HPLC-MS/MS analysis, antioxidant and ?-amylase inhibitory activities of the endemic plant Ferula tunetana using in vitro and in silico methods

被引:11
作者
Baccari, Wiem [1 ]
Saidi, Ilyes [1 ]
Znati, Mansour [1 ]
Mustafa, Ahmed M. [2 ,3 ]
Caprioli, Giovanni [2 ]
Harrath, Abdel Halim [4 ]
Ben Jannet, Hichem [1 ]
机构
[1] Univ Monastir, Fac Sci Monastir, Team Med Chem & Nat Prod, Lab Heterocycl Chem Nat Prod & React,LR11ES39, Ave Environm, Monastir 5019, Tunisia
[2] Univ Camerino, Sch Pharm, Chem Interdisciplinary Project CHip, Via Madonna Carceri, I-62032 Camerino, Italy
[3] Zagazig Univ, Fac Pharm, Dept Pharmacognosy, Zagazig 44519, Egypt
[4] King Saud Univ, Coll Sci, Dept Zool, Riyadh 11451, Saudi Arabia
关键词
Ferula tunetana; HPLC-MS; MS; Antioxidant; Anti-?-amylase; Molecular docking; Drug-likeness prediction; CHEMICAL-COMPOSITION; VANILLIC ACID; ALPHA-AMYLASE; ASSA-FOETIDA; GENUS-FERULA; BIOACTIVITIES; POTENTIALS; FLAVONOIDS; EXTRACTS;
D O I
10.1016/j.procbio.2023.03.015
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
Ferula species have occupied great value in traditional medicine in various countries. The aim of the present paper was to assess for the first time to the phytochemical profile of Ferula tunetana Pomel ex Batt. (F. tunetana) seed and leaf extracts using HPLC-MS/MS, as well as to evaluate their antioxidant and anti-alpha-amylase activities. Therefore, total phenolic and flavonoid amounts of the studied extracts were determined and 38 compounds were detected and quantified (phenolic acids, flavonoids, non-phenolic acid and stilbenes). In addition of their antioxidant potential against 1,1-diphenyl-2-picrylhydrazyl (DPPH) and Ferric Reducing Antioxidant Power (FRAP) assays, in vitro and in silico studies were adopted to evaluate alpha-amylase inhibitory properties of F. tunetana extracts. Ethyl acetate (EtOAc) seed extract showed the highest total phenolic content, antioxidant potential (IC50 = 19.00 +/- 0.37 mu g/mL) in terms of free radical scavenging, also for alpha-amylase inhibition activity with IC50 values of 17.39 +/- 0.92 mu g/mL. The molecular docking analysis and the drug-likeness prediction of the major selected compounds explained the significant anti-alpha-amylase activity of the studied extracts. The obtained analysis and results suggest that F. tunetana extracts could be promising candidates to develop a new generation of efficient and especially safe antidiabetic treatments.
引用
收藏
页码:230 / 240
页数:11
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