Nylander Sven, Schulz Rainer
AstraZeneca R&D, Mölndal, Sweden.
Institute of Physiology, Justus-Liebig University Giessen, Giessen, Germany.
Br J Pharmacol. 2016 Apr;173(7):1163-78. doi: 10.1111/bph.13429. Epub 2016 Feb 24.
The effect and clinical benefit of P2Y12 receptor antagonists may not be limited to platelet inhibition and the prevention of arterial thrombus formation. Potential additional effects include reduction of the pro-inflammatory role of activated platelets and effects related to P2Y12 receptor inhibition on other cells apart from platelets. P2Y12 receptor antagonists, thienopyridines and ticagrelor, differ in their mode of action being prodrugs instead of direct acting and irreversibly instead of reversibly binding to P2Y12 . These key differences may provide different potential when it comes to additional effects. In addition to P2Y12 receptor blockade, ticagrelor is unique in having the only well-documented additional target of inhibition, the equilibrative nucleoside transporter 1. The current review will address the effects of P2Y12 receptor antagonists beyond platelets and the protection against arterial thrombosis. The discussion will include the potential for thienopyridines and ticagrelor to mediate anti-inflammatory effects, to conserve vascular function, to affect atherosclerosis, to provide cardioprotection and to induce dyspnea.
P2Y12受体拮抗剂的作用效果和临床益处可能不限于抑制血小板和预防动脉血栓形成。潜在的额外作用包括减轻活化血小板的促炎作用,以及P2Y12受体抑制对除血小板外其他细胞的相关作用。P2Y12受体拮抗剂、噻吩并吡啶类药物和替格瑞洛的作用方式不同,前者是前体药物而非直接作用药物,与P2Y12受体的结合是不可逆的而非可逆的。在涉及额外作用时,这些关键差异可能带来不同的可能性。除了阻断P2Y12受体外,替格瑞洛的独特之处在于它是唯一有充分文献记载的具有额外抑制靶点的药物,即平衡核苷转运体1。本综述将阐述P2Y12受体拮抗剂在血小板之外的作用以及对动脉血栓形成的保护作用。讨论内容将包括噻吩并吡啶类药物和替格瑞洛介导抗炎作用、维持血管功能、影响动脉粥样硬化、提供心脏保护以及诱发呼吸困难的可能性。