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Phytosterols esterified with conjugated linoleic acid. in vitro intestinal digestion and interaction on cholesterol bioaccessibility

机译:植物固醇用共轭亚油酸酯化。体外肠道消化及其对胆固醇生物可及性的相互作用

摘要

Intestinal in vitro digestion of phytosterols esterified with conjugated linoleic acid (PS-CLA) was performed to study (1) the potential bioaccessibility of the released bioactive-lipid products and (2) the interference with cholesterol bioaccessibility. Commercial food-grade PS ester (PS-C) was assayed as reference. Hydrolysis of PS-CLA by digestive enzymes was similar to that of PS-C (51 and 47%, respectively), most lipids products being mainly included in the bioaccessible fraction, namely, the micellar phase (MP). Control assays in the absence of PS esters showed most cholesterol solubilized within the MP, whereas a displacement of total cholesterol was caused from MP after digestion of PS esters (14 and 36% displacement for PS-CLA and PS-C, respectively), cholesterol being partially precipitated. Precipitated cholesterol was linearly related to a parallel precipitation of saturated-chain PS, mainly determined by sitosterol (R 2 = 0.936). The higher composition in sitosteryl esters of PS-C with respect to PS-CLA might explain their different effects on cholesterol. Therefore, besides being a lipid delivery form of PS similar to other commercial esterified PS, the PS-CLA might have the additional advantage of being a lipid delivery form of CLA. Moreover, PS-CLA might hinder the bioaccessibility of cholesterol. Furthermore, the qualitative/quantitative profile in esterified PS forms might determine the magnitude of cholesterol interaction. © 2012 American Chemical Society.
机译:进行肠道体外消化共轭亚油酸(PS-CLA)酯化的植物甾醇的研究,以研究(1)释放的生物活性脂质产品的潜在生物利用度,以及(2)对胆固醇生物利用度的干扰。以商业食品级PS酯(PS-C)作为参考。消化酶对PS-CLA的水解与PS-C相似(分别为51%和47%),大多数脂质产物主要包含在生物可及级分中,即胶束相(MP)。在不存在PS酯的情况下的对照测定表明,大部分胆固醇在MP中溶解,而总胆固醇的置换是由PS酯消化后MP引起的(PS-CLA和PS-C分别置换14%和36%),胆固醇被部分沉淀。沉淀的胆固醇与饱和链PS的平行沉淀线性相关,主要由谷固醇测定(R 2 = 0.936)。相对于PS-CLA,PS-C的谷甾醇酯含量更高,可能解释了它们对胆固醇的不同作用。因此,除了是类似于其他市售酯化PS的PS脂质传递形式之外,PS-CLA可能还具有CLA脂质传递形式的额外优势。此外,PS-CLA可能会阻碍胆固醇的生物可及性。此外,酯化PS形式的定性/定量特征可能决定胆固醇相互作用的程度。 ©2012美国化学学会。

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