Activation of beta(3)-adrenoceptors increases in vivo free fatty acid uptake and utilization in brown but not white fat depots in high-fat-fed rats

作者:Warner Amy; Kjellstedt Ann; Carreras Alba; Bottcher Gerhard; Peng Xiao Rong; Seale Patrick; Oakes Nicholas; Linden Daniel*
来源:American Journal of Physiology - Endocrinology And Metabolism, 2016, 311(6): E901-E910.
DOI:10.1152/ajpendo.00204.2016

摘要

Activation of brown adipose tissue (BAT) and browning of white adipose tissue (WAT) present potential new therapies for obesity and type 2 diabetes. Here, we examined the effects of beta(3)-adrenergic stimulation on tissue-specific uptake and storage of free fatty acids (FFA) and its implications for whole body FFA metabolism in diet-induced obese rats using a multi-radiotracer technique. Male Wistar rats were high fat-fed for 12 wk and administered beta(3)-agonist CL316,243 (CL, 1 mg.kg(-1).day(-1)) or saline via osmotic minipumps during the last 3 wk. The rats were then fasted and acutely infused with a tracer mixture ([C-14] palmitate and the partially metabolized R-[3H] bromopalmitate) under anesthesia. CL infusion decreased body weight gain and fasting plasma glucose levels. While core body temperature was unaffected, infrared thermography showed an increase in tail heat dissipation following CL infusion. Interestingly, CL markedly increased both FFA storage and utilization in interscapular and perirenal BAT, whereas the flux of FFA to skeletal muscle was decreased. In this rat model of obesity, only sporadic populations of beige adipocytes were detected in the epididymal WAT depot of CL-infused rats, and there was no change in FFA uptake or utilization in WAT following CL infusion. In summary, beta(3)-agonism robustly increased FFA flux to BAT coupled with enhanced utilization. Increased BAT activation most likely drove the increased tail heat dissipation to maintain thermostasis. Our results emphasize the quantitative role of brown fat as the functional target of beta(3)-agonism in obesity.

  • 出版日期2016-12-1