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果糖和蔗糖饮料而非葡萄糖饮料会促进肝脏从头合成脂肪:一项随机对照试验。

Fructose- and sucrose- but not glucose-sweetened beverages promote hepatic de novo lipogenesis: A randomized controlled trial.

机构信息

Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ) and University of Zurich (UZH), Switzerland.

Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ) and University of Zurich (UZH), Switzerland; Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital and University of Bern, Switzerland.

出版信息

J Hepatol. 2021 Jul;75(1):46-54. doi: 10.1016/j.jhep.2021.02.027. Epub 2021 Mar 6.

Abstract

BACKGROUND & AIMS: Excessive fructose intake is associated with increased de novo lipogenesis, blood triglycerides, and hepatic insulin resistance. We aimed to determine whether fructose elicits specific effects on lipid metabolism independently of excessive caloric intake.

METHODS

A total of 94 healthy men were studied in this double-blind, randomized trial. They were assigned to daily consumption of sugar-sweetened beverages (SSBs) containing moderate amounts of fructose, sucrose (fructose-glucose disaccharide) or glucose (80 g/day) in addition to their usual diet or SSB abstinence (control group) for 7 weeks. De novo fatty acid (FA) and triglyceride synthesis, lipolysis and plasma free FA (FFA) oxidation were assessed by tracer methodology.

RESULTS

Daily intake of beverages sweetened with free fructose and fructose combined with glucose (sucrose) led to a 2-fold increase in basal hepatic fractional secretion rates (FSR) compared to control (median FSR %/day: sucrose 20.8 (p = 0.0015); fructose 19.7 (p = 0.013); control 9.1). Conversely, the same amounts of glucose did not change FSR (median of FSR %/day 11.0 (n.s.)). Fructose intake did not change basal secretion of newly synthesized VLDL-triglyceride, nor did it alter rates of peripheral lipolysis, nor total FA and plasma FFA oxidation. Total energy intake was similar across groups.

CONCLUSIONS

Regular consumption of both fructose- and sucrose-sweetened beverages in moderate doses - associated with stable caloric intake - increases hepatic FA synthesis even in a basal state; this effect is not observed after glucose consumption. These findings provide evidence of an adaptative response to regular fructose exposure in the liver.

LAY SUMMARY

This study investigated the metabolic effects of daily sugar-sweetened beverage consumption for several weeks in healthy lean men. It revealed that beverages sweetened with the sugars fructose and sucrose (glucose and fructose combined), but not glucose, increase the ability of the liver to produce lipids. This change may pave the way for further unfavorable effects on metabolic health.

CLINICAL TRIAL REGISTRATION NUMBER

NCT01733563.

摘要

背景与目的

过量摄入果糖会导致从头合成脂肪增加、血液甘油三酯增加和肝胰岛素抵抗。本研究旨在确定果糖是否会在不增加热量摄入的情况下对脂质代谢产生特定影响。

方法

本双盲、随机试验共纳入 94 名健康男性。他们被分配到每天饮用添加适量果糖、蔗糖(果糖-葡萄糖二糖)或葡萄糖(80g/天)的含糖饮料(SSB)组,同时饮用 SSB 或不饮用 SSB(对照组),持续 7 周。通过示踪剂法评估从头脂肪酸(FA)和甘油三酯合成、脂肪分解和血浆游离 FA(FFA)氧化。

结果

与对照组相比,单独摄入游离果糖或果糖与葡萄糖(蔗糖)混合摄入,每日饮料摄入可使基础肝脂肪酸分泌率(FSR)增加 2 倍(中位 FSR%/天:蔗糖 20.8(p=0.0015);果糖 19.7(p=0.013);对照组 9.1)。相反,相同量的葡萄糖不会改变 FSR(中位 FSR%/天 11.0(n.s.))。果糖摄入不会改变新合成的 VLDL-甘油三酯的基础分泌,也不会改变外周脂肪分解率,或总 FA 和血浆 FFA 氧化率。各组的总能量摄入相似。

结论

在稳定热量摄入的情况下,经常摄入适量的果糖和蔗糖甜味饮料,即使在基础状态下,也会增加肝脏 FA 的合成;而葡萄糖的摄入则没有这种效果。这些发现为肝脏对果糖的适应性反应提供了证据。

概要

本研究调查了在健康瘦人中,数周内每天饮用含糖饮料对代谢的影响。结果表明,用果糖和蔗糖(葡萄糖和果糖的混合物)而不是葡萄糖调味的饮料会增加肝脏产生脂质的能力。这种变化可能为代谢健康的进一步不利影响铺平道路。

临床试验注册号

NCT01733563。

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