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Inhibition of Intracellular Triglyceride Lipolysis Suppresses Cold-Induced Brown Adipose Tissue Metabolism and Increases Shivering in Humans
- Source :
- Cell Metabolism. 25:438-447
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Indirect evidence from human studies suggests that brown adipose tissue (BAT) thermogenesis is fueled predominantly by fatty acids hydrolyzed from intracellular triglycerides (TGs). However, no direct experimental evidence to support this assumption currently exists in humans. The aim of this study was to determine the role of intracellular TG in BAT thermogenesis, in cold-exposed men. Using positron emission tomography with 11C-acetate and 18F-fluorodeoxyglucose, we showed that oral nicotinic acid (NiAc) administration, an inhibitor of intracellular TG lipolysis, suppressed the cold-induced increase in BAT oxidative metabolism and glucose uptake, despite no difference in BAT blood flow. There was a commensurate increase in shivering intensity and shift toward a greater reliance on glycolytic muscle fibers without modifying total heat production. Together, these findings show that intracellular TG lipolysis is critical for BAT thermogenesis and provides experimental evidence for a reciprocal role of BAT thermogenesis and shivering in cold-induced thermogenesis in humans.
- Subjects :
- Adult
Male
0301 basic medicine
medicine.medical_specialty
animal structures
Physiology
Lipolysis
Glucose uptake
Intracellular Space
Acetates
Biology
Niacin
03 medical and health sciences
chemistry.chemical_compound
Adipose Tissue, Brown
Internal medicine
Brown adipose tissue
medicine
Humans
Glycolysis
Carbon Radioisotopes
Molecular Biology
Triglycerides
Triglyceride
Shivering
Cell Biology
Cold Temperature
Kinetics
Glucose
030104 developmental biology
Endocrinology
medicine.anatomical_structure
chemistry
Organ Specificity
Regional Blood Flow
medicine.symptom
Oxidation-Reduction
Thermogenesis
Intracellular
Subjects
Details
- ISSN :
- 15504131
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Cell Metabolism
- Accession number :
- edsair.doi.dedup.....908552d54578c24f9de0e503533538c3