Department of Food Science, The Pennsylvania State University, University Park, PA, USA.
Mol Nutr Food Res. 2014 May;58(5):1156-9. doi: 10.1002/mnfr.201300621. Epub 2013 Dec 27.
Obesity and metabolic syndrome are growing public health problems. We investigated the effects of decaffeinated green tea extract (GTE) and voluntary running exercise (Ex) alone or in combination against obesity and metabolic syndrome in high fat (HF) fed C57BL/6J mice. After 16 wk, GTE + Ex treatment reduced final body mass (27.1% decrease) and total visceral fat mass (36.6% decrease) compared to HF-fed mice. GTE + Ex reduced fasting blood glucose (17% decrease), plasma insulin (65% decrease), and insulin resistance (65% decrease) compared to HF-fed mice. GTE or Ex alone had less significant effects. In the skeletal muscle, the combination of Ex and GTE increased the expression of peroxisome proliferator-activated receptor-γ coactivator-1α (Ppargc1a), mitochondrial NADH dehydrogenase 5 (mt-Nd5), mitochondrial cytochrome b (mt-Cytb), and mitochondrial cytochrome c oxidase III (mt-Co3). An increase in hepatic expression of peroxisome proliferator-activated receptor-α (Ppara) and liver carnitine palmitoyl transferase-1α (Cpt1a) and a decrease in hepatic expression of stearoyl-CoA desaturase 1 (Scd1) mRNA was observed in GTE + Ex mice. GTE + Ex was more effective than either treatment alone in reducing diet-induced obesity. These effects are due in part to modulation of genes related to energy metabolism and de novo lipogenesis.
肥胖和代谢综合征是日益严重的公共健康问题。我们研究了脱咖啡因绿茶提取物(GTE)和自愿跑步运动(Ex)单独或联合应用对高脂肪(HF)喂养 C57BL/6J 小鼠肥胖和代谢综合征的影响。16 周后,与 HF 喂养的小鼠相比,GTE + Ex 治疗组的最终体重(降低 27.1%)和总内脏脂肪质量(降低 36.6%)降低。与 HF 喂养的小鼠相比,GTE + Ex 还降低了空腹血糖(降低 17%)、血浆胰岛素(降低 65%)和胰岛素抵抗(降低 65%)。GTE 或 Ex 单独使用的效果则不那么显著。在骨骼肌中,Ex 和 GTE 的组合增加了过氧化物酶体增殖物激活受体-γ 共激活因子-1α(Ppargc1a)、线粒体 NADH 脱氢酶 5(mt-Nd5)、线粒体细胞色素 b(mt-Cytb)和线粒体细胞色素 c 氧化酶 III(mt-Co3)的表达。与 HF 喂养的小鼠相比,GTE + Ex 组的肝脏过氧化物酶体增殖物激活受体-α(Ppara)和肝脏肉碱棕榈酰转移酶-1α(Cpt1a)的表达增加,而肝脏硬脂酰辅酶 A 去饱和酶 1(Scd1)mRNA 的表达减少。与单独使用任何一种药物相比,GTE + Ex 能更有效地减轻饮食诱导的肥胖。这些作用部分归因于与能量代谢和从头脂肪生成相关的基因的调节。