Increased rate of whole body lipolysis before and after 9 days of bed rest in healthy young men born with low birth weight
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Increased rate of whole body lipolysis before and after 9 days of bed rest in healthy young men born with low birth weight. / Alibegovic, Amra Ciric; Hojbjerre, Lise; Sonne, Mette; Hall, Gerrit van; Alsted, Thomas Junker; Kiens, Bente; Stallknecht, Bente; Dela, Flemming; Vaag, Allan.
In: American Journal of Physiology: Endocrinology and Metabolism, Vol. 298, No. 3, 2010, p. E555-E564.Research output: Contribution to journal › Journal article › peer-review
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T1 - Increased rate of whole body lipolysis before and after 9 days of bed rest in healthy young men born with low birth weight
AU - Alibegovic, Amra Ciric
AU - Hojbjerre, Lise
AU - Sonne, Mette
AU - Hall, Gerrit van
AU - Alsted, Thomas Junker
AU - Kiens, Bente
AU - Stallknecht, Bente
AU - Dela, Flemming
AU - Vaag, Allan
N1 - CURIS 2010 5200 011
PY - 2010
Y1 - 2010
N2 - Background: Individuals born with low birth weight (LBW) are at risk of developing type 2 diabetes mellitus (T2D), which may be precipitated by physical inactivity. Methods: 22 LBW and 23 controls were studied before and after bed rest by the hyperinsulinemic euglycemic clamp combined with indirect calorimetry, infusion of stable isotope tracers, preceded by an intravenous glucose tolerance test. Results: LBW subjects had similar BMI, but elevated abdominal obesity compared with controls. The basal rate of whole body lipolysis (WBL) was elevated in LBW subjects with and without correction for abdominal obesity before and after bed rest (all P = 0.01). Skeletal muscle hormone sensitive lipase (HSL) protein expression and phosphorylation at ser 565 were similar in the two groups. Bed rest resulted in a decrease in WBL and an increased skeletal muscle HSL Ser565 phosphorylation indicating a decreased HSL activity in both groups. All subjects developed peripheral insulin resistance in response to bed rest (all P < 0.0001) with no differences between groups. LBW subjects developed hepatic insulin resistance in response to bed rest. Conclusions: Increased WBL may contribute to the development of hepatic insulin resistance when exposed to bed rest in LBW subjects. Nine days of bed rest causes severe peripheral insulin resistance, reduced WBL and skeletal muscle HSL activity, as well as a compensatory increased insulin secretion, with no differences in LBW subjects and controls.
AB - Background: Individuals born with low birth weight (LBW) are at risk of developing type 2 diabetes mellitus (T2D), which may be precipitated by physical inactivity. Methods: 22 LBW and 23 controls were studied before and after bed rest by the hyperinsulinemic euglycemic clamp combined with indirect calorimetry, infusion of stable isotope tracers, preceded by an intravenous glucose tolerance test. Results: LBW subjects had similar BMI, but elevated abdominal obesity compared with controls. The basal rate of whole body lipolysis (WBL) was elevated in LBW subjects with and without correction for abdominal obesity before and after bed rest (all P = 0.01). Skeletal muscle hormone sensitive lipase (HSL) protein expression and phosphorylation at ser 565 were similar in the two groups. Bed rest resulted in a decrease in WBL and an increased skeletal muscle HSL Ser565 phosphorylation indicating a decreased HSL activity in both groups. All subjects developed peripheral insulin resistance in response to bed rest (all P < 0.0001) with no differences between groups. LBW subjects developed hepatic insulin resistance in response to bed rest. Conclusions: Increased WBL may contribute to the development of hepatic insulin resistance when exposed to bed rest in LBW subjects. Nine days of bed rest causes severe peripheral insulin resistance, reduced WBL and skeletal muscle HSL activity, as well as a compensatory increased insulin secretion, with no differences in LBW subjects and controls.
U2 - 10.1152/ajpendo.00223.2009
DO - 10.1152/ajpendo.00223.2009
M3 - Journal article
C2 - 19996383
VL - 298
SP - E555-E564
JO - American Journal of Physiology - Endocrinology and Metabolism
JF - American Journal of Physiology - Endocrinology and Metabolism
SN - 0193-1849
IS - 3
ER -
ID: 17111772