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首页> 外文期刊>Food & Function >Quantification of 4-hydroxy-2-nonenal-protein adducts in the in vivo gastric digesta of mini-pigs using a GC-MS/MS method with accuracy profile validation
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Quantification of 4-hydroxy-2-nonenal-protein adducts in the in vivo gastric digesta of mini-pigs using a GC-MS/MS method with accuracy profile validation

机译:使用GC-MS / MS方法对小型猪的体内胃消化物中的4-羟基-2-壬醛蛋白加合物进行定量并验证准确性

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摘要

Hydroxyalkenals are lipid oxidation end-products resulting from the oxidation of polyunsaturated fatty acids (PUFA). This study aimed at quantifying the production of 4-hydroxy-2-nonenal-protein adducts (HNE-P) via Michael addition from n-6 PUFA oxidation in the gastric digesta of mini-pigs after the consumption of meat-based meals with different plant antioxidant contents. Using the accuracy profile procedure, we validated an extraction protocol for the quantification of HNE-P by GC-MS/ MS in gastric contents. The formation of HNE-P in the gastric compartment was observed for the first time, with concentrations ranging from less than 0.52 to 1.33 nmol HNE-P per 500 mg digesta. Nevertheless, most gastric HNE-P levels were below the limit of quantification of 0.52 nmol HNE-P per 500 mg digesta. In this animal study, the protective effect of plant antioxidant sources on HNE-P formation was not evidenced contrasting with the results using TBARS as markers.
机译:羟基缩酮是多不饱和脂肪酸(PUFA)氧化产生的脂质氧化终产物。这项研究旨在通过食用不同肉类食物后,通过小型猪的胃消化物中n-6 PUFA氧化过程中通过迈克尔加成反应产生的n-6 PUFA氧化来定量产生4-羟基-2-壬烯蛋白加合物(HNE-P)。植物抗氧化剂含量。使用准确度分析程序,我们验证了通过GC-MS / MS对胃内容物中HNE-P进行定量的提取方案。首次观察到胃腔内HNE-P的形成,其浓度范围为每500 mg消化物少于0.52至1.33 nmol HNE-P。然而,大多数胃HNE-P水平低于每500 mg消化物0.52 nmol HNE-P的定量极限。在这项动物研究中,没有发现植物抗氧化剂对HNE-P形成的保护作用与使用TBARS作为标记物的结果形成对比。

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