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氯吡格雷在体外对二磷酸腺苷诱导的血小板聚集有特异性抑制作用。

Specific inhibition of ADP-induced platelet aggregation by clopidogrel in vitro.

作者信息

Weber A A, Reimann S, Schrör K

机构信息

Institut für Pharmakologie, Heinrich-Heine-Universität Düsseldorf, Germany.

出版信息

Br J Pharmacol. 1999 Jan;126(2):415-20. doi: 10.1038/sj.bjp.0702276.

Abstract
  1. The thienopyridine clopidogrel is a specific inhibitor of ADP-induced platelet aggregation ex vivo. No direct effects of clopidogrel (< or = 100 microM) on platelet aggregation in vitro have been described so far. 2. Possible in vitro antiaggregatory effects (turbidimetry) of clopidogrel were studied in human platelet-rich plasma and in washed platelets. 3. Incubation of platelet-rich plasma with clopidogrel (< or = 100 microM) for up to 8 h did not result in any inhibition of ADP (6 microM)-induced platelet aggregation. 4. Incubation of washed platelets with clopidogrel resulted in a time- (maximum effects after 30 min) and concentration-dependent (IC50 1.9+/-0.3 microM) inhibition of ADP (6 microM)-induced platelet aggregation. Clopidogrel (30 microM) did not inhibit collagen (2.5 microg ml(-1))-, U46619 (1 microM)- or thrombin (0.1 u ml(-1))-induced platelet aggregation. The inhibition of ADP-induced aggregation by clopidogrel (30 microM) was insurmountable indicating a non-equilibrium antagonism of ADP actions. The R enantiomer SR 25989 C (30 microM) was significantly less active than clopidogrel (30 microM) in inhibiting platelet aggregation (32+/-5% vs 70+/-1% inhibition, P < 0.05, n = 5). 5. In washed platelets, clopidogrel (< or = 30 microM) did not significantly reverse the inhibition of prostaglandin E1 (1 microM)-induced platelet cyclic AMP formation by ADP (6 microM). 6. The antiaggregatory effects of clopidogrel were unchanged when the compound was removed from the platelet suspension. However, platelet inhibition by clopidogrel was completely abolished when albumin (350 mg ml(-1)) was present in the test buffer. 7. It is concluded that clopidogrel specifically inhibits ADP-induced aggregation of washed platelets in vitro without hepatic bioactivation. Inhibition of ADP-induced platelet aggregation by clopidogrel in vitro occurs in the absence of measurable effects on the reversal of PGE1-stimulated cyclic AMP by ADP.
摘要
  1. 噻吩并吡啶类药物氯吡格雷是体外ADP诱导的血小板聚集的特异性抑制剂。目前尚未发现氯吡格雷(≤100微摩尔)对体外血小板聚集有直接作用。2. 在富含人血小板的血浆和洗涤后的血小板中研究了氯吡格雷可能的体外抗聚集作用(比浊法)。3. 用氯吡格雷(≤100微摩尔)孵育富含血小板的血浆长达8小时,并未导致对ADP(6微摩尔)诱导的血小板聚集产生任何抑制作用。4. 用氯吡格雷孵育洗涤后的血小板导致对ADP(6微摩尔)诱导的血小板聚集产生时间依赖性(30分钟后达到最大效应)和浓度依赖性(IC50为1.9±0.3微摩尔)抑制作用。氯吡格雷(30微摩尔)不抑制胶原(2.5微克/毫升)、U46619(1微摩尔)或凝血酶(0.1单位/毫升)诱导的血小板聚集。氯吡格雷(30微摩尔)对ADP诱导的聚集的抑制作用是不可克服的,表明对ADP作用存在非平衡拮抗。R对映体SR 25989 C(30微摩尔)在抑制血小板聚集方面的活性明显低于氯吡格雷(30微摩尔)(抑制率分别为32±5%和70±1%,P<0.05,n = 5)。5. 在洗涤后的血小板中,氯吡格雷(≤30微摩尔)并未显著逆转ADP(6微摩尔)对前列腺素E1(1微摩尔)诱导的血小板环磷酸腺苷形成的抑制作用。6. 当从血小板悬液中去除该化合物时,氯吡格雷的抗聚集作用不变。然而,当测试缓冲液中存在白蛋白(350毫克/毫升)时,氯吡格雷对血小板的抑制作用完全消失。7. 得出结论,氯吡格雷在体外特异性抑制洗涤后的血小板的ADP诱导聚集,无需肝脏生物活化。氯吡格雷在体外对ADP诱导的血小板聚集的抑制作用在对ADP逆转PGE1刺激的环磷酸腺苷无明显可测作用的情况下发生。

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