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1 Department of Molecular Physiology and Biophysics and 2 Diabetes Research and Training Center, Vanderbilt University, Nashville, Tennessee 37232-0615
The effect of concomitant intraportal infusion
of glucose and gluconeogenic amino acids (AA) on net hepatic glucose
uptake (NHGU) and glycogen synthesis was examined in 42-h-fasted dogs. After a basal period, there was a 240-min experimental period during
which somatostatin was infused continuously into a peripheral vein and
insulin and glucagon (at 3-fold basal and basal rates, respectively)
and glucose (18.3 µmol · kg
1 · min
1)
were infused intraportally. One group (PoAA,
n = 7) received an AA mixture
intraportally at 7.6 µmol · kg
1 · min
1,
whereas the other group (NoAA, n = 6)
did not receive AA. Arterial blood glucose concentrations and hepatic
glucose loads were the same in the two groups. NHGU averaged 4.8 ± 2.0 (PoAA) and 9.4 ± 2.0 (NoAA)
µmol · kg
1 · min
1
(P < 0.05), and tracer-determined
hepatic glucose uptake was 4.6 ± 1.6 (PoAA) and 10.0 ± 1.7 (NoAA)
µmol · kg
1 · min
1
(P < 0.05). AA data for PoAA and
NoAA, respectively, were as follows: arterial blood concentrations,
1,578 ± 133 vs. 1,147 ± 86 µM
(P < 0.01); hepatic loads, 56 ± 3 vs. 32 ± 4 µmol · kg
1 · min
1
(P < 0.01); and net hepatic uptakes,
14.1 ± 1.4 vs. 5.6 ± 0.4 µmol · kg
1 · min
1
(P < 0.01). The rate of net hepatic
glycogen synthesis was 7.5 ± 1.9 (PoAA) vs. 10.7 ± 2.3 (NoAA)
µmol · kg
1 · min
1
(P = 0.1). In a net sense, intraportal
gluconeogenic amino acid delivery directed glucose carbon away from the
liver. Despite this, net hepatic carbon uptake was equivalent in the
presence and absence of amino acid infusion.
liver; hyperglycemia; liver nerves; glycogen; mixed meal
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