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替格瑞洛临床应用概述 被引量:7

Summary of the Clinical Application of Ticagrelor
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摘要 替格瑞洛是新型的P2Y_(12)受体抑制药,其不仅通过抑制P2Y_(12)受体途径,还通过腺苷ENT^(-1)途径发挥作用,展现了其双途径作用机制。同时其不良反应也与双途径作用机制有关。研究显示,替格瑞洛较氯吡格雷的抗血小板作用更强,使急性冠状动脉综合征患者获得较好心血管结果,并且不增加主要心血管事件和猝死率,但在亚洲临床研究尚需更多数据。 Ticagrelor is a new type of P2Y_(12) receptor inhibitor,which not only inhibits P2Y_(12) receptor pathway,but also plays a role through ENT^-1 adenosine pathway,and shows its dual mechanisms. At the same time,its adverse reactions are related to the mechanisms of double pathways. The studies have shown that ticagrelor is more resistant to platelet than clopidogrel,which results in better cardiovascular outcomes in patients with acute coronary syndrome,and does not increase major cardiovascular events and sudden death rate; however,more data are needed in Asian clinical studies.
作者 宋柳全 黎晓亮 何国欢 Song Liuquan;Li Xiaoliang;He Guohuan(Department of Pharmacy;Department of Cardiology, Wuzhou Gongren Hospital of Guangxi Province, Guangxi Wuzhou 543001, China)
出处 《中国药师》 CAS 2018年第7期1269-1274,共6页 China Pharmacist
关键词 替格瑞洛 抗血小板作用 双途经 临床应用 Ticagrelor Anti-platelet function Dual pathway mechanism Clinical application
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  • 1HaynesSE,HollopeterG,Yang G,etal.TheP2Y12receptor regulates microglial activation by extracellularnucleotides[J].NatNeurosci,2006,9(12):1512-1519. 被引量:1
  • 2DiehlP,OlivierC,HalscheidC,etal.Clopidogrelaffectsleukocyte dependent platelet aggregation by P2Y12expressingleukocytes[J].BasicResCardiol,2010,105(3):379-387. 被引量:1
  • 3AddiAB,Cammarata D,Conley PB,etal.RoleoftheP2Y12receptorinthe modulation of murinedendriticcellfunction by ADP [J].J Immunol,2010,185 (10):5900-5906. 被引量:1
  • 4KronlageM,SongJ,SorokinL,etal.Autocrinepurinergicreceptorsignalingisessentialfor macrophagechemotaxis[J].SciSignal,2010,3(132):ra55. 被引量:1
  • 5BadrnyaS,ButlerLM,SderbergNauclerC,etal.Plateletsdirectlyenhance neutrophiltransmigrationin responsetooxidisedlowdensity lipoprotein [J]. Thromb Haemost,2012,108(4):719-729. 被引量:1
  • 6WebsterCM,Hokari M,McManus A,etal.MicroglialP2Y12 deficiency/inhibition protectsagainstbrainischemia[J].PloSOne,2013,8(8):e70927. 被引量:1
  • 7JakubowskiJA,WintersKJ,Naganuma H,etal.Prasugrel:anovel thienopyridine antiplatelet agent. A review ofpreclinicalandclinicalstudiesandthemechanisticbasisforitsdistinctantiplateletprofile[J].Cardiovasc Drug Rev,2007,25(4):357-374. 被引量:1
  • 8Cannon CP,HustedS,Harrington RA,etal.Safety,tolerability,and Initial efficacy of AZD6140,the firstreversibleoraladenosinediphosphatereceptorantagonist,comparedwithclopidogrel,inpatientswithnonSTsegmentelevationacutecoronarysyndrome primaryresultsoftheDISPERSE2trial[J].J Am CollCardiol,2007,50(19):1844-1851. 被引量:1
  • 9HustedS,Emanuelsson H,HeptinstallS,etal.Pharmacodynamics,pharmacokinetics,and safety of the oralreversible P2Y12 antagonist AZD6140 with aspirin inpatientswithatherosclerosis:adoubleblindcomparisontoclopidogrelwithaspirin[J].Eur HeartJ,2006,27(9):1038-1047. 被引量:1
  • 10StoreyRF,AngiolilloDJ,PatilSB,etal.Inhibitoryeffectsofticagrelorcomparedwithclopidogrelonplateletfunctioninpatients with acute coronary syndromes: the PLATO(Plateletinhibition and patient Outcomes) PLATELETsubstudy[J].J Am Colle Cardiol, 2010, 56 (18):1456-1462. 被引量:1

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