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首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Influence of human obesity on the metabolic fate of dietary long- and medium-chain triacylglycerols.
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Influence of human obesity on the metabolic fate of dietary long- and medium-chain triacylglycerols.

机译:人类肥胖对饮食中长链和三链甘油三酯代谢命运的影响。

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摘要

The metabolic fate of an oral long-chain-triacylglycerol (LCT) load and of a mixed oral LCT and medium-chain-triacylglycerol (MCT) load was followed for 6 h in eight control and eight obese subjects with normal postabsorptive triacylglycerol concentrations. Labeled triacylglycerol and indirect calorimetry were used. Results showed that LCTs were less oxidized in obese than in control subjects (3.2+/-0.5 compared with 6.0+/-0.4 g, P < 0.01). Moreover, the amount of LCT oxidized was negatively correlated with fat mass (r = -0.77, P < 0.01). Appearance in plasma of dietary triacyglycerol-derived long-chain fatty acids was blunted in obese subjects and it was negatively related to fat mass (r = -0.84, P < 0.01) and positively to LCT oxidation (r = 0.70, P < 0.01). On the contrary, MCT oxidation was not altered in obese subjects compared with control subjects. Furthermore, the proportion of MCTs oxidized was higher in both groups compared with LCTs (x+/-SEM: 57.5+/-2.6% compared with 15.2+/-1.6%, P < 0.01, n = 16). Our conclusion is that obesity is associated with a defect in the oxidation of dietary LCTs probably related to an excessive uptake by the adipose tissue of meal-derived long-chain fatty acids. MCTs, the oxidation of which is not altered in obesity, could therefore be of interest in the dietary treatment of obesity.
机译:在正常吸收后三酰甘油浓度的八名对照和八名肥胖受试者中,口服长链三酰基甘油(LCT)负荷以及口服LCT和中链三酰基甘油(MCT)混合负荷的代谢命运进行了6小时的追踪。使用标记的三酰基甘油和间接量热法。结果显示,与对照组相比,肥胖人群中LCT的氧化程度更低(3.2 +/- 0.5,而6.0 +/- 0.4 g,P <0.01)。此外,LCT的氧化量与脂肪量呈负相关(r = -0.77,P <0.01)。饮食中血浆甘油三酸酯来源的长链脂肪酸的外观变钝,与脂肪量呈负相关(r = -0.84,P <0.01),与LCT氧化呈正相关(r = 0.70,P <0.01) 。相反,与对照组相比,肥胖组的MCT氧化没有改变。此外,与LCT相比,两组中MCT的氧化比例均更高(x +/- SEM:57.5 +/- 2.6%,而15.2 +/- 1.6%,P <0.01,n = 16)。我们的结论是,肥胖与饮食中LCT的氧化缺陷有关,这可能与脂肪组织摄入的膳食中长链脂肪酸摄入过多有关。因此,在肥胖症的饮食治疗中,其氧化作用不会改变的MCTs可能会引起人们的兴趣。

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