首页> 外文期刊>Journal of medicinal food >Ethanolic extracts of Brassica campestris spp. rapa roots prevent high-fat diet-induced obesity via beta(3)-adrenergic regulation of white adipocyte lipolytic activity.
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Ethanolic extracts of Brassica campestris spp. rapa roots prevent high-fat diet-induced obesity via beta(3)-adrenergic regulation of white adipocyte lipolytic activity.

机译:芸苔属植物的乙醇提取物。 rapa根通过β(3)-肾上腺素调节白色脂肪细胞脂解活性来防止高脂饮食诱导的肥胖。

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The influence of ethanolic extracts of Brassica campestris spp. rapa roots (EBR) on obesity was examined in imprinting control region (ICR) mice fed a high-fat diet (HFD) and in 3T3-L1 adipocytes. The ICR mice used were divided into regular diet, HFD, EBR (50 mg/kg/day EBR administered orally), and orlistat (10 mg/kg/day orlistat administered orally) groups. The molecular mechanism of the anti-obesity effect of EBR was investigated in 3T3-L1 adipocytes as well as in HFD-fed ICR mice. In the obese mouse model, both weight gain and epididymal fat accumulation were highly suppressed by the daily oral administration of 50 mg/kg EBR for 8 weeks, whereas the overall amount of food intake was not affected. EBR treatment induced the expression in white adipocytes of lipolysis-related genes, including beta(3)-adrenergic receptor (beta(3)-AR), hormone-sensitive lipase (HSL), adipose triglyceride lipase, and uncoupling protein 2. Furthermore, the activation of cyclic AMP-dependent protein kinase, HSL, and extracellular signal-regulated kinase was induced in EBR-treated 3T3-L1 cells. The lipolytic effect of EBR involved beta(3)-AR modulation, as inferred from the inhibition by the beta(3)-AR antagonist propranolol. These results suggest that EBR may have potential as a safe and effective anti-obesity agent via the inhibition of adipocyte lipid accumulation and the stimulation of beta(3)-AR-dependent lipolysis.
机译:甘蓝型油菜乙醇提取物的影响。在饲喂高脂饮食(HFD)的印迹控制区(ICR)小鼠和3T3-L1脂肪细胞中检查了肥胖的rapa根(EBR)。使用的ICR小鼠分为常规饮食,HFD,EBR(50毫克/千克/天,口服EBR)和奥利司他(10毫克/千克/天,口服奥利司他)组。在3T3-L1脂肪细胞以及HFD喂养的ICR小鼠中研究了EBR抗肥胖作用的分子机制。在肥胖的小鼠模型中,每天口服50 mg / kg EBR连续8周可显着抑制体重增加和附睾脂肪积聚,而食物摄入总量不会受到影响。 EBR处理诱导了脂肪分解相关基因在白色脂肪细胞中的表达,这些基因包括β(3)-肾上腺素能受体(β(3)-AR),激素敏感性脂肪酶(HSL),脂肪甘油三酸酯脂肪酶和解偶联蛋白2。此外,在EBR处理的3T3-L1细胞中诱导了环状AMP依赖性蛋白激酶,HSL和细胞外信号调节激酶的激活。从BR​​(3)-AR拮抗剂普萘洛尔的抑制作用推断,EBR的脂解作用涉及β(3)-AR的调节。这些结果表明,EBR可能通过抑制脂肪细胞脂质蓄积和刺激β(3)-AR依赖性脂解而具有作为安全有效的抗肥胖药的潜力。

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