黄酮类化合物抑制丙烯酰胺的动力学及作用位点
首发时间:2015-06-26
摘要:本研究探讨了黄酮类化合物抑制丙烯酰胺的动力学过程及作用位点。通过建立同步检测Maillard反应产物中天冬酰胺、葡萄糖、果糖和丙烯酰胺的同位素稀释超高效液相色谱-串联质谱(UHPLC-MS/MS)的检测方法,选取黄酮类化合物典型试样,在其最适剂量水平上建立土豆微波模式体系的Maillard反应六步动力学模型,观察天冬酰胺、葡萄糖、果糖、丙烯酰胺和类黑素的动力学变化,分析其抑制作用位点。结果表明,黄酮类化合物可显著地抑制天冬酰胺与果糖反应生成以Schiff碱为代表的中间产物的过程、葡萄糖通过异构化作用向果糖转化的过程以及中间产物向丙烯酰胺转化的过程,但无法抑制天冬酰胺与葡萄糖反应的过程和丙烯酰胺生成后的消除和转化过程。此外,黄酮类化合物对抑制Maillard反应终产物类黑素的形成有一定的影响,但这种作用并不显著。
关键词: 黄酮类化合物 抑制 丙烯酰胺 动力学 作用位点 超高效液相色谱-串联质谱
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Inhibitory effect of flavonoids on kinetics of acrylamide and related function sites
Abstract:Current work investigated the inhibitory effect of flavonoids on the kinetic process of acrylamide and related function sites. Initially, we developed an isotope dilution ultra high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) method for simultaneous determination of asparagine, glucose, fructose and acrylamide in Maillard reaction products. Considering characteristic types of flavonoids and their optimal levels for the reduction effect, we then established a six-step kinetic model for mimicking the Maillard reaction in a potato-based microwave heating model system. Finally, we observed kinetic profile changes of asparagine, glucose, fructose, acrylamide and melanoidins, and analyzed related function sites. Results indicated that flavonoids can significantly reduce the formation of intermediates such as Schiff base in the reaction between asparagine and fructose, the transform action from glucose to fructose via isomerization, and the formation of acrylamide from intermediates. However, they cannot reduce the reaction between asparagine and glucose and no effect on the elimination of acrylamide. In addition, flavonoids are capable of reducing the formation of melanoidins, which is one of final Maillard reaction products. However, such reduction effect seems not significant.
Keywords: Flavonoids Inhibition Acrylamide Kinetics Function sites UHPLC-MS/MS
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No.4648109107424914****
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