Olive Leaf Extracts Are a Natural Source of Advanced Glycation End Product Inhibitors

Advanced glycation end products (AGEs), which are readily formed and accumulated with sustained hyperglycemia,contribute to the development of diabetic complications. As a consequence, inhibition of AGE formation constitutes an attractive therapeutic/preventive target. In the current study, we explo...

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Veröffentlicht in:Journal of medicinal food 2013, 16(9), , pp.817-822
Hauptverfasser: Vassiliki G. Kontogianni, Pantelis Charisiadis, Evangelia Margianni, Fotini N. Lamari, Ioannis P. Gerothanassis, Andreas G. Tzakos
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Sprache:eng
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Zusammenfassung:Advanced glycation end products (AGEs), which are readily formed and accumulated with sustained hyperglycemia,contribute to the development of diabetic complications. As a consequence, inhibition of AGE formation constitutes an attractive therapeutic/preventive target. In the current study, we explored the phytochemical composition and the in vitro effect of two different olive leaf extracts (an aqueous and a methanolic) on AGE formation. The methanolic olive leaf extract inhibited fluorescent AGE formation in a bovine serum albumin (BSA)-ribose system, whereas the aqueous extract had no effect in both BSA-fructose and BSA-ribose systems. The phytochemical profile was investigated with liquid chromatographyultraviolet-visible (UV-Vis) diode array coupled to electrospray ionization multistage mass spectrometry (LC/DAD/ESIMSn). Quantification of the major phenolic compounds was performed with high performance liquid chromatography with UV-Vis diode array detection and nuclear magnetic resonance spectroscopy. Among the major phenolic components (luteolin,hydroxytyrosol, luteolin-40-O-b-D-glucopyranoside, luteolin-7-O-b-D-glucopyranoside, and oleuropein), luteolin and luteolin-40-O-b-D-glucopyranoside were assigned as potent inhibitors of AGE formation. The extraction procedure greatly affects the composition and therefore the anti-glycation potential of olive leaves. KCI Citation Count: 34
ISSN:1096-620X
1557-7600
DOI:10.1094/jmf.2013.0016