王峰, 刘敏, 杨连春, 王京媛, 吕敏, 李菲. 新的非肽类内皮素拮抗剂:咖啡酸、阿魏酸J. 药学学报, 1999, 34(12): 898-901.
引用本文: 王峰, 刘敏, 杨连春, 王京媛, 吕敏, 李菲. 新的非肽类内皮素拮抗剂:咖啡酸、阿魏酸J. 药学学报, 1999, 34(12): 898-901.
Wang Feng, Liu Min Yang Lianchun, Wang Jingyuan Lü Min , Li Fei, . A NEW KIND OF NON PEPTIDE ENDOTHELIN ANTAGONISTS: CAFFEIC ACID AND FERULIC ACIDJ. Acta Pharmaceutica Sinica, 1999, 34(12): 898-901.
Citation: Wang Feng, Liu Min Yang Lianchun, Wang Jingyuan Lü Min , Li Fei, . A NEW KIND OF NON PEPTIDE ENDOTHELIN ANTAGONISTS: CAFFEIC ACID AND FERULIC ACIDJ. Acta Pharmaceutica Sinica, 1999, 34(12): 898-901.

新的非肽类内皮素拮抗剂:咖啡酸、阿魏酸

A NEW KIND OF NON PEPTIDE ENDOTHELIN ANTAGONISTS: CAFFEIC ACID AND FERULIC ACID

  • 摘要: 目的:研究桂皮酸类化合物咖啡酸和阿魏酸对内皮素(endothelin1,ET-1) 生物效应的拮抗作用。方法:体内ET1iv 致小鼠急性死亡、体外血管平滑肌细胞培养、主动脉条收缩试验和ET 受体结合试验。结果:咖啡酸和阿魏酸(ip) 能剂量依赖性地显著延长ET-1 致小鼠急性死亡时间,在离体器官可观察到咖啡酸与阿魏酸能拮抗ET-1的缩血管效应;放射性受体配体结合实验表明,咖啡酸和阿魏酸可竞争性地抑制ET-1 与其受体的结合。结论:咖啡酸和阿魏酸为新的非肽类ET 拮抗剂。

     

    Abstract: AIM: To evaluate the effects of caffeic acid and ferulic acid on the biological responses induced by endothelin -1(ET-1) and study the mechanism of their antagonistic actions on endothelin-1. METHODS: Acute death of mouse induced by iv ET-1, isolated artery ring constrictions and rabbit aortic vascular smooth cells (RAVSMC) proliferation induced by ET-1 were used to observe the antagonistic effects of caffeic acid and ferulic acid on ET-1. Also, the 125I-ET-1 binding with 3T3 cells were employed to measure the effects of caffeic acid and ferulic acid on binding potency. RESULTS: Caffeic acid and ferulic acid were shown to increase the mouse survival time induced by ET-1 iv administration and decrease the vasoconstrictions of isolated aortic rings. Both acids were found to bind competitively with 125I-ET-1 on 3T3 cells. CONCLUSION: Caffeic acid and ferulic acid are a new kind of non peptide endothelin antagonists.

     

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