The inhibitory Effects of Some Artificial Food Colorings on α-amylase and α-glucosidase: In Vitro and In Silico Studies

Q4 Pharmacology, Toxicology and Pharmaceutics
Reguia Mahfoudi, A. Djeridane, D. Tahri, M. Yousfi
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引用次数: 0

Abstract

Inhibition of α-amylase and α-glucosidase is considered as an important therapeutic target to manage type 2 diabetes mellitus (T2DM), reducing postprandial hyperglycemia (PPHG). The present work explored the antidiabetic activities of five artificial food colorings by α-amylase and α-glucosidase enzyme inhibition in vitro and in Silico. In this study, inhibition of α-amylase and α-glucosidase were evaluated. Further, the interaction between enzymes (α-amylase and α-glucosidase) and ligands (food colorings) was followed by QSAR and molecular docking studies. The in vitro results obtained show that the blue patent (SIN131) exhibited more potent inhibition with IC50 values of 0.03± 0.01 mM and 0.014±0.001 mM against α-amylase and α-glucosidase inhibition respectively compared to acarbose. The QSAR study found a strong correlation between IC50 values with four molecular descriptors. This linear regression confirms that a strong polarity (Apol) and a low hydrophobia (ALogP) favor the inhibitory effect of these colorings toward both enzymes. Also, a negative role of the number of heavy atoms has been demonstrated in the phenomenon of inhibition of this enzyme. Finally, the descriptor εlumo (electronic affinity) plays a crucial role on the inhibitory power of these dyes toward both enzymes by electron transfer. The virtual screening of the inhibition of α-amylase and α-glucosidase by these colorings, using Molegro Virtual Docker (MVD), allowed us to obtain stable complexes with interaction energies resulting from the place of hydrogen bonds and several hydrophobic interactions. However, the sulfonate groups of these colorings can be the major factors in the inhibition of these enzymes. On the other hand, Rerank Score with the pose are perfectly correlated (R2> 0.76) to the inhibitory activity of these food colorings measured experimentally. The present study suggests that the Blue Patent V (SIN131) effectively act as α-amylase and α-glucosidase inhibitor leading to a reduction in starch hydrolysis and hence eventually to lowered glucose levels.
几种人工色素对α-淀粉酶和α-葡萄糖苷酶的抑制作用:体外和Silico研究
抑制α-淀粉酶和α-葡萄糖苷酶被认为是控制2型糖尿病(T2DM)、降低餐后高血糖(PPHG)的重要治疗靶点。本文通过α-淀粉酶和α-葡萄糖苷酶对5种人工食用色素的体外和体外抗糖尿病活性进行了研究。本研究对α-淀粉酶和α-葡萄糖苷酶的抑制作用进行了评价。此外,酶(α-淀粉酶和α-葡萄糖苷酶)与配体(食用色素)之间的相互作用通过QSAR和分子对接研究进行了跟踪。体外实验结果表明,与阿卡波糖相比,蓝色专利(SIN131)对α-淀粉酶和α-葡萄糖苷酶的IC50分别为0.03±0.01 mM和0.014±0.001 mM,具有较强的抑制作用。QSAR研究发现,IC50值与四种分子描述符之间存在很强的相关性。这种线性回归证实了强极性(Apol)和低疏水性(ALogP)有利于这些着色剂对这两种酶的抑制作用。此外,重原子数的负作用已被证明在抑制这种酶的现象。最后,描述子εlumo(电子亲和)在染料通过电子转移对两种酶的抑制能力中起着至关重要的作用。利用Molegro virtual Docker (MVD)虚拟筛选这些着色剂对α-淀粉酶和α-葡萄糖苷酶的抑制作用,使我们能够获得稳定的配合物,其相互作用能来自氢键的位置和几种疏水相互作用。然而,这些着色剂的磺酸基可能是抑制这些酶的主要因素。另一方面,实验测量的这些食用色素的抑制活性与姿势的Rerank Score完全相关(R2> 0.76)。目前的研究表明,蓝色专利V (SIN131)有效地作为α-淀粉酶和α-葡萄糖苷酶抑制剂,导致淀粉水解减少,从而最终降低葡萄糖水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Enzyme Inhibition
Current Enzyme Inhibition Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.30
自引率
0.00%
发文量
30
期刊介绍: Current Enzyme Inhibition aims to publish all the latest and outstanding developments in enzyme inhibition studies with regards to the mechanisms of inhibitory processes of enzymes, recognition of active sites, and the discovery of agonists and antagonists, leading to the design and development of new drugs of significant therapeutic value. Each issue contains a series of timely, in-depth reviews written by leaders in the field, covering a range of enzymes that can be exploited for drug development. Current Enzyme Inhibition is an essential journal for every pharmaceutical and medicinal chemist who wishes to have up-to-date knowledge about each and every development in the study of enzyme inhibition.
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