
With the recent rediscovery of brown fat in adult humans, our outlook on adipose tissue biology has undergone a paradigm shift. While we attempt to identify, recruit, and activate classic brown fat stores in humans, identification of beige fat has also raised the possibility of browning our white fat stores. Whether such transformation of human white fat depots can be achieved to enhance the whole body oxidative potential remains to be seen. Evidence to date, however, largely points toward a major oxidative role only for classic brown fat depots, at least in rodents. White fat stores seem to provide the main fuel for sustaining thermogenesis via lipolysis. Interestingly, molecular markers consistent with both classic brown and beige fat identity can be observed in human supraclavicular depot, thereby complicating the discussion on beige fat in humans. Here, we review the recent advances made in our understanding of brown and beige fat in humans and mice. We further provide an overview of their plausible physiological relevance to whole body energy metabolism.
sympathetic nervous system, FATTY-ACID OXIDATION, ENERGY-EXPENDITURE, brown fat, thermogenesis, ADULT HUMANS, NERVOUS-SYSTEM OUTFLOW, NONSHIVERING THERMOGENESIS, DIET-INDUCED THERMOGENESIS, UNCOUPLING PROTEIN-1 GENE, beige fat, GLUCOSE-HOMEOSTASIS, WHITE FAT, CENTRAL SENSORY CIRCUITS
sympathetic nervous system, FATTY-ACID OXIDATION, ENERGY-EXPENDITURE, brown fat, thermogenesis, ADULT HUMANS, NERVOUS-SYSTEM OUTFLOW, NONSHIVERING THERMOGENESIS, DIET-INDUCED THERMOGENESIS, UNCOUPLING PROTEIN-1 GENE, beige fat, GLUCOSE-HOMEOSTASIS, WHITE FAT, CENTRAL SENSORY CIRCUITS
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