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Diabetes, Vol 38, Issue 5 618-624, Copyright © 1989 by American Diabetes Association
Failure of insulin infusion to stimulate fractional muscle protein synthesis in type I diabetic patients. Anabolic effect of insulin and decreased proteolysis
PJ Pacy, KS Nair, C Ford and D Halliday
Nutrition Research Group, Clinical Research Centre, Harrow, Middlesex, United Kingdom.
We evaluated the influence of insulin on fractional mixed skeletal muscle
protein synthesis (FMPS) in eight type I (insulin-dependent) diabetic
patients in the postabsorptive state. FMPS was calculated from the
increment in [13C]leucine in mixed skeletal muscle protein obtained by
serial percutaneous needle biopsy during a continuous 8-h intravenous
infusion of L-[13C]leucine. We used the plasma [13C]-alpha-ketoisocaproate
(representing intracellular leucine labeling) as the precursor pool of
protein synthesis for our calculations. FMPS during the insulin treatment
(0.0472 +/- 0.0046%/h; plasma glucose 4.6 +/- 1.0 mM) was not different
from FMPS during insulin deprivation (0.0499 +/- 0.0046%/h; plasma glucose
16.4 +/- 0.5 mM). Using plasma [13C]-alpha-ketoisocaproate at isotopic
plateau for calculation of leucine flux and as the precursor for leucine
oxidation, we further confirmed the findings of our group and others that
insulin treatment decreases leucine flux, leucine oxidation, and the
nonoxidative portion of leucine flux. Our data on direct measurement of
FMPS provide further evidence that the anabolic effect of insulin in the
postabsorptive type I diabetic patient is mediated via reduction of
proteolysis rather than by increasing protein synthesis.

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Copyright © 1989 by the American Diabetes Association.
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