Borel P, Armand M, Pasquier B, Senft M, Dutot G, Melin C, Lafont H, Lairon D
Unité 130-INSERM (National Institute of Health and Medical Research), Marseille, France.
JPEN J Parenter Enteral Nutr. 1994 Nov-Dec;18(6):534-43. doi: 10.1177/0148607194018006534.
Assimilation of lipid nutrients depends on the efficiency of emulsified fat hydrolysis by digestive lipases. As shown in vitro, the activity of preduodenal and pancreatic lipases is governed by the physicochemical properties of emulsions. Thus the aim of this study was to evaluate in the rat how emulsions are digested and assimilated depending on their droplet size or solute composition. Fasted rats were intragastrically tube fed emulsions with different median droplet sizes (0.6 microns, fine; 22 microns, coarse) or solute composition (0.8 microns, complex fine) containing 14C-triolein and 3H-cholesterol. Two and 5 hours after feeding, fat-droplet size was measured in gastric and duodenal contents, and lipids were radioactively quantified in different compartments. In the stomach, the droplet size of the fine emulsions significantly increased to values (13 microns to 24 microns) comparable with those of the coarse emulsion (35 microns to 36 microns). In the duodenum, the droplet sizes of the three emulsions were in the range of 14 microns to 33 microns. After 2 hours, gastric triglyceride hydrolysis was significantly higher with the fine than with the coarse emulsion and was lower with the complex fine emulsion. Gastric emptying of fat was significantly different, with the following decreasing order: coarse, fine, and complex fine emulsion. In the small intestine, the fine and coarse emulsions were processed comparably, whereas the assimilation of the fine complex emulsion was significantly delayed. Calculations indicate that ingested fatty acids were distributed in the peripheral tissues at different rates with the same decreasing order. The fate of a lipophilic nutrient, cholesterol, was also markedly altered by the type of emulsion. These data support the concept that tube-fed emulsions with different droplet sizes and solute composition are digested differently and thus are metabolized differently.
脂质营养素的吸收取决于消化脂肪酶对乳化脂肪的水解效率。体外实验表明,十二指肠前脂肪酶和胰脂肪酶的活性受乳剂物理化学性质的影响。因此,本研究的目的是评估在大鼠体内,乳剂如何根据其液滴大小或溶质组成进行消化和吸收。禁食的大鼠通过胃管饲法给予含有14C-三油酸甘油酯和3H-胆固醇的不同中位液滴大小(0.6微米,细;22微米,粗)或溶质组成(0.8微米,复合细)的乳剂。喂食后2小时和5小时,测量胃和十二指肠内容物中的脂肪滴大小,并对不同隔室中的脂质进行放射性定量。在胃中,细乳剂的液滴大小显著增加至与粗乳剂(35微米至36微米)相当的值(13微米至24微米)。在十二指肠中,三种乳剂的液滴大小在14微米至33微米范围内。2小时后,细乳剂的胃甘油三酯水解明显高于粗乳剂,而复合细乳剂的胃甘油三酯水解较低。脂肪的胃排空存在显著差异,顺序为:粗乳剂、细乳剂、复合细乳剂。在小肠中,细乳剂和粗乳剂的处理方式相当,而复合细乳剂的吸收明显延迟。计算表明,摄入的脂肪酸以相同的递减顺序以不同速率分布在外周组织中。亲脂性营养素胆固醇的命运也因乳剂类型而显著改变。这些数据支持了这样的概念,即经胃管饲的具有不同液滴大小和溶质组成的乳剂消化方式不同,因此代谢方式也不同。