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高脂生酮饮食会在小鼠体内诱导出一种独特的代谢状态。

A high-fat, ketogenic diet induces a unique metabolic state in mice.

作者信息

Kennedy Adam R, Pissios Pavlos, Otu Hasan, Roberson Russell, Xue Bingzhong, Asakura Kenji, Furukawa Noburu, Marino Frank E, Liu Fen-Fen, Kahn Barbara B, Libermann Towia A, Maratos-Flier Eleftheria

机构信息

Division of Endocrinology, Departmentof Medicine, Beth Israel Deaconess Medical Center, 330 Brookline Ave., Boston, MA 02215, USA.

出版信息

Am J Physiol Endocrinol Metab. 2007 Jun;292(6):E1724-39. doi: 10.1152/ajpendo.00717.2006. Epub 2007 Feb 13.

Abstract

Ketogenic diets have been used as an approach to weight loss on the basis of the theoretical advantage of a low-carbohydrate, high-fat diet. To evaluate the physiological and metabolic effects of such diets on weight we studied mice consuming a very-low-carbohydrate, ketogenic diet (KD). This diet had profound effects on energy balance and gene expression. C57BL/6 mice animals were fed one of four diets: KD; a commonly used obesogenic high-fat, high-sucrose diet (HF); 66% caloric restriction (CR); and control chow (C). Mice on KD ate the same calories as mice on C and HF, but weight dropped and stabilized at 85% initial weight, similar to CR. This was consistent with increased energy expenditure seen in animals fed KD vs. those on C and CR. Microarray analysis of liver showed a unique pattern of gene expression in KD, with increased expression of genes in fatty acid oxidation pathways and reduction in lipid synthesis pathways. Animals made obese on HF and transitioned to KD lost all excess body weight, improved glucose tolerance, and increased energy expenditure. Analysis of key genes showed similar changes as those seen in lean animals placed directly on KD. Additionally, AMP kinase activity was increased, with a corresponding decrease in ACC activity. These data indicate that KD induces a unique metabolic state congruous with weight loss.

摘要

基于低碳水化合物、高脂肪饮食的理论优势,生酮饮食已被用作一种减肥方法。为了评估此类饮食对体重的生理和代谢影响,我们研究了食用极低碳水化合物生酮饮食(KD)的小鼠。这种饮食对能量平衡和基因表达有深远影响。给C57BL/6小鼠喂食四种饮食之一:KD;常用的致肥胖高脂肪、高蔗糖饮食(HF);66%热量限制(CR);以及对照食物(C)。食用KD的小鼠摄入的热量与食用C和HF的小鼠相同,但体重下降并稳定在初始体重的85%,与CR相似。这与喂食KD的动物相比喂食C和CR的动物能量消耗增加是一致的。肝脏的微阵列分析显示KD中有独特的基因表达模式,脂肪酸氧化途径中的基因表达增加,脂质合成途径减少。在HF上变得肥胖并转为KD的动物失去了所有多余体重,改善了葡萄糖耐量,并增加了能量消耗。关键基因分析显示出与直接采用KD的瘦动物相似的变化。此外,AMP激酶活性增加,ACC活性相应降低。这些数据表明KD诱导了一种与体重减轻相一致的独特代谢状态。

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