| Literature DB >> 28550653 |
Janar Jenis1,2, Jeong Yoon Kim1, Zia Uddin1, Yeong Hun Song1, Hyeong-Hwan Lee1, Ki Hun Park3.
Abstract
Members of the genus Limonium are widely used as medicinal herbs due to their health-promoting effects, such as an ability to improve blood circulation by inhibiting angiotensin I converting enzyme (ACE). While the potential of L. michelsonii Lincz. (a medicinal plant endemic to Kazakhstan) to inhibit ACE has been demonstrated, the inhibitory activities of its secondary metabolites have not been explored. In this work, the principal phenolic compounds (1-20) among these metabolites were isolated to determine the components responsible for ACE inhibition. The natural abundances of the active constituents within the target plant were characterized by UPLC-Q-TOF/MS analysis. All of the isolated compounds except for gallates 10-12 were found to significantly inhibit ACE, with IC50 values of between 7.1 and 138.4 μM. Unexpectedly, the flavonol glycosides 16-20 were observed to be more potent than the corresponding aglycones 4 and 5. For example, quercetin (4) had IC50 = 30.3 μM, whereas its glycosides (16, 17) had IC50 = 10.2 and 14.5 μM, respectively. A similar trend was observed for myricetin (5) and its glycosides (18-20). In a kinetic study, the flavonols 3-5 and 16-20 and the dihydroflavonols 8 and 9 behaved as competitive inhibitors, whereas other flavones (1, 2, 13-15) and flavanones (6, 7) performed noncompetitive inhibition.Entities:
Keywords: Angiotensin I converting enzyme; Competitive inhibitors; Limonium michelsonii Lincz.; Phenolic metabolites
Mesh:
Substances:
Year: 2017 PMID: 28550653 DOI: 10.1007/s11418-017-1095-4
Source DB: PubMed Journal: J Nat Med ISSN: 1340-3443 Impact factor: 2.343