Abstract. Brown adipose tissue (BAT) is the site of sympathetically activated adaptive thermognenesis during cold exposure and after hyperphagia, thereby controlling whole-body energy expenditure (EE) and body fat. Radionuclide imaging studies have demonstrated that adult humans have metabolically active BAT composed of mainly beige/brite adipocytes, recently identified brown-like adipocytes. The inverse relationship between the BAT activity and body fatness suggests that BAT is, because of its energy dissipating activity, protective against body fat accumulation in humans as it is in small rodents. In fact, either repeated cold exposure or daily ingestion of some food ingredients acting on transient receptor potential channels recruits BAT in parallel with increased EE and decreased body fat. In addition to the sympathetic nervous system, several endocrine factors are also shown to recruit BAT. Thus, BAT is a promising therapeutic target for combating human obesity and related metabolic disorders.Key words: Beige/brite adipocyte, Body fat, Brown adipose tissue, Energy expenditure, ObesityIn mAmmAls, there are two types of adipose tissue, white and brown adipose tissues, which are quite different in the physiological functions. White adipose tissue (WAT) is the site of energy storage, while brown adipose tissue (BAT) is specialized for non-shivering thermogenesis to dissipate energy as heat. In small rodents, BAT has long been recognized as the major site of sympathetically activated adaptive thermogenesis during cold exposure and probably after spontaneous overfeeding. This specific thermogenic organ has currently gathered increasing attention as a therapeutic target for combating human obesity and related metabolic disorders [1][2][3]. This is because of several remarkable advancements in BAT research over the last few years. First, being against the conventional view that human BAT is functional only in neonates, recent radionuclide imaging studies have revealed the existence of a considerable amount of BAT in adult humans [4][5][6][7]. There are now piles of evidence indicating BAT as a significant regulatory site of wholebody energy expenditure (EE) and body fatness in not only small rodents but also humans. Second, studies in rodent models revealed two types of themogenic adipocytes arising from distinct developmental lineages: "classical" brown adipocytes" and "beige/brite" adipocytes [8, 9]. Several key transcriptional regulators and signaling molecules in the developmental pathways of brown and beige/brite adipocytes have been identified [10]. Third, while the sympathetic nervous system is a central regulator of BAT function, several endocrine/ paracrine molecules were also identified as significant activators/recruiters of BAT [11]. Lastly, some studies investigating the effects of BAT transplantation suggest possible roles of BAT in the regulation of glucose and lipid metabolism through some body fat-independent mechanisms [12, 13]. Based on these findings, this review summarizes the regulatory mechan...