Human kidney free fatty acid and glucose uptake: evidence for a renal glucose-fatty acid cycle.

To determine the relationship between free fatty acids (FFA) and glucose uptake by the human kidney, 12 postabsorptive normal volunteers underwent renal vein catheterization and were infused to isotopic steady state with [6-3H]glucose and [9,10-3H]palmitate. Arterial and renal vein palmitate specific activities were not significantly different (3,533 +/- 219 vs. 3,549 +/- 220 dpm/mumol, P = 0.64). Palmitate renal fractional extraction and uptake determined isotopically (7.2 +/- 1.1% and 9.1 +/- 1.4 mumol/min) were not significantly different from those calculated by net balance measurements (8.3 +/- 1.2% and 9.7 +/- 1.2 mumol/min, P > 0.07 and P > 0.7, respectively). Renal palmitate uptake accounted for 8.7 +/- 1.3% of its systemic turnover. Renal linoleate and oleate fractional extraction calculated by net balance measurements (8.0 +/- 0.9 and 7.7 +/- 1.2%, respectively) were not significantly different from each other and that of palmitate (all P > 0.7). Renal uptake of palmitate, linoleate (7.9 +/- 1.0 mumol/min), and oleate (10.9 +/- 2.0 mumol/min) were all directly proportional to their arterial concentrations (r = 0.70, 0.68, and 0.63, respectively, all P < 0.025). Renal glucose uptake (93 +/- 10 mumol/min) accounted for 12.6 +/- 1.5% of its systemic turnover and was inversely related to the sum of palmitate, linoleate, and oleate uptake (r = -0.74, P < 0.01). These data indicate that in postabsorptive humans: 1) the kidney is an important site of FFA and glucose disposal, 2) a renal glucose-fatty acid cycle may exist, and 3) there appears to be little or no release into the circulation of stored renal FFA.

[1]  G. Boden Role of Fatty Acids in the Pathogenesis of Insulin Resistance and NIDDM , 1997, Diabetes.

[2]  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.

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

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

[5]  R. DeFronzo The Triumvirate: β-Cell, Muscle, Liver: A Collusion Responsible for NIDDM , 1988, Diabetes.

[6]  G Sonnenberg,et al.  Skeletal muscle glycolysis, oxidation, and storage of an oral glucose load. , 1988, The Journal of clinical investigation.

[7]  A. Consoli,et al.  Quantification of the glycolytic origin of plasma glycerol: implications for the use of the rate of appearance of plasma glycerol as an index of lipolysis in vivo. , 1988, Metabolism: clinical and experimental.

[8]  M. Jensen,et al.  Lipolysis during fasting. Decreased suppression by insulin and increased stimulation by epinephrine. , 1987, The Journal of clinical investigation.

[9]  A. Kleinzeller,et al.  Glucose transport and metabolism in rat renal proximal tubules: multicomponent effects of insulin. , 1986, Biochimica et biophysica acta.

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

[11]  C. Bogardus,et al.  Multiple disturbances of free fatty acid metabolism in noninsulin-dependent diabetes. Effect of oral hypoglycemic therapy. , 1985, The Journal of clinical investigation.

[12]  T. Kreulen,et al.  Hepatic, gut, and renal substrate flux rates in patients with hepatic cirrhosis. , 1981, The Journal of clinical investigation.

[13]  W. Guder,et al.  Triacylglycerol metabolism in kidney cortex and outer medulla. , 1980, The International journal of biochemistry.

[14]  L. Sjöström,et al.  Carbohydrate storage in man: speculations and some quantitative considerations. , 1978, Metabolism: clinical and experimental.

[15]  W. Kirkendall,et al.  Structure of neutral glycerides and phosphoglycerides of human kidney , 1975 .

[16]  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.

[17]  J. Wahren,et al.  Uptake of individual free fatty acids by skeletal muscle and liver in man. , 1972, The Journal of clinical investigation.

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

[19]  J. Cohen,et al.  The metabolic fates of palmitate in the dog kidney in vivo. Evidence for incomplete oxidation. , 1971, Nephron.

[20]  F. Díes,et al.  Substrate uptake by the dog kidney in vivo. , 1970, The American journal of physiology.

[21]  H. Krebs,et al.  The fuel of respiration of rat kidney cortex. , 1969, The Biochemical journal.

[22]  P. Felig,et al.  Liver and kidney metabolism during prolonged starvation. , 1969, The Journal of clinical investigation.

[23]  E. Newsholme,et al.  Control of glycolysis and gluconeogenesis in rat kidney cortex slices. , 1967, The Biochemical journal.

[24]  P. Schollmeyer,et al.  Substrate-utilization of the Human Kidney , 1966, Nature.

[25]  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.

[26]  R. Dzúrik,et al.  Glucose metabolism in rat kidney: influence of insulin and adrenaline , 1963, The Journal of physiology.

[27]  R. Havel,et al.  Transport of Glycerol in Human Blood∗ , 1963, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[28]  E. Newsholme,et al.  The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. , 1963, Lancet.

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

[30]  J. Spitzer,et al.  Changes in plasma free fatty acid concentrations on passage through the dog kidney. , 1961, The American journal of physiology.

[31]  F. Chinard,et al.  Renal handling of glucose in dogs. , 1959, The American journal of physiology.

[32]  K. Zierler,et al.  The quantitatively minor role of carbohydrate in oxidative metabolism by skeletal muscle in intact man in the basal state; measurements of oxygen and glucose uptake and carbon dioxide and lactate production in the forearm. , 1956, The Journal of clinical investigation.