Abstract

While it is now understood that the proper expansion of adipose tissue is critically important for metabolic homeostasis, it is also appreciated that adipose tissues perform far more functions than simply maintaining energy balance. Adipose tissue performs endocrine functions, secreting hormones or adipokines that affect the regulation of extra-adipose tissues, and, under certain conditions, can also be major contributors to energy expenditure and the systemic metabolic rate via the activation of thermogenesis. Adipose thermogenesis takes place in brown and beige adipocytes. While brown adipocytes have been relatively well studied, the study of beige adipocytes has only recently become an area of considerable exploration. Numerous suggestions have been made that beige adipocytes can elicit beneficial metabolic effects on body weight, insulin sensitivity, and lipid levels. However, the potential impact of beige adipocyte thermogenesis on systemic metabolism is not yet clear and an understanding of beige adipocyte development and regulation is also limited. This review will highlight our current understanding of beige adipocytes and select factors that have been reported to elicit the development and activation of thermogenesis in beige cells, with a focus on factors that may represent a link between exercise and ‘beiging’, as well as the role that thyroid hormone signaling plays in beige adipocyte regulation.

Highlights

  • Obesity and the co-morbidities of metabolic syndrome are an accelerating worldwide health crisis

  • Increasing energy expenditure via thermogenesis brings with it the obvious risk that the additional heat that accompanies an increased metabolic rate could result in hyperthermia, an acute risk not shared with strategies that decrease caloric intake

  • uncoupling protein 1 (UCP1) expression is limited to brown adipose tissue (BAT) and beige adipocytes, which reside within white adipose tissue (WAT)

Read more

Summary

Introduction

Obesity and the co-morbidities of metabolic syndrome are an accelerating worldwide health crisis. There has long been an allure in utilizing thermogenesis, the conversion of energy (such as excess caloric intake) to heat, as a weight loss strategy that functions by increasing energy expenditure. Increasing energy expenditure via thermogenesis brings with it the obvious risk that the additional heat that accompanies an increased metabolic rate could result in hyperthermia, an acute risk not shared with strategies that decrease caloric intake. This risk is borne out by the misuse of the chemical uncoupler dinitrophenol, which has been shown to be highly efficacious in producing weight loss, but has resulted in overdose deaths [2,3,4]. UCP1 expression is limited to brown adipose tissue (BAT) and beige adipocytes, which reside within white adipose tissue (WAT)

White Adipose Tissue
Brown Adipose Tissue
Beige Adipocytes
Exercise and Environmental Stimulation
Irisin
Succinate
Lactate and β-Hydroxybutyrate
The Role of the Thyroid Hormone System in Beige Fat Thermogenesis
Non-UCP1 Mediated Non-Shivering Thermogenesis
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call