Department of Rehabilitation Medicine of Korean Medicine, College of Korean Medicine, Dongguk University, Dongdaero 123, Gyeongju-si 38066, Korea.
Department of Rehabilitation Medicine of Korean Medicine, College of Korean Medicine, Dongguk University, Donggukro 27, Ilsandong-gu, Goyang-si 10326, Korea.
Int J Mol Sci. 2018 Jan 17;19(1):278. doi: 10.3390/ijms19010278.
Targeting energy expenditure offers a strategy for treating obesity more effectively and safely. In previous studies, we found that the root of Koidzumi (Atractylodis Rhizoma Alba, ARA) increased energy metabolism in C2C12 cells. Here, we investigated the effects of ARA on obesity and glucose intolerance by examining energy metabolism in skeletal muscle and brown fat in high-fat diet (HFD) induced obese mice. ARA decreased body weight gain, hepatic lipid levels and serum total cholesterol levels, but did not modify food intake. Fasting serum glucose, serum insulin levels and glucose intolerance were all improved in ARA treated mice. Furthermore, ARA increased peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC1α) expression, and the phosphorylation of adenosine monophosphate-activated protein kinase (AMPK) in skeletal muscle tissues, and also prevented skeletal muscle atrophy. In addition, the numbers of brown adipocytes and the expressions of PGC1α and uncoupling protein 1 (UCP1) were elevated in the brown adipose tissues of ARA treated mice. Our results show that ARA can prevent diet-induced obesity and glucose intolerance in C5BL/6 mice and suggests that the mechanism responsible is related to the promotion of energy metabolism in skeletal muscle and brown adipose tissues.
靶向能量消耗为治疗肥胖提供了一种更有效和更安全的策略。在之前的研究中,我们发现白术的根茎可以增加 C2C12 细胞的能量代谢。在这里,我们通过检查高脂肪饮食(HFD)诱导肥胖小鼠的骨骼肌和棕色脂肪中的能量代谢,研究了白术对肥胖和葡萄糖耐量的影响。白术可降低体重增加、肝脂质水平和血清总胆固醇水平,但不改变食物摄入。白术处理的小鼠空腹血清葡萄糖、血清胰岛素水平和葡萄糖耐量均得到改善。此外,白术增加了骨骼肌组织中过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC1α)的表达以及腺苷单磷酸激活蛋白激酶(AMPK)的磷酸化,并防止了骨骼肌萎缩。此外,在白术处理的小鼠的棕色脂肪组织中,棕色脂肪细胞的数量以及 PGC1α和解偶联蛋白 1(UCP1)的表达均升高。我们的结果表明,白术可以预防 C5BL/6 小鼠的饮食诱导肥胖和葡萄糖耐量异常,并且表明其机制与促进骨骼肌和棕色脂肪组织中的能量代谢有关。