Departament de Bioquímica i Biotecnologia, Universitat Rovira i Virgili, Tarragona, Spain.
J Agric Food Chem. 2011 Aug 10;59(15):8491-8. doi: 10.1021/jf201775v. Epub 2011 Jul 15.
The aim of this study was to determine the effect of chronic dietary supplementation of a grape seed proanthocyanidin extract (GSPE) at a dose of 35 mg/kg body weight on energy metabolism and mitochondrial function in the skeletal muscle of Zucker obese rats. Three groups of 10 animals each were used: lean Fa/fa lean group (LG) rats, a control fa/fa obese group (OG) of rats, and an obese supplemented fa/fa proanthocyanidins obese group (POG) of rats, which were supplemented with a dose of 35 mg GSPE/kg of body weight/day during the 68 days of experimentation. Skeletal muscle energy metabolism was evaluated by determining enzyme activities, key metabolic gene expression, and immunoblotting of oxidative phosphorylation complexes. Mitochondrial function was analyzed by high-resolution respirometry using both a glycosidic and a lipid substrate. In muscle, chronic GSPE administration decreased citrate synthase activity, the amount of oxidative phosphorylation complexes I and II, and Nrf1 gene expression, without any effects on the mitochondrial oxidative capacity. This situation was associated with lower reactive oxygen species (ROS) generation. Additionally, GSPE administration enhanced the ability to oxidize pyruvate, and it also increased the activity of enzymes involved in oxidative phosphorylation including cytochrome c oxidase. There is strong evidence to suggest that GSPE administration stimulates mitochondrial function in skeletal muscle specifically by increasing the capacity to oxidize pyruvate and contributes to reduced muscle ROS generation in obese Zucker rats.
本研究旨在确定以 35 毫克/千克体重的剂量连续摄入葡萄籽原花青素提取物(GSPE)对肥胖型 Zucker 大鼠骨骼肌能量代谢和线粒体功能的影响。使用了三组各 10 只动物:瘦 Fa/fa 瘦鼠组(LG)、Fa/fa 肥胖对照组(OG)和肥胖型补充原花青素的 Fa/fa 肥胖鼠组(POG),POG 在 68 天的实验期间每天补充 35 毫克 GSPE/千克体重。通过测定酶活性、关键代谢基因表达和氧化磷酸化复合物的免疫印迹,评估骨骼肌能量代谢。通过使用糖基和脂基底物的高分辨率呼吸测定法分析线粒体功能。在肌肉中,慢性 GSPE 给药降低了柠檬酸合酶活性、氧化磷酸化复合物 I 和 II 的量以及 Nrf1 基因表达,而对线粒体氧化能力没有任何影响。这种情况与较低的活性氧(ROS)生成有关。此外,GSPE 给药增强了氧化丙酮酸的能力,还增加了包括细胞色素 c 氧化酶在内的参与氧化磷酸化的酶的活性。有强有力的证据表明,GSPE 给药通过增加氧化丙酮酸的能力来刺激骨骼肌中的线粒体功能,并有助于减少肥胖型 Zucker 大鼠肌肉中的 ROS 生成。