Steingoetter Andreas, Radovic Tijana, Buetikofer Simon, Curcic Jelena, Menne Dieter, Fried Michael, Schwizer Werner, Wooster Tim J
From the Division of Gastroenterology and Hepatology, University Hospital Zurich, Zurich, Switzerland (AS, TR, SB, JC, MF, and WS); the Institute for Biomedical Engineering, University and Federal Institute of Technology Zurich, Zurich, Switzerland (AS); Menne Biomed Consulting, Tübingen, Germany (DM); the Commonwealth Scientific and Industrial Research Organisation (CSIRO) Preventive Health Flagship, Werribee, Australia (TJW); and the Nestlé Research Centre, Vers Chez les Blancs, Switzerland (TJW).
Am J Clin Nutr. 2015 Apr;101(4):714-24. doi: 10.3945/ajcn.114.100263. Epub 2015 Feb 25.
Efficient fat digestion requires fat processing within the stomach and fat sensing in the intestine. Both processes also control gastric emptying and gastrointestinal secretions.
We aimed to visualize the influence of the intragastric stability of fat emulsions on their dynamics of gastric processing and structuring and to assess the effect this has on gastrointestinal motor and secretory functions.
Eighteen healthy subjects with normal body mass index (BMI) were studied on 4 separate occasions in a double-blind, randomized, crossover design. Magnetic resonance imaging (MRI) data of the gastrointestinal tract and blood triglycerides were recorded before and for 240 min after the consumption of the following 4 different fat emulsions: lipid emulsion 1 (LE1; acid stable, 0.33 μm), lipid emulsion 2 (LE2; acid stable, 52 μm), lipid emulsion 3 (LE3; acid unstable, solid fat, 0.32 μm), and lipid emulsion 4 (LE4; acid unstable, liquid fat, 0.38 μm).
Intragastric emulsion instability was associated with a change in gastric emptying. Acid-unstable emulsions exhibited biphasic and faster emptying profiles than did the 2 acid-stable emulsions (P ≤ 0.0001). When combined with solid fat (LE3), different dynamics of postprandial gallbladder volume were induced (P ≤ 0.001). For acid-stable emulsions, a reduction of droplet size by 2 orders of magnitude [LE1 (0.33 μm) compared with LE2 (52 μm)] delayed gastric emptying by 38 min. Although acid-stable (LE1 and LE2) and redispersible (LE4) emulsions caused a constant increase in blood triglycerides, no increase was detectable for LE3 (P < 0.0001). For LE3, MRI confirmed the generation of large fat particles during gastric processing, which emptied into and progressed through the small intestine.
MRI allows the detailed characterization of the in vivo fate of lipid emulsions. The acute effects of lipid emulsions on gastric emptying, gallbladder volume, and triglyceride absorption are dependent on microstructural changes undergone during consumption. Gastric peristalsis and secretion were effective at redispersing pools of liquid fat in the stomach. This trial was registered at clinicaltrials.gov as NCT01253005.
有效的脂肪消化需要在胃内进行脂肪加工以及在肠道内进行脂肪感知。这两个过程还控制着胃排空和胃肠道分泌。
我们旨在观察脂肪乳剂在胃内的稳定性对其胃加工和结构形成动态过程的影响,并评估其对胃肠运动和分泌功能的作用。
采用双盲、随机、交叉设计,在4个不同时间段对18名体重指数(BMI)正常的健康受试者进行研究。在摄入以下4种不同脂肪乳剂之前及之后240分钟记录胃肠道的磁共振成像(MRI)数据和血液甘油三酯水平:脂质乳剂1(LE1;酸稳定,0.33μm)、脂质乳剂2(LE2;酸稳定,52μm)、脂质乳剂3(LE3;酸不稳定,固体脂肪,0.32μm)和脂质乳剂4(LE4;酸不稳定,液体脂肪,0.38μm)。
胃内乳剂不稳定性与胃排空变化相关。酸不稳定的乳剂比两种酸稳定的乳剂表现出双相且更快的排空曲线(P≤0.0001)。当与固体脂肪(LE3)结合时,会诱导餐后胆囊体积出现不同的动态变化(P≤0.001)。对于酸稳定的乳剂,液滴尺寸减小2个数量级[LE1(0.33μm)与LE2(52μm)相比]会使胃排空延迟38分钟。尽管酸稳定(LE1和LE2)和可再分散(LE4)的乳剂会使血液甘油三酯持续升高,但LE3未检测到升高(P<0.0001)。对于LE3,MRI证实胃加工过程中会生成大的脂肪颗粒,这些颗粒排入小肠并在其中推进。
MRI能够详细描述脂质乳剂在体内的命运。脂质乳剂对胃排空、胆囊体积和甘油三酯吸收的急性作用取决于摄入过程中发生的微观结构变化。胃蠕动和分泌有效地使胃内的液态脂肪池再分散。该试验在clinicaltrials.gov上注册,注册号为NCT01253005。