Department of Biotechnology and Bioinformatics, School of Life Sciences, JSS Academy of Higher Education and Research, Mysuru 570015, Karnataka, India.
Biology Department, Faculty of Science, University of Tabuk, Tabuk 71491, Saudi Arabia.
Molecules. 2022 Mar 14;27(6):1888. doi: 10.3390/molecules27061888.
For the first time, α-glucosidase, α-amylase, aldose reductase, and glycation at multiple stages inhibitory assays were used to explore the antidiabetic potential of whole unripe jackfruit (peel with pulp, flake, and seed). Two polyphenols (phenolic acids) with strong antihyperglycaemic activity were isolated from the methanol extract of whole jackfruit flour (MJ) using activity-guided repeated fractionation on a silica gel column chromatography. The bioactive compounds isolated were identified as 3-(3,4-Dihydroxyphenyl)-2-propenoic acid (caffeic acid: CA) and 4-Hydroxy-3,5-dimethoxybenzoic acid (syringic acid: SA) after various physicochemical and spectroscopic investigations. CA (IC: 8.0 and 26.90 µg/mL) and SA (IC: 7.5 and 25.25 µg/mL) were identified to inhibit α-glucosidase and α-amylase in a competitive manner with low Ki values. In vitro glycation experiments further revealed that MJ and its components inhibited each stage of protein glycation as well as the generation of intermediate chemicals. Furthermore, CA (IC: 3.10) and SA (IC: 3.0 µg/mL) inhibited aldose reductase effectively in a non-competitive manner, respectively. The binding affinity of these substances towards the enzymes examined has been proposed by molecular docking and molecular dynamics simulation studies, which may explain their inhibitory activities. The found potential of MJ in antihyperglycaemic activity via inhibition of α-glucosidase and in antidiabetic action via inhibition of the polyol pathway and protein glycation is more likely to be related to the presence of the phenolic compounds, according to our findings.
首次采用α-葡萄糖苷酶、α-淀粉酶、醛糖还原酶和糖化多阶段抑制试验来探索整个未成熟菠萝(果皮带果肉、薄片和种子)的降血糖潜力。从整个菠萝粉(MJ)的甲醇提取物中,使用硅胶柱色谱的活性导向重复分段法分离出两种具有很强降血糖活性的多酚(酚酸)。经多种物理化学和光谱研究,分离出的生物活性化合物被鉴定为 3-(3,4-二羟基苯基)-2-丙烯酸(咖啡酸:CA)和 4-羟基-3,5-二甲氧基苯甲酸(丁香酸:SA)。CA(IC:8.0 和 26.90 µg/mL)和 SA(IC:7.5 和 25.25 µg/mL)被鉴定为以竞争性方式抑制α-葡萄糖苷酶和α-淀粉酶,具有低 Ki 值。体外糖化实验进一步表明,MJ 及其成分抑制蛋白质糖化的各个阶段以及中间化学物质的产生。此外,CA(IC:3.10)和 SA(IC:3.0 µg/mL)分别以非竞争性方式有效抑制醛糖还原酶。通过分子对接和分子动力学模拟研究提出了这些物质对所检查的酶的结合亲和力,这可能解释了它们的抑制活性。根据我们的发现,MJ 在通过抑制α-葡萄糖苷酶发挥降血糖活性以及通过抑制多元醇途径和蛋白质糖化发挥抗糖尿病作用的潜力,很可能与酚类化合物的存在有关。