Department of Anesthesiology and Intensive Care Medicine, University of Tübingen, Tübingen, Germany.
Br J Anaesth. 2012 Jun;108(6):912-21. doi: 10.1093/bja/aer518. Epub 2012 Feb 26.
Extracorporeal circulation (ECC) and hypothermia are routinely used in cardiac surgery to maintain stable circulatory parameters and to increase the ischaemic tolerance of the patient. However, ECC and hypothermia cause platelet activation and dysfunction possibly followed by a devastating coagulopathy. Stimulation of the adenosinediphosphate (ADP) receptor P(2)Y(12) plays a pivotal role in platelet activation. This experimental study tested P(2)Y(12) receptor blockade as an approach to protect platelets during ECC.
Human blood was treated with the short-acting P(2)Y(12) blocker cangrelor (1 µM, t(1/2)<5 min) or the P(2)Y(12) inhibitor 2-MeSAMP (100 µM) and circulated in an ex vivo ECC model at normothermia (37°C) and hypothermia (28°C). Before and after circulation, markers of platelet activation and of coagulation (thrombin-antithrombin complex generation) were analysed. During hypothermic ECC in pigs, the effect of reversible P(2)Y(12) blockade on platelet function was evaluated by cangrelor infusion (0.075 µg kg(-1) min(-1)).
During ex vivo hypothermic ECC, P(2)Y(12) blockade inhibited platelet granule release (P<0.01), platelet-granulocyte binding (P<0.05), and platelet loss (P<0.001), whereas no effects on platelet-ECC binding, platelet CD42bα expression, glycoprotein IIb/IIIa activation, or thrombin-antithrombin complex generation were observed. During hypothermic ECC in pigs, cangrelor inhibited platelet-fibrinogen binding (P<0.05) and ADP-induced platelet aggregation (P<0.001). Platelet function was rapidly restored after termination of cangrelor infusion.
P(2)Y(12) blockade by cangrelor prevents platelet activation during ECC and hypothermia. Owing to its short half-life, platelet inhibition can be well controlled, thus potentially reducing bleeding complications. This novel pharmacological strategy has the potential to reduce complications associated with ECC and hypothermia.
体外循环(ECC)和低温常用于心脏手术,以维持稳定的循环参数并增加患者的缺血耐受。然而,ECC 和低温会导致血小板激活和功能障碍,可能随后导致破坏性的凝血功能障碍。二磷酸腺苷(ADP)受体 P(2)Y(12)的刺激在血小板激活中起着关键作用。这项实验研究测试了 P(2)Y(12)受体阻断作为在 ECC 期间保护血小板的一种方法。
用人血处理短效 P(2)Y(12)阻滞剂坎格雷洛(1µM,t(1/2)<5 分钟)或 P(2)Y(12)抑制剂 2-MeSAMP(100µM),并在体外循环(ECC)模型中在正常体温(37°C)和低温(28°C)下循环。在循环前后,分析血小板激活和凝血(凝血酶-抗凝血酶复合物生成)的标志物。在猪的低温 ECC 中,通过坎格雷洛输注(0.075µg kg(-1)min(-1))评估可逆性 P(2)Y(12)阻断对血小板功能的影响。
在体外低温 ECC 期间,P(2)Y(12)阻断抑制血小板颗粒释放(P<0.01)、血小板-粒细胞结合(P<0.05)和血小板丢失(P<0.001),而对血小板-ECC 结合、血小板 CD42bα 表达、糖蛋白 IIb/IIIa 活化或凝血酶-抗凝血酶复合物生成没有影响。在猪的低温 ECC 中,坎格雷洛抑制血小板-纤维蛋白原结合(P<0.05)和 ADP 诱导的血小板聚集(P<0.001)。坎格雷洛输注终止后,血小板功能迅速恢复。
坎格雷洛通过 P(2)Y(12)阻断可防止 ECC 和低温期间的血小板激活。由于其半衰期短,可以很好地控制血小板抑制,从而潜在地减少出血并发症。这种新的药理学策略有可能降低与 ECC 和低温相关的并发症。