Modulating absorption and postprandial handling of dietary fatty acids by structuring fat in the meal: a randomized crossover clinical trial

被引:93
|
作者
Vors, Cecile [1 ,2 ]
Pineau, Gaelle [4 ]
Gabert, Laure [3 ,5 ]
Drai, Jocelyne [5 ,10 ,11 ]
Louche-Pelissier, Corinne [5 ,10 ]
Defoort, Catherine [6 ,7 ,8 ]
Lairon, Denis [6 ,7 ,8 ]
Desage, Michel [3 ,5 ]
Danthine, Sabine [9 ]
Lambert-Porcheron, Stephanie [5 ]
Vidal, Hubert [4 ]
Laville, Martine [5 ]
Michalski, Marie-Caroline [1 ,2 ,5 ]
机构
[1] INRA, USC1362, Cardiovasc Metab Diabet & Nutr Lab, CarMeN, Villeurbanne, France
[2] INSA Lyon, IMBL, F-69621 Villeurbanne, France
[3] Univ Lyon, Villeurbanne, France
[4] INSERM, CarMeN, U1060, Oullins, France
[5] CRNH Rhone Alpes, Oullins, France
[6] INSERM, UMR1062, Nutr Obes & Risk Thrombosis Lab, F-13258 Marseille, France
[7] INRA, UMR1260, Marseille, France
[8] Aix Marseille Univ, Fac Med, Marseille, France
[9] Univ Liege, GxABT, Dept Food Sci & Formulat, Gembloux, Belgium
[10] Hosp Civils Lyon, Lyon, France
[11] Ctr Hosp Lyon Sud, Biochim Lab, Lyon, France
来源
关键词
TRIGLYCERIDE-RICH LIPOPROTEINS; EMULSIFIED LIPIDS; METABOLISM; EMULSIONS; DIGESTION; OBESITY; RISK; RAT; CHYLOMICRONS; OXIDATION;
D O I
10.3945/ajcn.112.043976
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Prolonged postprandial hypertriglyceridemia is a potential risk factor for cardiovascular diseases. In the context of obesity, this is associated with a chronic imbalance of lipid partitioning oriented toward storage and not toward beta-oxidation. Objective: We tested the hypothesis that the physical structure of fat in a meal can modify the absorption, chylomicron transport, and further metabolic handling of dietary fatty acids. Design: Nine normal-weight and 9 obese subjects were fed 40 g milk fat (+[C-13]triacylglycerols), either emulsified or nonemulsified, in breakfasts of identical composition. We measured the postprandial triacylglycerol content and size of the chylomicron-rich fraction, plasma kinetics of ([1)3C]fatty acids, exogenous lipid oxidation with breath-test/indirect calorimetry, and fecal excretion. Results: The emulsified fat resulted in earlier (>1 h) and sharper chylomicron and [C-13]fatty acid peaks in plasma than in spread fat in both groups (P < 0.0001). After 2 h, the emulsified fat resulted in greater apolipoprotein B-48 concentrations (9.7 +/- 0.7 compared with 7.1 +/- 0.9 mg/L; P < 0.05) in the normal-weight subjects than did the spread fat. In the obese subjects, emulsified fat resulted in a 3-fold greater chylomicron size (218 +/- 24 nm) compared with the spread fat (P < 0.05). The emulsified fat induced higher dietary fatty acid spillover in plasma and a sharper (CO2)-C-13 appearance, which provoked increased exogenous lipid oxidation in each group: from 45% to 52% in normal-weight subjects (P < 0.05) and from 40% to 57% in obese subjects (P < 0.01). Conclusion: This study supports a new concept of "slow vs fast fat," whereby intestinal absorption can be modulated by structuring dietary fat to modulate postprandial lipemia and lipid beta-oxidation in humans with different BMIs. This trial was registered at clinical-trials.gov as NCT01249378. Am J Clin Nutr 2013;97:23-36.
引用
收藏
页码:23 / 36
页数:14
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