Insulin-induced translocation of facilitative glucose transporters in fetal/neonatal rat skeletal muscle
1 University of Pittsburgh School of Medicine, Magee-Womens Research Institute, Pittsburgh, Pennsylvania 15213-3180; and 2 Divisions of Neonatology and Developmental Biology, Department of Pediatrics, David Geffen School of Medicine at University of California-Los Angeles, Los Angeles, California...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2003-04, Vol.284 (4), p.1138-R1146 |
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Zusammenfassung: | 1 University of Pittsburgh School of Medicine,
Magee-Womens Research Institute, Pittsburgh, Pennsylvania
15213-3180; and 2 Divisions of Neonatology and
Developmental Biology, Department of Pediatrics, David Geffen
School of Medicine at University of California-Los Angeles, Los
Angeles, California 90095-1752
We examined
the effect of insulin on fetal/neonatal rat skeletal muscle GLUT-1 and
GLUT-4 concentrations and subcellular distribution by employing
immunohistochemical analysis and subcellular fractionation followed by
Western blot analysis. We observed that insulin did not alter total
GLUT-1 or GLUT-4 concentrations or the GLUT-1 subcellular distribution
in fetal/neonatal or adult skeletal muscle in 60 min. The basal and
insulin-induced changes in subcellular distribution of GLUT-4 were
different between the fetal/neonatal and adult skeletal muscle. Under
basal conditions, sarcolemma-associated GLUT-4 was higher in the
newborn compared with the adult, translating into a higher glucose
transport. In contrast, insulin-induced translocation of GLUT-4 to the
sarcolemma- and insulin-induced glucose transport was lower in the
newborn compared with the adult. This age-related change results in
enhanced basal glucose transport to fuel myocytic proliferation and
differentiation while relatively curbing the insulin-dependent glucose
transport in the newborn.
development; glucose transport; subcellular localization
*
J. He and M. Thamotharan contributed equally to this work. |
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ISSN: | 0363-6119 1522-1490 |
DOI: | 10.1152/ajpregu.00560.2002 |