scholarly journals Greater early postprandial suppression of endogenous glucose production and higher initial glucose disappearance is achieved with fast‐acting insulin aspart compared with insulin aspart

2018 ◽  
Vol 20 (7) ◽  
pp. 1615-1622 ◽  
Author(s):  
Ananda Basu ◽  
Thomas R. Pieber ◽  
Ann K. Hansen ◽  
Stefanie Sach‐Friedl ◽  
Lars Erichsen ◽  
...  
2003 ◽  
Vol 285 (2) ◽  
pp. E280-E286 ◽  
Author(s):  
Farhad Zangeneh ◽  
Rita Basu ◽  
Pankaj Shah ◽  
Puneet Arora ◽  
Michael Camilleri ◽  
...  

Portal infusion of glucose at rates approximating endogenous glucose production (EGP) causes paradoxical hypoglycemia in wild-type but not GLUT2 null mice, implying activation of a specific portal glucose sensor. To determine whether this occurs in humans, glucose containing [3-3H]glucose was infused intraduodenally at rates of 3.1 mg · kg-1 · min-1 ( n = 5), 1.55 mg · kg-1 · min-1 ( n = 9), or 0/0.1 mg · kg-1 · min-1 ( n = 9) for 7 h in healthy nondiabetic subjects. [6,6-2H2]glucose was infused intravenously to enable simultaneous measurement of EGP, glucose disappearance, and the rate of appearance of the intraduodenally infused glucose. Plasma glucose concentrations fell ( P < 0.01) from 90 ± 1 to 84 ± 2 mg/dl during the 0/0.1 mg · kg-1 · min-1 id infusions but increased ( P < 0.001) to 104 ± 5 and 107 ± 3 mg/dl, respectively, during the 1.55 and 3.1 mg · kg-1 · min-1 id infusions. In contrast, insulin increased ( P < 0.05) during the 1.55 and 3.0 mg · kg-1 · min-1 infusions, reaching a peak of 10 ± 2 and 18 ± 5 μU/ml, respectively, by 2 h. Insulin concentrations then fell back to concentrations that no longer differed by study end (7 ± 1 vs. 8 ± 1 μU/ml). This resulted in comparable suppression of EGP by study end (0.84 ± 0.2 and 0.63 ± 0.1 mg · kg-1 · min-1). Glucose disappearance was higher ( P < 0.01) during the final hour of the 3.1 than 1.55 mg · kg-1 · min-1 id infusion (4.47 ± 0.2 vs. 2.6 ± 0.1 mg · kg-1 · min-1), likely because of the slightly, but not significantly, higher glucose and insulin concentrations. We conclude that, in contrast to mice, selective portal glucose delivery at rates approximating EGP does not cause hypoglycemia in humans.


2017 ◽  
Vol 41 (5) ◽  
pp. S70
Author(s):  
Jina Hahn ◽  
Ananda Basu ◽  
Thomas R. Pieber ◽  
Ann Kathrine Hansen ◽  
Stefanie Sach-Friedl ◽  
...  

1968 ◽  
Vol 46 (3) ◽  
pp. 391-398 ◽  
Author(s):  
G. Hetenyi Jr. ◽  
G. A. Wrenshall

The intravenous infusion of glucose at rates corresponding to 17–79% of the endogenous (hepatic) rate of glucose production decreased the latter in both normal and diabetic dogs. The increase in the rate of the exogenous infusion and the decrease in the rate of endogenous production were found to be positively correlated. The correlation between the change in the rate of glucose disappearance (utilization plus excretion) and the change in the rate of the exogenous infusion was significant in normal but not in diabetic dogs. The infusion of galactose had no effect on endogenous glucose production. Infusions into the cephalic vein or into the carotid artery were equally effective in decreasing endogenous glucose production. It appears that the rate of endogenous (hepatic) glucose production adapts to an exogenous glucose infusion in both normal and diabetic dogs. Such an adaptation in the rate of glucose disappearance (disposal) was observed only in normal but not in pancreatectomized dogs. Thus the role of the release of insulin in such adaptation is to increase the disposal rather than to decrease the rate of the endogenous production of glucose. The specificity of the adaptive mechanism is demonstrated by the ineffectiveness of galactose in altering glucose turnover.


Diabetes ◽  
2019 ◽  
Vol 68 (Supplement 1) ◽  
pp. 155-LB
Author(s):  
CAROLINA SOLIS-HERRERA ◽  
MARIAM ALATRACH ◽  
CHRISTINA AGYIN ◽  
HENRI HONKA ◽  
RUPAL PATEL ◽  
...  

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 1832-P
Author(s):  
ANNA SANTORO ◽  
PENG ZHOU ◽  
YAN ZHU ◽  
ODILE D. PERONI ◽  
ANDREW T. NELSON ◽  
...  

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 1037-P
Author(s):  
WENDY LANE ◽  
MAGNUS EKELUND ◽  
ÓLÖF THÓRISDÓTTIR ◽  
ESTEBAN JÓDAR ◽  
ALEJANDRA OVIEDO ◽  
...  

Diabetes ◽  
2019 ◽  
Vol 68 (Supplement 1) ◽  
pp. 246-OR
Author(s):  
MARIAM ALATRACH ◽  
CHRISTINA AGYIN ◽  
NITCHAKARN LAICHUTHAI ◽  
JOHN M. ADAMS ◽  
MUHAMMAD ABDUL-GHANI ◽  
...  

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 1898-P
Author(s):  
ADELINA I.L. LANE ◽  
SAVANNA N. WENINGER ◽  
FRANK DUCA

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