French William W, Dridi Sami, Shouse Stephanie A, Wu Hexirui, Hawley Aubree, Lee Sun-Ok, Gu Xuan, Baum Jamie I
Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72704, USA.
Center for Poultry Excellence, Division of Agriculture, University of Arkansas, Fayetteville, AR 72704, USA.
Nutrients. 2017 Jun 8;9(6):587. doi: 10.3390/nu9060587.
A primary factor in controlling and preventing obesity is through dietary manipulation. Diets higher in protein have been shown to improve body composition and metabolic health during weight loss. The objective of this study was to examine the effects of a high-protein diet versus a moderate-protein diet on muscle, liver and fat metabolism and glucose regulation using the obese Zucker rat. Twelve-week old, male, Zucker (fa/fa) and lean control (Fa/fa) rats were randomly assigned to either a high-protein (40% energy) or moderate-protein (20% energy) diet for 12 weeks, with a total of four groups: lean 20% protein (L20; = 8), lean 40% protein (L40; = 10), obese 20% protein (O20; = 8), and obese 40% protein (O40; = 10). At the end of 12 weeks, animals were fasted and euthanized. There was no difference in food intake between L20 and L40. O40 rats gained less weight and had lower food intake ( < 0.05) compared to O20. O40 rats had lower liver weight ( < 0.05) compared to O20. However, O40 rats had higher orexin ( < 0.05) levels compared to L20, L40 and O20. Rats in the L40 and O40 groups had less liver and muscle lipid deposition compared to L20 and L40 diet rats, respectively. O40 had decreased skeletal muscle mechanistic target of rapamycin complex 1 (mTORC1) phosphorylation and peroxisome proliferator-activated receptor gamma (PPARγ) mRNA expression compared to O20 ( < 0.05), with no difference in 5' AMP-activated protein kinase (AMPK), eukaryotic translation initiation factor 4E binding protein 1 (4EBP1), protein kinase B (Akt) or p70 ribosomal S6 kinase (p70S6K) phosphorylation. The data suggest that high-protein diets have the potential to reduce weight gain and alter metabolism, possibly through regulation of an mTORC1-dependent pathway in skeletal muscle.
控制和预防肥胖的一个主要因素是通过饮食控制。高蛋白饮食已被证明在减肥期间可改善身体成分和代谢健康。本研究的目的是使用肥胖 Zucker 大鼠,研究高蛋白饮食与中等蛋白饮食对肌肉、肝脏和脂肪代谢以及葡萄糖调节的影响。将 12 周龄的雄性 Zucker(fa/fa)大鼠和瘦对照(Fa/fa)大鼠随机分为高蛋白(40%能量)或中等蛋白(20%能量)饮食组,为期 12 周,共四个组:瘦 20%蛋白组(L20;n = 8)、瘦 40%蛋白组(L40;n = 10)、肥胖 20%蛋白组(O20;n = 8)和肥胖 40%蛋白组(O40;n = 10)。在 12 周结束时,动物禁食并安乐死。L20 和 L40 之间的食物摄入量没有差异。与 O20 相比,O40 大鼠体重增加较少且食物摄入量较低(P < 0.05)。与 O20 相比,O40 大鼠肝脏重量较低(P < 0.05)。然而,与 L20、L40 和 O20 相比,O40 大鼠的食欲素水平较高(P < 0.05)。与 L20 和 O20 饮食组的大鼠相比,L40 和 O40 组的大鼠肝脏和肌肉脂质沉积较少。与 O20 相比,O40 的骨骼肌雷帕霉素复合物 1(mTORC1)磷酸化和过氧化物酶体增殖物激活受体γ(PPARγ)mRNA 表达降低(P < 0.05),5' 腺苷酸活化蛋白激酶(AMPK)、真核翻译起始因子 4E 结合蛋白 1(4EBP1)、蛋白激酶 B(Akt)或 p70 核糖体 S6 激酶(p70S6K)磷酸化没有差异。数据表明,高蛋白饮食有可能减轻体重增加并改变代谢,可能是通过调节骨骼肌中依赖 mTORC1 的途径实现的。