Aberrant insulin-induced GLUT4 translocation predicts glucose intolerance in the offspring of a diabetic mother
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Thamotharan, M
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USA
Thamotharan, M
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McKnight, RA
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USA
McKnight, RA
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Thamotharan, S
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USA
Thamotharan, S
[1
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Kao, DJ
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USA
Kao, DJ
[1
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Devaskar, SU
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USA
Devaskar, SU
[1
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[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Div Neonatol & Dev Biol, Los Angeles, CA 90095 USA
We examined the long-term effect of in utero exposure to streptozotocin-induced maternal diabetes on the progeny that postnatally received either ad libitum access to milk by being fed by control mothers (CM/DP) or were subjected to relative nutrient restriction by being fed by diabetic mothers (DM/DP) compared with the control progeny fed by control mothers (CM/CP). There was increased food intake, glucose intolerance, and obesity in the CM/DP group and diminished food intake, glucose tolerance, and postnatal growth restriction in the DM/DP group, persisting in the adult. These changes were associated with aberrations in hormonal and metabolic profiles and alterations in hypothalamic neuropeptide Y concentrations. By use of subfractionation and Western blot analysis techniques, the CM/DP group demonstrated a higher skeletal muscle sarcolemma-associated ( days 1 and 60) and white adipose tissue plasma membrane-associated (day 60) GLUT4 in the basal state with a lack of insulin-induced translocation. The DM/DP group demonstrated a partial amelioration of this change observed in the CM/DP group. We conclude that the offspring of a diabetic mother with ad libitum postnatal nutrition demonstrates increased food intake and resistance to insulin-induced translocation of GLUT4 in skeletal muscle and white adipose tissue. This in turn leads to glucose intolerance and obesity at a later stage ( day 180). Postnatal nutrient restriction results in reversal of this adult phenotype, thereby explaining the phenotypic heterogeneity that exists in this population.
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Tufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USATufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USA
Du, Keyong
Murakami, Shoko
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Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USATufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USA
Murakami, Shoko
Sun, Yingmin
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Tufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USATufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USA
Sun, Yingmin
Kilpatrick, Casey L.
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Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Penn State Univ, Dept Biol, University Pk, PA 16802 USA
Penn State Univ, Ctr Mol Invest Neurol Disorders, University Pk, PA 16802 USATufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USA
Kilpatrick, Casey L.
Luscher, Bernhard
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Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Penn State Univ, Dept Biol, University Pk, PA 16802 USA
Penn State Univ, Ctr Mol Invest Neurol Disorders, University Pk, PA 16802 USATufts Med Ctr, Mol Oncol Res Inst, 800 Washington St, Boston, MA 02111 USA