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利用体外和计算机模拟方法洞察龙胆酸的抗糖尿病潜力。

Insight into Gentisic Acid Antidiabetic Potential Using In Vitro and In Silico Approaches.

作者信息

Mechchate Hamza, Es-Safi Imane, Mohamed Al Kamaly Omkulthom, Bousta Dalila

机构信息

Laboratory of Biotechnology, Environment, Agrifood, and Health, Department of Biology, University of Sidi Mohamed Ben Abdellah, FSDM-Fez 30050, Morocco.

Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh 11564, Saudi Arabia.

出版信息

Molecules. 2021 Mar 30;26(7):1932. doi: 10.3390/molecules26071932.

Abstract

Numerous scientific studies have confirmed the beneficial therapeutic effects of phenolic acids. Among them gentisic acid (GA), a phenolic acid extensively found in many fruit and vegetables has been associated with an enormous confirmed health benefit. The present study aims to evaluate the antidiabetic potential of gentisic acid and highlight its mechanisms of action following in silico and in vitro approaches. The in silico study was intended to predict the interaction of GA with eight different receptors highly involved in the management and complications of diabetes (dipeptidyl-peptidase 4 (DPP4), protein tyrosine phosphatase 1B (PTP1B), free fatty acid receptor 1 (FFAR1), aldose reductase (AldR), glycogen phosphorylase (GP), α-amylase, peroxisome proliferator-activated receptor gamma (PPAR-γ) and α-glucosidase), while the in vitro study studied the potential inhibitory effect of GA against α-amylase and α-glucosidase. The results indicate that GA interacted moderately with most of the receptors and had a moderate inhibitory activity during the in vitro tests. The study therefore encourages further in vivo studies to confirm the given results.

摘要

众多科学研究已证实酚酸具有有益的治疗效果。其中龙胆酸(GA),一种广泛存在于许多水果和蔬菜中的酚酸,已被证实具有巨大的健康益处。本研究旨在评估龙胆酸的抗糖尿病潜力,并通过计算机模拟和体外实验方法突出其作用机制。计算机模拟研究旨在预测GA与八种在糖尿病管理和并发症中高度相关的不同受体(二肽基肽酶4(DPP4)、蛋白酪氨酸磷酸酶1B(PTP1B)、游离脂肪酸受体1(FFAR1)、醛糖还原酶(AldR)、糖原磷酸化酶(GP)、α-淀粉酶、过氧化物酶体增殖物激活受体γ(PPAR-γ)和α-葡萄糖苷酶)的相互作用,而体外研究则研究了GA对α-淀粉酶和α-葡萄糖苷酶的潜在抑制作用。结果表明,GA在体外实验中与大多数受体有适度相互作用,并具有适度的抑制活性。因此,该研究鼓励进一步开展体内研究以证实上述结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/707e/8037080/f79a8ab389f6/molecules-26-01932-g001.jpg

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