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Departments of Medicine, Surgery and Radiology, State University of New York at Stony Brook, Stony Brook, New York 11794
Eighteen healthy subjects had arterialized hand and renal veins
catheterized after an overnight fast. Systemic and renal glucose and
glycerol kinetics were measured with
[6,6-2H2]glucose
and [2-13C]glycerol
before and after 180-min peripheral infusions of insulin at 0.125 (LO)
or 0.25 (HI)
mU · kg
1 · min
1
with variable
[6,6-2H2]dextrose
or saline (control). Renal plasma flow was determined by plasma
p-aminohippurate clearance. Arterial
insulin increased from 37 ± 8 to 53 ± 5 (LO) and to 102 ± 10 pM (HI, P < 0.01) but not in
control (35 ± 8 pM). Arterial glucose did not change and averaged
5.2 ± 0.1 (control), 4.7 ± 0.2 (LO), and 5.1 ± 0.2 (HI) µmol/ml; renal vein glucose decreased from 4.8 ± 0.2 to 4.5 ± 0.2 µmol/ml (LO) and from 5.3 ± 0.2 to 4.9 ± 0.1 µmol/ml
(HI) with insulin but not saline infusion (5.3 ± 0.1 µmol/ml).
Endogenous glucose production decreased from 9.9 ± 0.7 to 6.9 ± 0.5 (LO) and to 5.7 ± 0.5 (HI)
µmol · kg
1 · min
1;
renal glucose production decreased from 2.5 ± 0.6 to 1.5 ± 0.5 (LO) and to 1.2 ± 0.6 (HI)
µmol · kg
1 · min
1,
whereas renal glucose utilization increased from 1.5 ± 0.6 to 2.6 ± 0.7 (LO) and to 2.9 ± 0.7 (HI)
µmol · kg
1 · min
1
after insulin infusion (all P < 0.05 vs. baseline). Neither endogenous glucose production (10.0 ± 0.4),
renal glucose production (1.1 ± 0.4), nor renal glucose utilization
(0.8 ± 0.4) changed in the control group. During insulin infusion,
systemic gluconeogenesis from glycerol decreased from 0.67 ± 0.05 to 0.18 ± 0.02 (LO) and from 0.60 ± 0.04 to 0.20 ± 0.02 (HI)
µmol · kg
1 · min
1
(P < 0.01), and renal
gluconeogenesis from glycerol decreased from 0.10 ± 0.02 to 0.02 ± 0.02 (LO) and from 0.15 ± 0.03 to 0.09 ± 0.03 (HI)
µmol · kg
1 · min
1
(P < 0.05). In contrast, during
saline infusion, systemic (0.66 ± 0.03 vs. 0.82 ± 0.05 µmol · kg
1 · min
1)
and renal gluconeogenesis from glycerol (0.11 ± 0.02 vs. 0.41 ± 0.04 µmol · kg
1 · min
1)
increased (P < 0.05 vs. baseline).
We conclude that glucose production and utilization by the kidney are
important insulin-responsive components of glucose metabolism in humans.
kidney; carbohydrate; fuel homeostasis; turnover; glycerol kinetics
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