中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Antiplatelet aggregation activity of diterpene alkaloids from Spiraea japonica

文献类型:期刊论文

作者Li, L; Shen, YM; Yang, XS; Zuo, GY; Shen, ZQ; Chen, ZH; Hao, XJ
刊名EUROPEAN JOURNAL OF PHARMACOLOGY
出版日期2002-08-02
卷号449期号:1-2页码:23-28
关键词Atisine-type Diterpene Alkaloid Platelet Aggregation Arachidonic Acid Adenosine-5 '-diphosphate Paf (Platelet-activating Factor) Structure-activity Relationship
文献子类Article
英文摘要Six diterpene alkaloids with an atisine-type C-20-skeleton isolated from the Chinese herbal medicines Spiraea japonica var. acuta and S. japonica var. ovalifolia, as well as eight derivatives of spiramine C and spiradine F were evaluated for the ability to inhibit aggregation of rabbit platelets induced by arachidonic acid, ADP, and platelet-activating factor (PAF) in vitro. The results showed that 12 of the 14 atisine-type diterpene alkaloids significantly inhibited PAF-induced platelet aggregation in a concentration-dependent manner, but had no effect on ADP- or arachidonic acid-induced aggregation, exhibiting a selective inhibition. It is the first report that C-20-diterpene alkaloids inhibit PAF-induced platelet aggregation. However, spiramine C1 concentration-dependently inhibited platelet aggregation induced by PAF, ADP and arachidonic acid with IC50 values of 30.5 +/- 2.7, 56.8 +/- 8.4 and 29.9 +/- 9.9 muM, respectively, suggesting a non-selective antiplatelet aggregation action. The inhibitory effect of spiramine C1 on arachidonic acid was as potent as that of aspirin. Primary studies of the structure-activity relationships for inhibition of PAF-induced aggregation showed that the oxygen substitution at the C-15 position and the presence of an oxazolidine ring in spiramine alkaloids were essential to their antiplatelet aggregation effects. These results suggest that the atisine-type alkaloids isolated from S. japonica are a class of novel antiplatelet aggregation agents. (C) 2002 Elsevier Science B.V All rights reserved.
学科主题Pharmacology & Pharmacy
WOS关键词PLATELET-ACTIVATING FACTOR ; WEB 2086 ; ROOTS ; ANTAGONIST ; SHOCK
WOS研究方向Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000177717600003
公开日期2012-07-25
源URL[http://ir.kib.ac.cn:8080/handle/151853/14627]  
专题昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室
作者单位1.Chinese Acad Sci, Kunming Inst Bot, Kunming 650204, Yunnan, Peoples R China
2.Kunming Med Coll, Yunnan Pharmacol Labs Nat Prod, Kunming 650031, Yunnan, Peoples R China
3.Key Lab Chem Nat Prod Guizhou Province, Guiyang 550002, Guizhou, Peoples R China
4.Chinese Acad Sci, Guiyang 550002, Guizhou, Peoples R China
推荐引用方式
GB/T 7714
Li, L,Shen, YM,Yang, XS,et al. Antiplatelet aggregation activity of diterpene alkaloids from Spiraea japonica[J]. EUROPEAN JOURNAL OF PHARMACOLOGY,2002,449(1-2):23-28.
APA Li, L.,Shen, YM.,Yang, XS.,Zuo, GY.,Shen, ZQ.,...&Hao, XJ.(2002).Antiplatelet aggregation activity of diterpene alkaloids from Spiraea japonica.EUROPEAN JOURNAL OF PHARMACOLOGY,449(1-2),23-28.
MLA Li, L,et al."Antiplatelet aggregation activity of diterpene alkaloids from Spiraea japonica".EUROPEAN JOURNAL OF PHARMACOLOGY 449.1-2(2002):23-28.

入库方式: OAI收割

来源:昆明植物研究所

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