In vitro α-glucosidase inhibition and antioxidant activities of partially purified Antidesma bunius fruit and Gynura nepalensis leaf extracts.

Diabetes mellitus is a metabolic disorder characterized by increased blood glucose levels. Current treatments involve the use of sulfonylureas, α-glucosidase inhibitors, and other synthetic drugs. The study demonstrated the α-glucosidase inhibition and antioxidant properties of partially purified ethanolic extracts of Antidesma bunius fruits and Gynura nepalensis leaves, as possible herbal drug candidates. After ethanol extraction, the extracts were fractionated using normal phase liquid column chromatography, with elution solvents ethyl acetate, methanol and water. Fractionation resulted in five fractions for A. bunius (A1, A2, A3, A4 and A5) and seven fractions for G. nepalensis (G1, G2, G3, G4, G5, G6 and G7). Fraction G1 showed the highest α-glucosidase inhibition activity (90.61±8.05%) and possibly acted via a mixed mode of inhibition. For the antioxidant activities, Fraction A1 exhibited highest radical scavenging activity via DPPH assay (97.39±2.48%), Fraction G7 exhibited highest iron (II)-chelating activity (95.85±1.46%) and Fraction G6 exhibited highest ferric-ion reducing activity via FRAP assay (272.60 μg/mL FeSO4 equivalents). Phytochemical screening revealed that flavonoids and tannins were common among all fractions. The results demonstrated the potential of these plants as an antidiabetic herbal treatment. However, further studies needs to be done, specifically focusing on isolating the active component(s), structure and mechanism elucidation and toxicity assays.

Lignans from cultivated Gynura nepalensis / 中国中药杂志

Taking application of some isolation and purification technologies, including solvent extraction, rude solvent isolation, column chromatographies on silica gel and Sephadex LH-20 , and preparative HPLC , 4 compounds were obtained from Gynura nepalensis cultivated in a suburban area of Beijing. Their structures were identified by spectroscopic methods in conjunction with comparison of the NMR data with literature values as 7S,8R-9'-O-ethyl-dehydrodiconiferyl-9-acetate (1), 9'-O-ethyl-dehydrodiconiferyl alcohol (2), dehydrodiconiferyl-9,9'-diacetate(3), and (+)-medioresinol(4), respectively. 1 is a new 2,3-dihydrobenzofuran-8,3'-neolignane type compound, and 2-4 were isolated from G.nepalensis for the first time. The complete assignment of the 1H- and 13C-NMR spectroscopic data of the four compounds recorded in DMSO-d6 was achieved.