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在脂肪吸收不良大鼠模型中,结构甘油三酯与物理混合物的淋巴吸收情况

Lymphatic absorption of structured triglycerides vs. physical mix in a rat model of fat malabsorption.

作者信息

Tso P, Lee T, Demichele S J

机构信息

Department of Pathology, University of Cincinnati Medical Center, Cincinnati 45267, Ohio, USA.

出版信息

Am J Physiol. 1999 Aug;277(2):G333-40. doi: 10.1152/ajpgi.1999.277.2.G333.

Abstract

Comparison was made between the intestinal absorption and lymphatic transport of a randomly interesterified fish oil and medium-chain triglyceride (MCT) structured triglycerides (STG) vs. the physical mix in rat small intestine following ischemia and reperfusion (I/R) injury. Under halothane anesthesia, the superior mesenteric artery (SMA) was occluded for 20 min and then reperfused in I/R rats. The SMA was isolated but not occluded in control rats. In both treatment groups, the mesenteric lymph duct was cannulated and a gastric tube was inserted. Each treatment group received 1 ml of the fish oil-MCT STG or physical mix (7 rats/group) through the gastric tube followed by an infusion of PBS at 3 ml/h for 8 h. Lymph was collected hourly for 8 h. Lymph triglyceride, cholesterol, and decanoic and eicosapentaenoic acids increased rapidly and maintained a significantly higher output (P < 0.01) with STG compared with physical mix in control rats over 8 h. After I/R, lymphatic triglyceride output decreased 50% compared with control. Gastric infusion of STG significantly improved lipid transport by having a twofold higher triglyceride, cholesterol, and decanoic and eicosapentaenoic acids output to lymph compared with its physical mix (P < 0.01). We conclude that STG is absorbed into lymph significantly better than physical mix by both the normal intestine and the intestine injured by I/R.

摘要

比较了随机酯交换鱼油和中链甘油三酯(MCT)结构甘油三酯(STG)与物理混合物在大鼠小肠缺血再灌注(I/R)损伤后的肠道吸收和淋巴转运情况。在氟烷麻醉下,对I/R大鼠的肠系膜上动脉(SMA)进行20分钟的阻断,然后再灌注。对照组大鼠分离出SMA但不进行阻断。在两个治疗组中,均对肠系膜淋巴管进行插管并插入胃管。每个治疗组通过胃管给予1 ml鱼油-MCT STG或物理混合物(每组7只大鼠),随后以3 ml/h的速度输注PBS,持续8小时。每小时收集淋巴液,共收集8小时。在对照大鼠中,与物理混合物相比,STG使淋巴甘油三酯、胆固醇、癸酸和二十碳五烯酸迅速增加,并在8小时内维持显著更高的输出量(P<0.01)。I/R后,淋巴甘油三酯输出量比对照降低了50%。与物理混合物相比,胃内输注STG使淋巴中甘油三酯、胆固醇、癸酸和二十碳五烯酸的输出量提高了两倍,显著改善了脂质转运(P<0.01)。我们得出结论,无论是正常肠道还是I/R损伤的肠道,STG被吸收进入淋巴的效果都明显优于物理混合物。

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