Department of Biology, School of Science and Technology, Sefako Makgatho Health Science University, Molotlegi Street, Ga-Rankuwa, Pretoria 0204, South Africa.
Natural Product Research Group, Department of Pharmacy, Faculty of Science, Tadulako University, Palu-Central Sulawesi 94118, Indonesia.
Molecules. 2022 May 16;27(10):3175. doi: 10.3390/molecules27103175.
, a medicinal plant with ethnopharmacology use, has a dearth of information regarding its antidiabetic properties. This study evaluated the crude methanol leaf extract of and its fractions for total phenolic content, antioxidant activity, and digestive enzymes (α-amylase and α-glucosidase) inhibitory activity using standard methods. The total phenolic content (56.53 ± 1.94 mg GAE/g dry extract) and DPPH Trolox antioxidant equivalent (TAE) (1.51 ± 0.66 µg/mL) of the methanol fraction were the highest among the fractions. The IC values of the methanol fraction against α-amylase (10.76 ± 1.33 µg/mL) and α-glucosidase (12.25 ± 1.05 µg/mL) activities were also high. Being the most active, the methanol fraction was subjected to bio-assay guided column chromatography-based enzyme inhibition to obtain a pure compound. The phenolic compound isolated and identified as naringenin inhibited α-amylase and α-glucosidase with IC of 5.81 ± 2.14 µg/mL and 4.77 ± 2.99 µg/mL, respectively. This is the first study to isolate naringenin from extract. The molecular docking and molecular dynamics studies demonstrated naringenin as a promising lead compound in comparison to acarbose for the treatment of diabetes through the inhibition of α-glucosidase activity.
,一种具有民族药理学用途的药用植物,其抗糖尿病特性的信息匮乏。本研究采用标准方法评估了 的甲醇叶粗提物及其馏分的总酚含量、抗氧化活性和消化酶(α-淀粉酶和α-葡萄糖苷酶)抑制活性。甲醇馏分的总酚含量(56.53 ± 1.94 mg GAE/g 干提取物)和 DPPH Trolox 抗氧化等效物(TAE)(1.51 ± 0.66 µg/mL)在馏分中最高。甲醇馏分对α-淀粉酶(10.76 ± 1.33 µg/mL)和α-葡萄糖苷酶(12.25 ± 1.05 µg/mL)活性的 IC 值也很高。甲醇馏分是最活跃的,因此进行了基于生物测定指导的柱层析的酶抑制实验,以获得纯化合物。分离并鉴定为柚皮素的酚类化合物对α-淀粉酶和α-葡萄糖苷酶的抑制作用的 IC 分别为 5.81 ± 2.14 µg/mL 和 4.77 ± 2.99 µg/mL。这是首次从 提取物中分离出柚皮素的研究。分子对接和分子动力学研究表明,与阿卡波糖相比,柚皮素作为一种有前途的先导化合物,通过抑制α-葡萄糖苷酶活性,可用于治疗糖尿病。