Department of Internal Medicine, Division of Hematology/Oncology, University of Iowa, Iowa City, IA, USA.
Cardiovasc Res. 2023 Nov 25;119(15):2497-2507. doi: 10.1093/cvr/cvad149.
Current antithrombotic therapies used in clinical settings target either the coagulation pathways or platelet activation receptors (P2Y12 or GPIIb/IIIa), as well as the cyclooxygenase (COX) enzyme through aspirin. However, they are associated with bleeding risk and are not suitable for long-term use. Thus, novel strategies which provide broad protection against platelet activation with minimal bleeding risks are required. Regardless of the nature of agonist stimulation, platelet activation is an energy-intensive and ATP-driven process characterized by metabolic switching toward a high rate of aerobic glycolysis, relative to oxidative phosphorylation (OXPHOS). Consequently, there has been considerable interest in recent years in investigating whether targeting metabolic pathways in platelets, especially aerobic glycolysis and OXPHOS, can modulate their activation, thereby preventing thrombosis. This review briefly discusses the choices of metabolic substrates available to platelets that drive their metabolic flexibility. We have comprehensively elucidated the relevance of aerobic glycolysis in facilitating platelet activation and the underlying molecular mechanisms that trigger this switch from OXPHOS. We have provided a detailed account of the antiplatelet effects of targeting vital metabolic checkpoints such as pyruvate dehydrogenase kinases (PDKs) and pyruvate kinase M2 (PKM2) that preferentially drive the pyruvate flux to aerobic glycolysis. Furthermore, we discuss the role of fatty acids and glutamine oxidation in mitochondria and their subsequent role in driving OXPHOS and platelet activation. While the approach of targeting metabolic regulatory mechanisms in platelets to prevent their activation is still in a nascent stage, accumulating evidence highlights its beneficial effects as a potentially novel antithrombotic strategy.
目前临床应用的抗栓治疗方法主要针对凝血途径或血小板激活受体(P2Y12 或 GPIIb/IIIa),以及通过阿司匹林抑制环氧化酶(COX)。然而,这些方法都与出血风险相关,并不适合长期使用。因此,需要寻找新的策略,以最小的出血风险提供广泛的血小板激活保护。无论激动剂刺激的性质如何,血小板激活都是一个能量密集型和 ATP 驱动的过程,其特征是代谢向有氧糖酵解的高速率切换,相对于氧化磷酸化(OXPHOS)。因此,近年来人们对靶向血小板代谢途径,特别是有氧糖酵解和 OXPHOS,以调节其激活从而预防血栓形成的方法产生了浓厚的兴趣。
本综述简要讨论了可驱动血小板代谢灵活性的代谢底物的选择。我们全面阐明了有氧糖酵解在促进血小板激活中的作用以及触发这种从 OXPHOS 转变的潜在分子机制。我们详细描述了靶向关键代谢检查点(如丙酮酸脱氢酶激酶(PDKs)和丙酮酸激酶 M2(PKM2))以抑制糖酵解的抗血小板作用。此外,我们还讨论了脂肪酸和谷氨酰胺在线粒体中的氧化作用及其在驱动 OXPHOS 和血小板激活中的后续作用。
虽然靶向血小板代谢调节机制以防止其激活的方法仍处于起步阶段,但越来越多的证据强调了它作为一种潜在的新型抗血栓形成策略的有益效果。