Barks of Three Wild Pyrus Taxa: Phenolic Constituents, Antioxidant Activity, and in Vitro and in Silico Investigations of α-Amylase and α-Glucosidase Inhibition

被引:5
|
作者
Usjak, Ljubos J. [1 ]
Milutinovic, Violeta M. [1 ]
Crnogorac, Marija J. Dordic [2 ]
Stanojkovic, Tatjana P. [2 ]
Niketic, Marjan S. [3 ]
Kukic-Markovic, Jelena M. [1 ]
Petrovic, Silvana D. [1 ]
机构
[1] Univ Belgrade, Dept Pharmacognosy, Fac Pharm, Vojvode Stepe 450, Belgrade 11221, Serbia
[2] Inst Oncol & Radiol Serbia, Pasterova 14, Belgrade 11000, Serbia
[3] Nat Hist Museum, Njegoseva 51, Belgrade 11000, Serbia
关键词
three wild Pyrus taxa; bark dry extracts; liquid chromatography; biological activity; molecular docking; TRADITIONAL USE; EXTRACTS; ARBUTIN; PROCYANIDINS; SERBIA; PLANTS;
D O I
10.1002/cbdv.202100446
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dry MeOH extracts of the twig barks of Pyrus communis subsp. pyraster, P. spinosa and their hybrid P.xjordanovii nothosubsp. velenovskyi, collected in wild in Serbia, were analyzed. By LC/MS, the contents of arbutin (99.9-131.0 mg/g), chlorogenic acid (2.2-6.3 mg/g), catechin (1.0-5.3 mg/g) and total dimeric and trimeric procyanidins (42.2-61.3 mg/g), including procyanidin B2 (8.9-17.2 mg/g), were determined. Colorimetrically, high contents of total phenolics (436.2-533.4 mg GAE/g) and tannins (339.4-425.7 mg GAE/g), as well as strong total antioxidant activities (FRAP values 4.5-5.9 mmol Fe2+/g), and DPPH (SC50=6.6-7.1 mu g/ml) and hydroxyl radical (SC50=447.1-727.7 mu g/ml) scavenging abilities were revealed. In vitro, all extracts exhibited notable inhibition of alpha-amylase (IC50=310.8-617.7 mu g/ml) and particularly strong inhibition of alpha-glucosidase (IC50=2.1-3.7 mu g/ml). Molecular docking predicted that among identified compounds procyanidin B2 is the best inhibitor of these carbohydrate-digesting enzymes. Obtained results showed that the barks of investigated Pyrus hybrid and its parent taxa have similar composition and bioactivity.
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