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作 者:许长林[1] 单璐琛[1] 孙业伟[1] 王玉强[1]
出 处:《中药材》2010年第9期1450-1453,共4页Journal of Chinese Medicinal Materials
摘 要:目的:观察川芎嗪衍生物TBN体内、外对家兔血小板聚集的影响,并与其母核结构川芎嗪(TMP)相比较。方法:利用二磷酸腺苷(ADP)、血小板活化因子(PAF)及花生四烯酸(AA)诱导家兔血小板聚集,采用Born氏比浊法,测定5 min血小板最大聚集率。观察给予TBN后血小板聚集率的变化,并与TMP相比较。结果:川芎嗪衍生物TBN体内、外均能显著降低由ADP、PAF及AA诱导的5 min血小板最大聚集率,作用强于其母核结构川芎嗪;体内作用与阿司匹林相当。结论:川芎嗪衍生物TBN具有较强的抗ADP、PAF及AA诱导的血小板聚集作用,其作用强于其母核结构川芎嗪。Objective: To investigate the inhibitory effect of TBN on rabbit platelet aggregation in vitro and in vivo,and cimpare with tetramethylpyrazine(TMP).Methods:To seek out the maximum of platelet aggregation(expressed in percentage) within 5 minutes which was induced by ADP,PAF and AA according to the Born turbidimetric method with a Platelet-Aggregometer.Results:TBN significantly inhibited platelet aggregation induced by ADP,PAF and AA both in vitro and in vivo.TBN was more active than TMP.Conclusion:TBN has significant activity inhibiting platelet aggregation induced by ADP,PAF and AA in vitro and in vivo.
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