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Whole Body and Regional Quantification of Active Human Brown Adipose Tissue Using 18F-FDG PET/CT
Published on: April 1, 2019
Functional brown adipose tissue in healthy adults
Kirsi A Virtanen1, Martin E Lidell, Janne Orava
1Turku PET Center, University of Turku, Finland.
Healthy adults possess metabolically active brown adipose tissue. Positron-emission tomography (PET) revealed a 15-fold increase in cold-induced glucose uptake in specific adipose tissues, confirming brown fat presence.
Area of Science:
- Human physiology
- Metabolic research
- Adipose tissue biology
Background:
- Brown adipose tissue (BAT) is known for its role in non-shivering thermogenesis.
- Its presence and metabolic activity in adult humans have been debated.
- Understanding adult BAT can offer insights into metabolic health and energy expenditure.
Purpose of the Study:
- To investigate the presence and metabolic activity of brown adipose tissue in healthy adult humans.
- To quantify cold-induced metabolic changes in specific human adipose depots.
- To characterize the molecular and morphological markers of brown adipocytes in adults.
Main Methods:
- Positron-emission tomography (PET) scans were used to measure glucose uptake.
- Cold exposure was employed to stimulate metabolic activity.
- Biopsy specimens were analyzed for messenger RNA (mRNA) and protein expression of UCP1.
- Morphological assessment of adipose tissue was performed.
Main Results:
- Cold exposure induced a 15-fold increase in glucose uptake in paracervical and supraclavicular adipose tissue.
- Biopsies confirmed the presence of uncoupling protein 1 (UCP1) mRNA and protein.
- Morphological analysis revealed multilocular lipid droplets characteristic of brown adipocytes.
Conclusions:
- The study provides strong evidence for substantial amounts of metabolically active brown adipose tissue in healthy adult humans.
- These findings highlight the potential role of adult BAT in human energy metabolism.
- The results warrant further investigation into the physiological significance and therapeutic potential of human BAT.
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