Improved tolerance to sequential glucose loading (Staub-Traugott effect): size and mechanisms.

Improved glucose tolerance to sequential glucose loading (Staub-Traugott effect) is an important determinant of day-to-day glycemic exposure. Its mechanisms have not been clearly established. We recruited 17 healthy volunteers to receive two sequential oral glucose tolerance tests (OGTTs), at time 0 min and 180 min (Study I). The protocol was repeated on a separate day (Study II) except that plasma glucose was clamped at 8.3 mmol/l between 60 and 180 min. beta-Cell function was analyzed by mathematical modeling of C-peptide concentrations. In a subgroup, glucose kinetics were measured by a triple-tracer technique (infusion of [6,6-(2)H(2)]glucose and labeling of the 2 glucose loads with [1-(2)H]glucose and [U-(13)C]glucose). In both Studies I and II, the plasma glucose response to the second OGTT equaled 84 +/- 2% (P = 0.003) of the response to the first OGTT. Absolute insulin secretion was lower (37.8 +/- 4.3 vs. 42.8 +/- 5.1 nmol/m(2), P = 0.02), but glucose potentiation (i.e., higher secretion at the same glycemia) was stronger (1.08 +/- 0.02- vs. 0.92 +/- 0.02-fold, P = 0.006), the increment being higher in Study II (+36 +/- 5%) than Study I (+19 +/- 6%, P < 0.05). In pooled data, a higher glucose area during the first OGTT was associated with a higher potentiation during the second OGTT (rho=0.60, P = 0.002). Neither insulin clearance nor glucose clearance differed between loads, and appearance of glucose over 3 h totalled 60 +/- 6 g for the first load and 52 +/- 5 g for the second load (P = not significant). Fasting endogenous glucose production [13.3 +/- 0.6 micromol x min(-1) x kg fat-free mass (FFM)(-1)] averaged 6.0 +/- 3.8 micromol x min(-1) x kg FFM(-1) between 0 and 180 min and 1.7 +/- 2.6 between 180 and 360 min (P < 0.03). Glucose potentiation and stronger suppression of endogenous glucose release are the main mechanisms underlying the Staub-Traugott effect.

[1]  E. Ferrannini,et al.  Effect of Pioglitazone on the Metabolic and Hormonal Response to a Mixed Meal in Type II Diabetes , 2007, Clinical pharmacology and therapeutics.

[2]  Karl Traugott über das Verhalten des Blutzuckerspiegels bei Wiederholter und Verschiedener Art Enteraler Zuckerzufuhr und Dessen Bedeutung für die Leberfunktion , 1922, Klinische Wochenschrift.

[3]  Andrea Mari,et al.  A circulatory model for calculating non-steady-state glucose fluxes. Validation and comparison with compartmental models , 2003, Comput. Methods Programs Biomed..

[4]  Andrea Mari,et al.  Meal and oral glucose tests for assessment of beta -cell function: modeling analysis in normal subjects. , 2002, American journal of physiology. Endocrinology and metabolism.

[5]  Andrea Mari,et al.  A Model-Based Method for Assessing Insulin Sensitivity From the Oral Glucose Tolerance Test , 2001 .

[6]  J. Holst,et al.  Degradation of endogenous and exogenous gastric inhibitory polypeptide in healthy and in type 2 diabetic subjects as revealed using a new assay for the intact peptide. , 2000, The Journal of clinical endocrinology and metabolism.

[7]  A Mari,et al.  Dose-response characteristics of insulin action on glucose metabolism: a non-steady-state approach. , 2000, American journal of physiology. Endocrinology and metabolism.

[8]  S A Jebb,et al.  Evaluation of the novel Tanita body-fat analyser to measure body composition by comparison with a four-compartment model. , 2000, The British journal of nutrition.

[9]  F. Nuttall,et al.  Effect of Added Fat on the Plasma Glucose and Insulin Response to Ingested Potato Given in Various Combinations as Two Meals in Normal Individuals , 1994, Diabetes Care.

[10]  Dunbar Jm,et al.  Premixed insulin preparations in pen syringes maintain glycemic control and are preferred by patients. , 1994 .

[11]  J. Holst,et al.  Tissue and Plasma Concentrations of Amidated and Glycine-Extended Glucagon-Like Peptide I in Humans , 1994, Diabetes.

[12]  J. Holst,et al.  Effect of glucagon-like peptide-1 (proglucagon 78-107amide) on hepatic glucose production in healthy man. , 1994, Metabolism: clinical and experimental.

[13]  K. Polonsky,et al.  Prior feeding Alters the Response to the 50-g Glucose Challenge Test in Pregnancy: The Staub-Traugott Effect revisited , 1993, Diabetes Care.

[14]  Jeppe Sturis,et al.  Estimation of Insulin Secretion Rates from C-Peptide Levels: Comparison of Individual and Standard Kinetic Parameters for C-Peptide Clearance , 1992, Diabetes.

[15]  B. Mitchell,et al.  Does fasting interval affect the glucose challenge test? , 1990, American journal of obstetrics and gynecology.

[16]  R. Brunken,et al.  Potentiation of glucose-stimulated insulin release by tolazamide and paradoxical absence of glucose facilitation (Staub effect) in non-insulin-dependent diabetes. , 1986, Metabolism: clinical and experimental.

[17]  R. Moxley,et al.  Enhancement of insulin action after oral glucose ingestion. , 1986, The Journal of clinical investigation.

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

[19]  E. Cerasi,et al.  The Staub-Traugott effect. Evidence for multifactorial regulation of a physiological function. , 1982, Scandinavian journal of clinical and laboratory investigation.

[20]  A. Lawrence,et al.  Preservation of glucose tolerance and insulin secretory response to repeated glucose loads by the feeding of minimal glucose during prolonged fasting , 1981 .

[21]  E. Cerasi Potentiation of insulin release by glucose in man. , 1975, Acta endocrinologica.

[22]  M. Goldstein,et al.  Acute glucose loads in insulinized pancreatectomized dogs. , 1973, The Journal of laboratory and clinical medicine.

[23]  J. Roussy,et al.  Study of the factors regulating the disposal of repeated glucose injections. , 1971, Metabolism: clinical and experimental.

[24]  R. Metz,et al.  Effects of repetitive glucose loads on plasma concentrations of glucose, insulin and free fatty acids: paradoxical insulin responses in subjects with mild glucose intolerance. , 1970, The Journal of clinical endocrinology and metabolism.

[25]  A. J. Szabo,et al.  Improved Glucose Disappearance Following Repeated Glucose Administration: Serum Insulin, Growth Hormone and Free Fatty Acid Levels During the Staub-Traugott Effect , 1969, Diabetes.

[26]  D. Streeten,et al.  MEASUREMENT OF GLUCOSE DISPOSAL RATES IN NORMAL AND DIABETIC HUMAN SUBJECTS AFTER REPEATED INTRAVENOUS INJECTIONS OF GLUCOSE. , 1964, The Journal of clinical endocrinology and metabolism.

[27]  O. Somersalo Staub effect in children; studies of the blood sugar regulation by means of double and triple glucose tolerance tests. , 1950, Acta paediatrica. Supplementum.

[28]  S. Soskin Role of the Endocrines in the Regulation of Blood Sugar1 , 1944 .

[29]  G. L. Foster STUDIES ON CARBOHYDRATE METABOLISM II. AN INTERPRETATION OF THE BLOOD SUGAR PHENOMENA FOLLOWING THE INGESTION OF GLUCOSE , 1923 .

[30]  W. Smith,et al.  Studies on Carbohydrate Metabolism: On the Formation of an Anti-Diabetic Hormone by the Action of a Bacillus. (Preliminary Communication.). , 1923, The Biochemical journal.

[31]  I. Hirschman,et al.  STUDIES ON BLOOD SUGAR , 1917 .