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When cholesterol is not cholesterol: a note on the enzymatic determination of its concentration in model systems containing vegetable extracts

机译:当胆固醇不是胆固醇时:在含有植物提取物的模型系统中酶法测定其浓度的注意事项

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Background Experimental evidences demonstrate that vegetable derived extracts inhibit cholesterol absorption in the gastrointestinal tract. To further explore the mechanisms behind, we modeled duodenal contents with several vegetable extracts. Results By employing a widely used cholesterol quantification method based on a cholesterol oxidase-peroxidase coupled reaction we analyzed the effects on cholesterol partition. Evidenced interferences were analyzed by studying specific and unspecific inhibitors of cholesterol oxidase-peroxidase coupled reaction. Cholesterol was also quantified by LC/MS. We found a significant interference of diverse (cocoa and tea-derived) extracts over this method. The interference was strongly dependent on model matrix: while as in phosphate buffered saline, the development of unspecific fluorescence was inhibitable by catalase (but not by heat denaturation), suggesting vegetable extract derived H2O2 production, in bile-containing model systems, this interference also comprised cholesterol-oxidase inhibition. Several strategies, such as cholesterol standard addition and use of suitable blanks containing vegetable extracts were tested. When those failed, the use of a mass-spectrometry based chromatographic assay allowed quantification of cholesterol in models of duodenal contents in the presence of vegetable extracts. Conclusions We propose that the use of cholesterol-oxidase and/or peroxidase based systems for cholesterol analyses in foodstuffs should be accurately monitored, as important interferences in all the components of the enzymatic chain were evident. The use of adequate controls, standard addition and finally, chromatographic analyses solve these issues.
机译:背景技术实验证据表明,植物提取物可抑制胃肠道中的胆固醇吸收。为了进一步探索背后的机制,我们用几种蔬菜提取物对十二指肠内容物进行了建模。结果通过采用基于胆固醇氧化酶-过氧化物酶偶联反应的广泛使用的胆固醇定量方法,我们分析了对胆固醇分配的影响。通过研究胆固醇氧化酶-过氧化物酶偶联反应的特异性和非特异性抑制剂,分析了明显的干扰。胆固醇也通过LC / MS定量。我们发现,该方法对各种(可可和茶衍生的)提取物产生了重大干扰。干扰强烈依赖于模型基质:虽然在磷酸盐缓冲液中,过氧化氢酶可抑制非特异性荧光的发展(但不能通过热变性),这表明在含胆汁的模型系统中植物提取物产生的H2O2产生,这种干扰也包括抑制胆固醇氧化酶。测试了几种策略,例如添加胆固醇标准品和使用含有蔬菜提取物的空白剂。当这些方法失败时,使用基于质谱的色谱分析法可在存在蔬菜提取物的情况下对十二指肠内容物模型中的胆固醇进行定量。结论我们建议应精确监控在食品中胆固醇分析中使用的基于胆固醇氧化酶和/或过氧化物酶的系统,因为明显干扰了酶链的所有成分。使用适当的对照,标准添加物以及最后的色谱分析解决了这些问题。

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