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Fluorescence interference of polyphenols in assays screening for dipeptidyl peptidase IV inhibitory activity

机译:二肽基肽酶IV抑制活性的测定筛选中多酚的荧光干扰

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摘要

Abstract Polyphenols are plant‐derived natural compounds, which are attributed to various beneficial effects on human health. Therefore, they are extensively investigated in different experimental setups. These compounds exhibit favorable antidiabetic effects in various clinical trials. However, their mode of action is not completely elucidated. A potential molecular target of certain polyphenols could be the dipeptidyl peptidase IV (DPP IV). This enzyme is abundant in human serum and represents a serine exopeptidase that cleaves and thus rapidly deactivates incretin hormones which are responsible for adequate postprandial insulin secretion from the pancreas. Multiple inhibitors of DPP IV have already been approved as antidiabetic drugs. In the course of screening assays exploring in vitro DPP IV inhibitory activities of polyphenols, some implausible observations prompted a detailed analysis of the interaction of polyphenols with fluorescence signals. The results revealed that quercetin quenched the fluorescence intensity, while 6‐methoxyflavone and urolithin B enhanced fluorescence signals depending on particular experimental conditions such as solvent composition. Thus, individual polyphenols might conflict with the experimental setup of fluorescence‐based DPP IV inhibitor screening assays. To avoid false positive or false negative results, polyphenols under investigations should be carefully controlled for potential assay interferences.
机译:摘要多酚是植物衍生的天然化合物,这是由于对人体健康的各种有益效果。因此,它们被广泛地应用于不同的实验设置研究。这些化合物显示出在不同的临床试验中有利抗糖尿病作用。然而,它们的作用模式尚未完全阐明。某些多酚的潜在分子靶标可以是二肽基肽IV(DPP IV)。这种酶是人血清中丰富,并代表丝氨酸外肽酶裂解,从而迅速地失活肠降血糖素激素,其负责从胰腺充足餐后胰岛素分泌。 DPP IV的多种抑制剂已经被批准为降糖药。在筛选测定中的多酚的体外DPP IV抑制活性探索的过程中,一些难以置信的观察提示荧光信号多酚的相互作用的详细分析。结果表明,槲皮素淬灭的荧光强度,而这取决于特定的实验条件,如溶剂组合物6-methoxyflavone和urolithin乙增强的荧光信号。因此,从个人多酚可能与基于荧光的DPP IV抑制剂筛选测定的实验装置冲突。为避免假阳性或假阴性结果,调查下多酚应小心控制潜在的分析干扰。

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