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United States Department of Agriculture, Agricultural Research Service, Children's Nutrition Research Center, and Endocrinology and Metabolism Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030
We recently demonstrated in
neonatal pigs that, with amino acids and glucose maintained at fasting
levels, the stimulation of protein synthesis in longissimus dorsi
muscle with feeding can be reproduced by a physiological rise in
insulin alone. In the current report, we determine whether the response
of protein synthesis to insulin in the neonatal pig is 1)
present in muscles of different fiber types, 2) proportional
in myofibrillar and sarcoplasmic proteins, 3) associated
with increased translational efficiency and ribosome number, and
4) present in other peripheral tissues and in viscera.
Hyperinsulinemic-euglycemic-amino acid clamps were performed in 7- and
26-day-old pigs infused with 0, 30, 100, or 1,000 ng · kg
0.66 · min
1 of
insulin to reproduce insulin levels present in fasted, fed, refed, and
supraphysiological conditions, respectively. Tissue protein
synthesis was measured using a flooding dose of
L-[4-3H]phenylalanine. Insulin increased
protein synthesis in gastrocnemius muscle and, to a lesser degree,
masseter muscle. The degree of stimulation of protein synthesis by
insulin was similar in myofibrillar and sarcoplasmic proteins. Insulin
increased translational efficiency but had no effect on ribosome number
in muscle. All of these insulin-induced changes in muscle protein
synthesis decreased with age. Insulin also stimulated protein synthesis
in cardiac muscle and skin but not in liver, intestine, spleen,
pancreas, or kidney. The results support the hypothesis that insulin
mediates the feeding-induced stimulation of myofibrillar and
sarcoplasmic protein synthesis in muscles of different fiber types in
the neonate by increasing the efficiency of translation. However,
insulin does not appear to be involved in the feeding-induced
stimulation of protein synthesis in visceral tissues. Thus different
mechanisms regulate the growth of peripheral and visceral tissues in
the neonate.
neonate; insulin action; amino acids; protein synthesis; nutrition
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