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高脂/低碳水化合物饮食通过长期转录环调节葡萄糖代谢。

High-fat/low-carbohydrate diets regulate glucose metabolism via a long-term transcriptional loop.

作者信息

Sparks Lauren M, Xie Hui, Koza Robert A, Mynatt Randall, Bray George A, Smith Steven R

机构信息

Department of Biological Sciences, Louisiana State University and Agricultural and Mechanical College, Baton Rouge, LA, USA.

出版信息

Metabolism. 2006 Nov;55(11):1457-63. doi: 10.1016/j.metabol.2006.07.003.

Abstract

Insulin sensitivity is characterized by insulin-stimulated glucose metabolism in skeletal muscle. We hypothesized that carbohydrate metabolism and storage might be under transcriptional control. To test this hypothesis, we fed insulin-sensitive males (glucose disposal rate, 14.7 +/- 4.1 mg/kg fat-free mass [FFM] per minute) an isoenergetic high-fat/low-carbohydrate diet (HF/LCD) for 3 days with muscle biopsies before and after intervention. Oligonucleotide microarrays revealed a total of 369 genes of 18861 genes on the arrays were differentially regulated in response to diet (Bonferonni adjusted P < .01). A similar experiment was conducted in mice with a 3-week intervention using a control group and an HF/LCD group to offset the lack of a control group within the human cohort. As part of an analysis of results previously published from this data set, 7 genes in the carbohydrate metabolism pathway changed in response to the HF/LCD, and 3 genes were confirmed by quantitative reverse transcriptase-polymerase chain reaction: fructose-2,6-biphosphatase 3 (PFKFB3), pyruvate dehydrogenase kinase, isoenzyme 4 (PDK4), and glycogen synthase 1 (muscle). In a separate experiment, we fed C57Bl/6J mice an HF/LCD for 3 weeks and found that the same glucose metabolism genes were changed by approximately 70% on average. Fructose-2,6-biphosphatase 3 and pyruvate dehydrogenase kinase, isoenzyme 4 increased and glycogen synthase 1 (muscle) decreased. Combined, these results suggest a mechanism whereby HF/LCD regulates the genes necessary for glucose utilization and storage vis-á-vis transcriptional control.

摘要

胰岛素敏感性以骨骼肌中胰岛素刺激的葡萄糖代谢为特征。我们假设碳水化合物代谢和储存可能受转录控制。为验证这一假设,我们让胰岛素敏感的男性(葡萄糖处置率为每分钟14.7±4.1mg/kg去脂体重[FFM])食用等能量的高脂肪/低碳水化合物饮食(HF/LCD)3天,并在干预前后进行肌肉活检。寡核苷酸微阵列显示,阵列上18861个基因中共有369个基因因饮食而受到差异调节(经Bonferonni校正,P<0.01)。在小鼠中进行了类似实验,采用对照组和HF/LCD组进行3周干预,以弥补人类队列中缺乏对照组的不足。作为对该数据集先前发表结果分析的一部分,碳水化合物代谢途径中的7个基因因HF/LCD而发生变化,其中3个基因通过定量逆转录聚合酶链反应得到确认:果糖-2,6-双磷酸酶3(PFKFB3)、丙酮酸脱氢酶激酶同工酶4(PDK4)和糖原合酶1(肌肉)。在另一项实验中,我们让C57Bl/6J小鼠食用HF/LCD 3周,发现相同的葡萄糖代谢基因平均变化约70%。果糖-2,6-双磷酸酶3和丙酮酸脱氢酶激酶同工酶4增加,糖原合酶1(肌肉)减少。综合这些结果表明,HF/LCD通过转录控制调节葡萄糖利用和储存所需基因的一种机制。

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