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Alpha-Amylase and Alpha-Glucosidase Enzyme Inhibition and Antioxidant Potential of 3-Oxolupenal and Katononic Acid Isolated from Nuxia oppositifolia

机译:怒霞的3-羟戊烯醛和酮酸对α-淀粉酶和α-葡糖苷酶的抑制及抗氧化能力

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摘要

is traditionally used in diabetes treatment in many Arabian countries; however, scientific evidence is lacking. Hence, the present study explored the antidiabetic and antioxidant activities of the plant extracts and their purified compounds. The methanolic crude extract of was partitioned using a two-solvent system. The -hexane fraction was purified by silica gel column chromatography to yield several compounds including katononic acid and 3-oxolupenal. Antidiabetic activities were assessed by α-amylase and α-glucosidase enzyme inhibition. Antioxidant capacities were examined by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) scavenging assays. Further, the interaction between enzymes (α-amylase and α-glucosidase) and ligands (3-oxolupenal and katononic acid) was followed by fluorescence quenching and molecular docking studies. 3-oxolupenal and katononic acid showed IC values of 46.2 μg/mL (101.6 µM) and 52.4 μg/mL (119.3 µM), respectively against the amylase inhibition. 3-oxolupenal (62.3 µg/mL or 141.9 μM) exhibited more potent inhibition against α-glucosidases compared to katononic acid (88.6 µg/mL or 194.8 μM). In terms of antioxidant activity, the relatively polar crude extract and -butanol fraction showed the greatest DPPH and ABTS scavenging activity. However, the antioxidant activities of the purified compounds were in the low to moderate range. Molecular docking studies confirmed that 3-oxolupenal and katononic acid interacted strongly with the active site residues of both α-amylase and α-glucosidase. Fluorescence quenching results also suggest that 3-oxolupenal and katononic acid have a good affinity towards both α-amylase and α-glucosidase enzymes. This study provides preliminary data for the plant’s use in the treatment of type 2 diabetes mellitus.
机译:传统上在许多阿拉伯国家/地区用于糖尿病治疗;但是,缺乏科学证据。因此,本研究探索了植物提取物及其纯化的化合物的抗糖尿病和抗氧化活性。用两溶剂系统分配甲醇的甲醇粗提物。通过硅胶柱色谱法纯化-己烷级分,得到几种化合物,包括tononic acid和3-oxolupenal。通过α-淀粉酶和α-葡萄糖苷酶的抑制作用来评估抗糖尿病活性。通过2,2-二苯基-1-吡啶并肼基(DPPH)和2,2′-叠氮基双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)清除测定法检测抗氧化能力。此外,酶(α-淀粉酶和α-葡糖苷酶)与配体(3-氧戊烯醛和酮酸)之间的相互作用随后进行了荧光猝灭和分子对接研究。 3-氧丙戊醛和刀豆酸对淀粉酶的抑制作用的IC值分别为46.2μg/ mL(101.6 µM)和52.4μg/ mL(119.3 µM)。与酮酸(88.6 µg / mL或194.8μM)相比,3-氧丙戊醛(62.3 µg / mL或141.9μM)对α-葡萄糖苷酶表现出更强的抑制作用。就抗氧化剂活性而言,相对极性的粗提物和-丁醇馏分显示出最大的DPPH和ABTS清除活性。然而,纯化的化合物的抗氧化活性在低至中等范围内。分子对接研究证实,3-氧戊烯醛和刀豆酸与α-淀粉酶和α-葡萄糖苷酶的活性位点残基强烈相互作用。荧光猝灭的结果还表明3-氧戊烯醛和钾酸对α-淀粉酶和α-葡糖苷酶都具有良好的亲和力。这项研究提供了该植物用于治疗2型糖尿病的初步数据。

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