Department of Pharmacology, University of Michigan, Ann Arbor, MI, USA.
Department of Pharmacology, University of Michigan, Ann Arbor, MI, USA; Department of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI, USA.
Trends Pharmacol Sci. 2017 Nov;38(11):1006-1015. doi: 10.1016/j.tips.2017.08.001. Epub 2017 Aug 29.
Platelets are key contributors to the formation of occlusive thrombi; the major underlying cause of ischemic heart disease and stroke. Antiplatelet therapy has reduced the morbidity and mortality associated with thrombotic events; however, the utility of current antiplatelet therapies is limited by the concomitant risk of an adverse bleeding event. Novel antiplatelet therapies that are more efficacious at inhibiting thrombosis while minimally affecting hemostasis are required. Platelet-type 12-(S)-lipoxygenase (12-LOX), an oxygenase shown to potentiate platelet activation, represents a novel antiplatelet target. Recently, a selective 12-LOX inhibitor, ML355, was shown to decrease thrombosis without prolonging hemostasis. While published data suggests targeting 12-LOX is a viable approach, further work is required to determine the safety and effectiveness of 12-LOX inhibitors in humans.
血小板是形成闭塞性血栓的主要贡献者;是缺血性心脏病和中风的主要潜在原因。抗血小板治疗降低了与血栓事件相关的发病率和死亡率;然而,当前抗血小板治疗的效用受到伴随的不良出血事件风险的限制。需要新型的抗血小板治疗,这些治疗在最小程度上影响止血的情况下更有效地抑制血栓形成。血小板型 12-(S)-脂氧合酶(12-LOX)是一种增强血小板激活的氧合酶,代表了一种新型的抗血小板靶点。最近,一种选择性的 12-LOX 抑制剂 ML355 被证明可以减少血栓形成而不延长止血时间。虽然已发表的数据表明靶向 12-LOX 是一种可行的方法,但仍需要进一步的工作来确定 12-LOX 抑制剂在人体中的安全性和有效性。