Cyclooxygenase-2 enzyme inhibitory withanolides from Withania somnifera leaves

被引:98
作者
Jayaprakasam, B
Nair, MG [1 ]
机构
[1] Michigan State Univ, Dept Hort, E Lansing, MI 48824 USA
[2] Michigan State Univ, Natl Food Safety & Toxicol Ctr, E Lansing, MI 48824 USA
关键词
withanolides; Withania somnifera; solanaceace; antioxidant; antiinflammatory; cyclooxygenase enzyme;
D O I
10.1016/S0040-4020(02)01601-0
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Four novel withanolide glycosides and a withanolide have been isolated from the leaves of Withania somnifera. The structures of the novel compounds were elucidated as physagulin D (1-->6)-beta-D-glucopyranosyl-(1-->4)-beta-D-glucopyranoside (1), 27-O-beta-D-glucopyranosyl physagulin D (2), 27-O-beta-D-glucopyranosyl viscosalactone B (3), 4,16-dihydroxy-5beta, 6beta-epoxyphysagulin D (4), and 4-(1-hydroxy-2,2-dimethylcyclo-propanone)-2,3-dihydrowithaferin A (5) on the basis of 1D-, 2D NMR and MS spectral data. In addition, seven known withanolides withaferin A (6), 2,3-dihydrowithaferin A (7), viscosalactone B (8), 27-desoxy-24,25-dihydrowithaferin A (9), sitoindoside IX (10), physagulin D (11), and withanoside IV (12) were isolated. These withanolides were assayed to determine their ability to inhibit cycloxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) enzymes and lipid peroxidation. The withanolides tested, except compound 9, showed selective COX-2 enzyme inhibition ranging from 9 to 40% at 100 mug/ml. Compounds 4, 10 and 11 also inhibited lipid peroxidation by 40, 44 and 55%, respectively. The inhibition of COX-2 enzyme by withanolides is reported here for the first time. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:841 / 849
页数:9
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