首页> 美国卫生研究院文献>American Journal of Physiology - Endocrinology and Metabolism >Novel Aspects of Adipocyte Biology: Activation of β3-adrenoceptors increases in vivo free fatty acid uptake and utilization in brown but not white fat depots in high-fat-fed rats
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Novel Aspects of Adipocyte Biology: Activation of β3-adrenoceptors increases in vivo free fatty acid uptake and utilization in brown but not white fat depots in high-fat-fed rats

机译:脂肪细胞生物学的新方面:β3-肾上腺素受体的激活增加了高脂饮食大鼠体内棕色而不是白色脂肪库中体内游离脂肪酸的摄取和利用

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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 β3-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 β3-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 ([14C]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, β3-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 β3-agonism in obesity.
机译:棕色脂肪组织(BAT)的激活和白色脂肪组织(WAT)的褐变为肥胖和2型糖尿病提供了潜在的新疗法。在这里,我们使用多放射性示踪技术研究了β3-肾上腺素能刺激对组织特异性摄取和储存游离脂肪酸(FFA)的影响及其对饮食诱导的肥胖大鼠体内FFA代谢的影响。 Wistar雄性大鼠高脂喂养12周,并通过以下方式给予β3-激动剂CL316,243(CL,1 mg·kg -1 ·day -1 )或盐水最近3周内的渗透性微型泵。然后将大鼠禁食并在麻醉下急性注入示踪剂混合物([ 14 C]棕榈酸酯和部分代谢的R-[ 3 H]溴棕榈酸酯)。 CL输注降低了体重增加并禁食了血浆葡萄糖水平。虽然核心体温不受影响,但红外热成像显示输注CL后尾部散热增加。有趣的是,CL明显增加了肩FA间和肾周BAT中FFA的储存和利用,而FFA向骨骼肌的通量却减少了。在此肥胖症大鼠模型中,仅在CL输注大鼠的附睾WAT储库中检测到偶发的米色脂肪细胞群,CL输注后FFA摄取或WAT的利用率没有变化。综上所述,β3激动剂使FFA通向BAT的通量强劲增加,并提高了利用率。 BAT激活的增加最有可能驱使尾部散热增加,以维持热力学。我们的结果强调了肥胖中β3受体激动剂褐色脂肪的定量作用。

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