Alchemilla viridiflora Rothm.: the potent natural inhibitor of angiotensin I-converting enzyme

被引:9
|
作者
Radovic, Jelena [1 ]
Surucic, Relja [2 ]
Niketic, Marjan [3 ]
Kundakovic-Vasovic, Tatjana [1 ]
机构
[1] Univ Belgrade, Dept Pharmacognosy, Fac Pharm, Belgrade, Serbia
[2] Univ Banja Luka, Dept Pharmacognosy, Fac Med, Banja Luka, Bosnia & Herceg
[3] Nat Hist Museum, Njegoseva 51, Belgrade, Serbia
关键词
Alchemilla viridiflora; Chemical composition; Ellagitannins; Flavonoids; ACE inhibitors; FLAVONOID GLYCOSIDES; ANTIMICROBIAL ACTIVITIES; ANTIOXIDANT; VULGARIS; VASORELAXANT; ACID; CONSTITUENTS; METABOLITES; METHANOL;
D O I
10.1007/s11010-022-04410-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alchemilla viridiflora Rothm., Rosaceae is a herbaceous plant widespread in central Greece, Bulgaria, North Macedonia and Serbia with Kosovo. Liquid chromatography-mass spectrometry analysis leads to the identification of 20 compounds in methanol extract, mainly ellagitannins and flavonoid glycosides. Given that various plant extracts have traditionally been used to treat hypertension and that some of the analyzed methanol extract constituents have beneficial cardiovascular effects, we hypothesized that some of these effects are achieved by inhibiting angiotensin I-converting enzyme (ACE). The dose-dependent ACE inhibitory activities of A. viridiflora and miquelianin were observed with an IC50 of 2.51 +/- 0.00 mu g/mL of A. viridiflora extract compared to the IC50 of 5.4139 +/- 0.00 mu M for miquelianin. The contribution of the single compounds to the tested activity was further analyzed through the in silico experimental approach. Computational docking results showed that tiliroside, ellagic acid pentose and galloyl-hexahydroxydiphenoyl-glucose exhibited even better binding affinity for the ACE active site than miquelianin, for which ACE activity was confirmed by an in vitro assay.
引用
收藏
页码:1893 / 1903
页数:11
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