Fasting, But Not Exercise, Increases Adipose Triglyceride Lipase (ATGL) Protein and Reduces G(0)/G(1) Switch Gene 2 (G0S2) Protein and mRNA Content in Human Adipose Tissue
Adult
Male
0301 basic medicine
Cross-Over Studies
C-Peptide
Human Growth Hormone
Biopsy
Lipolysis
Subcutaneous Fat
Calorimetry, Indirect
Cell Cycle Proteins
Fasting
Lipase
Fatty Acids, Nonesterified
3. Good health
Young Adult
03 medical and health sciences
Glucose Clamp Technique
Humans
Insulin
RNA, Messenger
Exercise
DOI:
10.1210/jc.2011-0149
Publication Date:
2011-05-26T04:34:31Z
AUTHORS (7)
ABSTRACT
Abstract
Context:
Fasting and exercise are characterized by increased lipolysis, but the underlying mechanisms are not fully understood.
Objective:
The study was designed to test whether fasting and exercise affect mRNA and protein levels of adipose triglyceride lipase (ATGL) and G(0)/G(1) switch gene 2 (G0S2), a recently discovered ATGL inhibitor, in humans.
Design and Participants:
We studied eight healthy men (age, 25.5 ± 4.3 yr) for 6 h (a 4-h basal and a 2-h clamp period) on three occasions in a randomized crossover design: 1) in the basal state and after; 2) 72-h fasting; and 3) 1-h exercise (65% VO2max). Subcutaneous abdominal adipose tissue (AT) biopsies were taken at t = 30 and 270 min.
Setting:
The study was conducted at a university hospital research unit.
Results:
Circulating free fatty acids and GH were increased, and C-peptide was decreased by both fasting and exercise. During fasting, insulin failed to suppress free fatty acid levels, suggesting AT insulin resistance. ATGL protein was increased 44% (P < 0.001), and G0S2 mRNA and protein were decreased 56% (P = 0.02) and 54% (P = 0.01), respectively, after fasting, but both ATGL and G0S2 were unaffected by exercise. Protein levels of hormone-sensitive lipase and comparative gene identification-58 were unaffected throughout.
Conclusions:
We found increased AT content of ATGL and decreased protein and mRNA content of the ATGL inhibitor G0S2, suggesting increased ATGL activity during fasting, but not after short-term exercise. These findings are compatible with the notion that the ATGL-G0S2 complex is an important long-term regulator of lipolysis under physiological conditions such as fasting in humans.
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