Minerva Foundation Institute for Medical Research, Helsinki, Finland.
Department of Medicine, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.
Diabetes Care. 2018 Aug;41(8):1732-1739. doi: 10.2337/dc18-0071. Epub 2018 May 29.
Nonalcoholic fatty liver disease (i.e., increased intrahepatic triglyceride [IHTG] content), predisposes to type 2 diabetes and cardiovascular disease. Adipose tissue lipolysis and hepatic de novo lipogenesis (DNL) are the main pathways contributing to IHTG. We hypothesized that dietary macronutrient composition influences the pathways, mediators, and magnitude of weight gain-induced changes in IHTG.
We overfed 38 overweight subjects (age 48 ± 2 years, BMI 31 ± 1 kg/m, liver fat 4.7 ± 0.9%) 1,000 extra kcal/day of saturated (SAT) or unsaturated (UNSAT) fat or simple sugars (CARB) for 3 weeks. We measured IHTG (H-MRS), pathways contributing to IHTG (lipolysis ([H]glycerol) and DNL (HO) basally and during euglycemic hyperinsulinemia), insulin resistance, endotoxemia, plasma ceramides, and adipose tissue gene expression at 0 and 3 weeks.
Overfeeding SAT increased IHTG more (+55%) than UNSAT (+15%, < 0.05). CARB increased IHTG (+33%) by stimulating DNL (+98%). SAT significantly increased while UNSAT decreased lipolysis. SAT induced insulin resistance and endotoxemia and significantly increased multiple plasma ceramides. The diets had distinct effects on adipose tissue gene expression.
Macronutrient composition of excess energy influences pathways of IHTG: CARB increases DNL, while SAT increases and UNSAT decreases lipolysis. SAT induced the greatest increase in IHTG, insulin resistance, and harmful ceramides. Decreased intakes of SAT could be beneficial in reducing IHTG and the associated risk of diabetes.
非酒精性脂肪性肝病(即肝内甘油三酯含量增加)可导致 2 型糖尿病和心血管疾病。脂肪组织脂肪分解和肝脏从头合成(DNL)是导致肝内甘油三酯增加的主要途径。我们假设,饮食中的宏量营养素组成会影响这些途径、介导物以及体重增加引起肝内甘油三酯变化的程度。
我们让 38 名超重受试者(年龄 48 ± 2 岁,BMI 31 ± 1 kg/m,肝脂肪 4.7 ± 0.9%)每天额外摄入 1000 大卡的饱和(SAT)或不饱和(UNSAT)脂肪或简单糖(CARB),持续 3 周。我们在 0 周和 3 周时测量了肝内甘油三酯(H-MRS)、肝内甘油三酯增加的主要途径(脂肪分解[H]甘油)和在正常血糖高胰岛素血症期间的 DNL(HO)、胰岛素抵抗、内毒素血症、血浆神经酰胺和脂肪组织基因表达。
SAT 过量喂养使肝内甘油三酯增加了 55%,而 UNSAT 仅增加了 15%(< 0.05)。CARB 通过刺激 DNL 增加了 33%。SAT 显著增加,而 UNSAT 减少脂肪分解。SAT 诱导了胰岛素抵抗和内毒素血症,并显著增加了多种血浆神经酰胺。这些饮食对脂肪组织基因表达有明显不同的影响。
过量能量的宏量营养素组成影响肝内甘油三酯的途径:CARB 增加 DNL,而 SAT 增加和 UNSAT 减少脂肪分解。SAT 引起的肝内甘油三酯、胰岛素抵抗和有害神经酰胺增加最多。减少 SAT 的摄入量可能有助于减少肝内甘油三酯和相关的糖尿病风险。