陈文梅, 金鸣, 吴伟, 李金荣, 臧宝霞, 朴永哲. 红花黄酮成分抑制血小板激活因子介导的血小板活化作用J. 药学学报, 2001, 36(12): 881-885.
引用本文: 陈文梅, 金鸣, 吴伟, 李金荣, 臧宝霞, 朴永哲. 红花黄酮成分抑制血小板激活因子介导的血小板活化作用J. 药学学报, 2001, 36(12): 881-885.
CHEN Wen-mei, JIN Ming, WU Wei, LI Jin-rong, ZANG Bao-xia, PIAO Yong-zhe. INHIBITORY EFFECT OF FLAVONOLS OF CARTHAMUS TINCTORIUS L. AGAINST RABBIT PLATELET ACTIVATION INDUCED BY PLATELET ACTIVATING FACTORJ. Acta Pharmaceutica Sinica, 2001, 36(12): 881-885.
Citation: CHEN Wen-mei, JIN Ming, WU Wei, LI Jin-rong, ZANG Bao-xia, PIAO Yong-zhe. INHIBITORY EFFECT OF FLAVONOLS OF CARTHAMUS TINCTORIUS L. AGAINST RABBIT PLATELET ACTIVATION INDUCED BY PLATELET ACTIVATING FACTORJ. Acta Pharmaceutica Sinica, 2001, 36(12): 881-885.

红花黄酮成分抑制血小板激活因子介导的血小板活化作用

INHIBITORY EFFECT OF FLAVONOLS OF CARTHAMUS TINCTORIUS L. AGAINST RABBIT PLATELET ACTIVATION INDUCED BY PLATELET ACTIVATING FACTOR

  • 摘要: 目的 观察红花黄酮成分杨梅素(Myr)和山奈酚(Kae)对血小板激活因子(PAF)诱导的兔洗涤血小板聚集、5 HT释放及血小板内游离钙离子浓度升高的影响。方法 以比浊法测定家兔洗涤血小板(WRP)聚集,邻苯二甲醛(OPT)荧光法测定5-HT浓度,Fura-2荧光探针测定血小板内游离钙离子浓度。结果 Myr和Kae体外呈浓度依赖性地抑制PAF诱发的WRP聚集及5-HT释放。Myr抑制WRP聚集的IC50 为17.5 μmol·L-1 ;抑制5-HT释放的IC50 为64.1μmol·L-1 。Kae抑制聚集、释放作用的IC50 分别为73.7μmol·L-1 和128μmol·L-1 ;同时Myr和Kae均能明显抑制PAF引起的血小板内游离钙增高。结论 Myr和Kae可抑制PAF诱导的血小板活化作用

     

    Abstract: AIM To observe the inhibitory effect of myricetin (Myr) and kaempferol (Kae) (components of Carthamus tinctorius L.) against washed rabbit platelet (WRP) aggregation, 5-HT release and intercellular free calcium concentration elevation induced by platelet activating factor (PAF). METHODS The platelet aggregation induced by PAF was determined with turbidity assay. The platelet 5-HT release and platelet inner free calcium concentration elevation induced by PAF were measured by OPT fluorescence assay and Fura-2/AM probe fluorescent technique respectively. RESULTS The WRP aggregation and 5-HT release induced by PAF (9.55×10-9mol·L-1) were both inhibited by Myr and Kae in a concentration dependent manner. WRP aggregation rate can be significantly decreased by Myr and Kae. Low concentration Kae (21.8 μmol·L-1) showed no inhibition effect against platelet aggregation. The IC50 of Myr and Kae against WRP aggregation were 17.5 μmol·L-1 and 73.7 μmol·L-1 respectively. It was shown by OPT fluorescence assay that Myr (7.86 μmol·L-1) and Kae (21.8 μmol·L-1) were not effective against platelet 5 HT release (P>0.05). The IC50 of Myr was 64.1 μmol·L-1 and that of Kae was 128 μmol·L-1. It was also found that the platelet inner free calcium concentration elevation evoked by PAF (4.78×10-10mol·L-1) was inhibited by Myr and Kae. CONCLUSION The rabbit platelet activation induced by platelet activating factor can be inhibited by Myr and Kae.

     

/

返回文章
返回