首都医科大学学报 ›› 1991, Vol. 12 ›› Issue (3): 171-179.

• 论著 • 上一篇    下一篇

血栓素B2的高效液相荧光测定及刺五加提取物的抗血小板作用

杨秋生1, 金有豫1, 王津生2   

  1. 1. 首都医学院药理学教研室;2. 中国肉类食品研究中心
  • 收稿日期:1990-01-18 修回日期:1900-01-01 出版日期:1991-07-15 发布日期:1991-07-15

HPLC Analysis of TXB2 Content in Platelet and the Anti-platelet Actions of Acathopanax Senticosus

Yang Qiushen1, Jin Youyu1, Wang Jinsheng2   

  1. 1. Department of Pharmacology, Capital Institute of Medicine;2. China Meat Research Center
  • Received:1990-01-18 Revised:1900-01-01 Online:1991-07-15 Published:1991-07-15

摘要: 本文在Turk及Wintersteiger荧光衍生实验的基础上,建立了反相HPLC法测定血小板TXB2含量的方法.血小板TXB2用Sep-PakC18提取,在冠醚和碳酸钾存在下,BrMmc与TXB2的羧基反应生成BrMmc-TXB2。然后经Zorbax-ODS柱(250mm×4.6mm,5μm)分离,测定荧光强度(E×345,Em405)。流动相为乙腈:水:磷酸(60:40:0.1V/V),流速1ml/min.BrMmc-TXB2的分离在20min内完成。TXB2的含量用外标法定量,检测限15ng。体外实验刺五加提取物(0.275~2.2mg/mlPRP)对AA、ADP诱导的家兔血小板聚集有明显的抑制作用,并能抑制AA诱导的血小板TXB2的生成。静脉注射(120mg/kg)对AA、ADP诱导的聚集也有抑制作用。

关键词: 反相HPLC, 血栓素B2, 血小板

Abstract: TXB2 content in platelet were analysed by high-performance liquid chromatography (HPLC) using a pre-column derivatization method,in which a fluorescentreagent,4-bro-momethyl-7-methoxycoumarin (BrMmc) was used.The mothod was applied to studing the effects of Acanthopanax Senticosus (A.S.) extract,a Chinese medicine,on platelet func-tion.The platelet TXB2 were extracted by a Sep-Pak C18 (waters).In the presence of 18-crown-6 and K2CO3,BrMmc reacted with carboxylic group(—COOH) of TXB2 to form a fluorescent ester (BrMmc-TXB2),which was seperated on a column (250mm×4.6mm I.D.)packed with Zorbax-ODS (6 μm,Dupont Instruments)and monitored by a fluorescent detector in Ex 345 nm and Em 405 nm.The mobile phase (acetonitrile:water:phosphoric acid;60:40:0.1 V/V),flowed at 1 ml/min at 30℃.The seperation of BrMmc-TXB2 was completed in 20min.The detection limit was 15 ng using the external standard method.The anti-platelet actions of A.S.in rabbit were studied.The resultes (in vitro) showed that the platelet aggregations induced by AA and ADP were potently inhibited by A.S.in a dose-de-pendent manner and the AA-induced TXB2 formation in platelet was also reduced.After in-travenous injection of A.S.(120mg/kg),the platelet aggregations induced by AA and ADP were inhibited and the effects lasted 30 and 45 min,respectively.

Key words: RP-HPLC, TXB2, platelet