Study2012Industry funded

Funded in part by GlaxoSmithKline

Brown adipose tissue oxidative metabolism contributes to energy expenditure during acute cold exposure in humans

Ouellet V, Labbé SM, Blondin DP, Phoenix S, Guérin B, Haman F, Turcotte EE, Richard D, Carpentier AC

The Journal of clinical investigation · 793 citations

Review labels

Industry funded

Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.

How it was studied

Design
Controlled clinical trial (classified by our AI screen)
Studied in
People
Main outcome
Health markers and function

Who paid for it

Funding
Industry funded
Company
GlaxoSmithKline
Nonprofit
Canadian Diabetes Association
University or hospital
Université Laval
University or hospital
Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval
Government
Canadian Institutes of Health Research
Grants
Canadian Diabetes Association (OG‐3‐10‐2970‐AC)

Based on 5 listed funder(s).

Publication

Published
2012-01-24 · J Clin Invest · vol. 122 · issue 2 · pp. 545–552
Publisher
American Society for Clinical Investigation
Cited
997 citations · more than 100% of similar papers · 47.1× the field average
Impact
Top 10% most cited in its field
References
40 works
Access
Open access (repository copy)
Research areas
Adipose Tissue and Metabolism · Exercise and Physiological Responses · Thermoregulation and physiological responses
Keywords
Brown adipose tissue, Thermogenesis, NEFA, Endocrinology, Internal medicine, Oxidative phosphorylation, Adipose tissue, Thermogenin, Biology, Carbohydrate metabolism, Metabolism, Chemistry, Biochemistry, Medicine, Insulin
MeSH
animals, humans, fluorodeoxyglucose f18, blood glucose, fatty acids, nonesterified, positron-emission tomography, body temperature, energy metabolism, body temperature regulation, thermogenesis, adult, male, adipose tissue, brown, cold temperature, young adult

9 authors

From CA

  • V. OuelletInstitut universitaire de cardiologie et de pneumologie de Québec
  • Sébastien M. LabbéUniversité de Sherbrooke
  • Denis P. BlondinMontfort Hospital
  • Serge PhoenixUniversité de Sherbrooke
  • Brigitte GuérinUniversité de Sherbrooke
  • François HamanMontfort Hospital

Abstract

Brown adipose tissue (BAT) is vital for proper thermogenesis during cold exposure in rodents, but until recently its presence in adult humans and its contribution to human metabolism were thought to be minimal or insignificant. Recent studies using PET with 18F-fluorodeoxyglucose (18FDG) have shown the presence of BAT in adult humans. However, whether BAT contributes to cold-induced nonshivering thermogenesis in humans has not been proven. Using PET with 11C-acetate, 18FDG, and 18F-fluoro-thiaheptadecanoic acid (18FTHA), a fatty acid tracer, we have quantified BAT oxidative metabolism and glucose and nonesterified fatty acid (NEFA) turnover in 6 healthy men under controlled cold exposure conditions. All subjects displayed substantial NEFA and glucose uptake upon cold exposure. Furthermore, we demonstrated cold-induced activation of oxidative metabolism in BAT, but not in adjoining skeletal muscles and subcutaneous adipose tissue. This activation was associated with an increase in total energy expenditure. We found an inverse relationship between BAT activity and shivering. We also observed an increase in BAT radio density upon cold exposure, indicating reduced BAT triglyceride content. In sum, our study provides evidence that BAT acts as a nonshivering thermogenesis effector in humans.

Abstract via Europe PMC. Copyright remains with the authors or publisher.

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