  R. DeFronzo,et al.  Effects of insulin on peripheral and splanchnic glucose metabolism in noninsulin-dependent (type II) diabetes mellitus. , 1985, The Journal of clinical investigation.

[19]  M. Steffes,et al.  Structural-functional relationships in diabetic nephropathy. , 1984, The Journal of clinical investigation.

[20]  W. Guder,et al.  Enzyme distribution along the nephron. , 1984, Kidney international.

[21]  P. Fournel,et al.  Renal enzymes during experimental diabetes mellitus in the rat. Role of insulin, carbohydrate metabolism, and ketoacidosis. , 1984, Canadian journal of physiology and pharmacology.

[22]  R. Prior,et al.  In vitro rates of oxidation and gluconeogenesis from L(+)- and D(-)lactate in bovine tissues. , 1984, Comparative biochemistry and physiology. B, Comparative biochemistry.

[23]  R. DeFronzo,et al.  Regulation of Splanchnic and Peripheral Glucose Uptake by Insulin and Hyperglycemia in Man , 1983, Diabetes.

[24]  J. Amico,et al.  Diabetic Management in Patients with Renal Failure , 1981, Diabetes Care.

[25]  R. Rizza,et al.  Effects of Acute Insulin Deficiency on Glucose and Ketone Body Turnover in Man: Evidence for the Primacy of Overproduction of Glucose and Ketone Bodies in the Genesis of Diabetic Ketoacidosis , 1980, Diabetes.

[26]  N. Baquer,et al.  Glucose overutilization in diabetes: evidence from studies on the changes in hexokinase, the pentose phosphate pathway and glucuronate-xylulose pathway in rat kidney cortex in diabetes. , 1979, Biochemical and biophysical research communications.

[27]  P. Felig,et al.  Influence of Maturity-onset Diabetes on Splanchnic Glucose Balance After Oral Glucose Ingestion , 1978, Diabetes.

[28]  P. Felig,et al.  Renal Substrate Exchange in Human Diabetes Mellitus , 1975, Diabetes.

[29]  R. Pitts,et al.  CO2 production from plasma free fatty acids by the intact functioning kidney of the dog. , 1974, The American journal of physiology.

[30]  A. Tucker,et al.  Effects of insulin on gluconeogenesis and cyclic AMP levels in perfused livers from diabetic rats. , 1973, Biochimica et biophysica acta.

[31]  R. Dzúrik,et al.  Relation between the uptake of glucose and fatty acids by the rat kidney in vivo. , 1972, Physiologia Bohemoslovaca.

[32]  A. Svanborg,et al.  Arterio-hepatic venous differences of free fatty acids and amino acids. Studies in patients with diabetes or essential hypercholesterolemia, and in healthy individuals. , 2009, Acta medica Scandinavica.

[33]  N. Stamm,et al.  Regulation of gluconeogenesis and glycolysis: studies of mechanisms controlling enzyme activity. , 1967, Advances in enzyme regulation.

[34]  R. Kreisberg,et al.  Mechanism for the stimulation of gluconeogenesis by fatty acids in perfused rat liver. , 1966, Proceedings of the National Academy of Sciences of the United States of America.

[35]  M. West,et al.  Ultrastructural observations on renal glycogen in normal and pathologic human kidneys. , 1966, Laboratory investigation; a journal of technical methods and pathology.

[36]  H. Krebs,et al.  ACCELERATION OF RENAL GLUCONEOGENESIS BY KETONE BODIES AND FATTY ACIDS. , 1965, The Biochemical journal.

[37]  G. Cahill,et al.  Metabolism of C14-labeled substrates by rabbit kidney cortex and medulla. , 1962, The American journal of physiology.

[38]  V. Dole,et al.  An Abnormality of Nonesterified Fatty Acid Metabolism in Diabetes Mellitus , 1957, Diabetes.

[39]  C. Teng,et al.  Studies on carbohydrate metabolism in rat liver slices. II. The effect of fasting and of hormonal deficiencies. , 1953, The Journal of biological chemistry.

[40]  B. Billing,et al.  Hepatic glucose output and hepatic insulin sensitivity in diabetes mellitus. , 1951, Lancet.

[41]  C. Brun A rapid method for the determination of para-aminohippuric acid in kidney function tests. , 1951, The Journal of laboratory and clinical medicine.