Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/62122
標題: Antioxidant and Anti-Inflammatory Effects of Orthosiphon aristatus and Its Bioactive Compounds
作者: Hsu, C.L.
顏國欽
Hong, B.H.
Yu, Y.S.
Yen, G.C.
關鍵字: Orthosiphon aristatus;antioxidant activity;anti-inflammation;RAW;264.7 cells;ursolic acid;nitric-oxide synthase;medicinal-plants;constituents;inhibition;expression;flavonoids;progress;leaves;foods;assay
Project: Journal of Agricultural and Food Chemistry
期刊/報告no:: Journal of Agricultural and Food Chemistry, Volume 58, Issue 4, Page(s) 2150-2156.
摘要: 
Orthosiphon aristatus (Blume) Miq., which can be used as a food ingredient, is grown throughout Southeast Asia and Australia. O. aristatus is frequently used for the treatment of renal inflammation, kidney stones and dysuria. The focus of the current work was to study the antioxidant and anti-inflammatory effects of methanol, ethanol and water extracts from O. aristatus (abbreviated as MEOA, EEOA and WEOA, respectively). The evaluation of antioxidant activity was determined by total phenolics, Trolox equivalent antioxidant capacity (TEAC), oxygen-radical absorbance capacity (ORAC) and cellular antioxidant activity (CAA) assays. These assays demonstrated a relatively high antioxidant activity for MEOA and EEOA. These results revealed that EEOA had the most prominent inhibitory effect on lipopolysaccharide (LPS)-stimulated nitric oxide (NO), prostaglandin E(2) (PGE(2)) and intracellular reactive oxygen species (ROS) production in RAW 264.7 cells. A high performance liquid chromatography profile indicated that MEOA and EEOA contained both ursolic acid and oleanolic acid. Moreover, ursolic acid significantly reduced NO production in LPS-stimulated RAW 264.7 cells. Both EEOA and ursolic acid inhibited LPS-stimulated protein and mRNA expression of both inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in these cells. These results demonstrate that EEOA and its bioactive compound, ursolic acid, suppress LPS-induced NO and PGE(2) production by inhibiting ROS generation, along with reducing expression of iNOS and COX-2 in RAW 264.7 cells.
URI: http://hdl.handle.net/11455/62122
ISSN: 0021-8561
DOI: 10.1021/jf903557c
Appears in Collections:食品暨應用生物科技學系

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