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Cangrelor通过抑制GPR17介导的炎症缓解博来霉素诱导的小鼠肺纤维化 被引量:3
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作者 詹天玮 田雨鑫 +6 位作者 魏韬峰 董灵军 吴紫祥 王琪 张纬萍 卢韵碧 吴明 《中国药理学与毒理学杂志》 CAS CSCD 北大核心 2018年第9期739-739,共1页
目的探讨抗血小板药Cangrelor缓解博来霉素诱导的小鼠肺纤维化的作用及机制。方法整体动物实验以博来霉素(BLM)3 mg·kg-1诱导C57BL/6J小鼠发生肺纤维化,Cangrelor在给予BLM前2天至给药第14天期间给予,皮下注射,每天1次。BLM给药第1... 目的探讨抗血小板药Cangrelor缓解博来霉素诱导的小鼠肺纤维化的作用及机制。方法整体动物实验以博来霉素(BLM)3 mg·kg-1诱导C57BL/6J小鼠发生肺纤维化,Cangrelor在给予BLM前2天至给药第14天期间给予,皮下注射,每天1次。BLM给药第14天,取肺固定后石蜡切片做HE染色、Msasson′s染色和GPR17、巨噬细胞特异性免疫组化染色并做纤维化评分,Western蛋白质印迹法检测肺组织GPR17蛋白表达,定量PCR检测胶原蛋白mRNA表达、定量PCR和ELISA检测肺组织炎症因子的合成与释放。细胞实验采用RAW 264.7细胞,以博来霉素,Cangrelor和GPR17siRNA处理12 h;细胞活性以MTT法检测,以定量PCR和ELISA分别检测细胞炎症因子的合成和释放。结果 (1)BLM诱导小鼠发生肺纤维化的同时,肺组织GPR17表达和GPR17阳性巨噬细胞增加,合成和释放TNF-α,IL-6和TGF-β1增高,肺组织合成胶原Ⅰ和Ⅲ增高;Cangrelor 2.5, 5.0和10.0 mg·kg-1不仅剂量依赖性减弱BLM诱导的炎症反应和致纤维化作用,且明显减少GPR17阳性巨噬细胞的数量;(2)BLM(1 mg·L^(-1))诱导RAW 264.7巨噬细胞发生炎症的同时可促进细胞表达GPR17,抑制GPR17表达可减轻细胞炎症,Cangrelor 2.5~10.0μmol·L^(-1)浓度依赖性减轻BLM诱导的RAW264.7巨噬细胞炎症。结论 Cangrelor通过抑制GPR17介导的炎症而减轻BLM诱导的小鼠肺纤维化。 展开更多
关键词 肺纤维化 巨噬细胞 GPR17 cangrelor 炎症因子
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Effect of platelet inhibition with cangrelor during PCI on ischemic events 被引量:1
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《South China Journal of Cardiology》 CAS 2013年第1期80-81,共2页
ABSTRACT The intensity of antiplatelet therapy during percutaneous coronary intervention (PCI) is an important deter- minant of PCI-related ischemic complications. Cangrelor is a potent intravenous adenosine diphos... ABSTRACT The intensity of antiplatelet therapy during percutaneous coronary intervention (PCI) is an important deter- minant of PCI-related ischemic complications. Cangrelor is a potent intravenous adenosine diphosphate (ADP)- receptor antagonist that acts rapidly and has quickly reversible effects. 展开更多
关键词 PCI Effect of platelet inhibition with cangrelor during PCI on ischemic events
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P2Y12-ADP receptor antagonists: Days of future and past 被引量:5
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作者 Marc Laine Franck Paganelli Laurent Bonello 《World Journal of Cardiology》 CAS 2016年第5期327-332,共6页
Antiplatelet therapy is the cornerstone of the therapeutic arsenal in coronary artery disease.Thanks to a better understanding in physiology,pharmacology and pharmacogenomics huge progress were made in the field of pl... Antiplatelet therapy is the cornerstone of the therapeutic arsenal in coronary artery disease.Thanks to a better understanding in physiology,pharmacology and pharmacogenomics huge progress were made in the field of platelet reactivity inhibition thus allowing theexpansion of percutaneous coronary intervention.Stent implantation requires the combination of two antiplatelet agents acting in a synergistic way.Asprin inhibit the cyclo-oxygenase pathway of platelet activation while clopidogrel is a P2Y12 adenosine diphosphate(ADP)-receptor antagonist.This dual antiplatelet therapy has dramatically improved the prognosis of stented patients.However,due to pharmacological limitations of clopidogrel(interindividual variability in its biological efficacy,slow onset of action,mild platelet reactivity inhibition)ischemic recurrences remained high following stent implantation especially in acute coronary syndrome patients.Thus,more potent P2Y12-ADP receptor inhibitors were developped including prasugrel,ticagrelor and more recently cangrelor to overcome these pitfalls.These new agents reduced the rate of thrombotic events in acute coronary syndrome patients at the cost of an increased bleeding risk.The abundance in antiplatelet agents allow us to tailor our strategy based on the thrombotic/bleeding profile of each patient.Recently,the ACCOAST trial cast a doubt on the benefit of pre treatment in non-ST segment elevation acute coronary syndrome.The aim of the present review is to summarize the results of the main studies dealing with antiplatelet therapy in stented/acute coronary syndromes patients. 展开更多
关键词 CLOPIDOGREL PRASUGREL Ticagrelor Acute coronary syndrome Ticagrelor cangrelor
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Organ transplantation and drug eluting stents:Perioperative challenges 被引量:1
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作者 Aparna Dalal 《World Journal of Transplantation》 2016年第4期620-631,共12页
Patients listed for organ transplant frequently have severe coronary artery disease(CAD), which may be treated with drug eluting stents(DES). Everolimus and zotarolimus eluting stents are commonly used. Newer generati... Patients listed for organ transplant frequently have severe coronary artery disease(CAD), which may be treated with drug eluting stents(DES). Everolimus and zotarolimus eluting stents are commonly used. Newer generation biolimus and novolimus eluting biodegradable stents are becoming increasingly popular. Patients undergoing transplant surgery soon after the placement of DES are at increased risk of stent thrombosis(ST) in the perioperative period. Dual antiplatelet therapy(DAPT) with aspirin and a P2Y12 inhibitor such as clopidogrel, prasugrel and ticagrelor is instated post stenting to decrease the incident of ST. Cangrelor has recently been approved by Food and Drug Administration and can be used as a bridging antiplatelet drug. The risk of ischemia vs bleeding must be considered when discontinuing or continuing DAPT for surgery. Though living donor transplant surgery is an elective procedure and can be optimally timed, cadaveric organ availability is unpredictable, therefore, discontinuation of antiplatelet medication cannot be optimally timed. The type of stent and timing of transplant surgery can be of utmost importance. Many platelet function point of care tests such as Light Transmittance Aggregrometry, Thromboelastography Platelet Mapping, VerifyN ow, Multiple Electrode Aggregrometry are used to assess bleeding risk and guide perioperative platelet transfusion. Response to allogenic platelet transfusion to control severe intraoperative bleeding may differ with the antiplatelet drug. In stent thrombosis is an emergency where management with either a drug eluting balloon or a DES has shown superior outcomes. Post-transplant complications often involved stenosis of an important vessel that may need revascularization. DES are now used for endovascular interventions for transplant orthotropic heart CAD, hepatic artery stenosis post liver transplantation, transplant renal artery stenosis following kidney transplantation, etc. Several antiproliferative drugs used in the DES are inhibitors of mammalian target of rapamycin. Thus they are used for post-transplant immunosuppression to prevent acute rejection in recipients with heart, liver, lung and kidney transplantation. This article describes in detail the various perioperative challenges encountered in organ transplantation surgery and patients with drug eluting stents. 展开更多
关键词 Drug eluting STENTS cangrelor Stent thrombosis Organ transplant ANTIPLATELET medication PLATELET function assays Mammalian target of rapamycin inhibitors POST-TRANSPLANT immunosuppression POST-TRANSPLANT ENDOVASCULAR inhibition Ticagrelor Thromboelastograms PLATELET mapping Novolimus Biolimus A9
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二磷酸腺苷受体拮抗剂类抗血小板药物研究进展 被引量:9
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作者 吴雅凝 赵娣 +1 位作者 李宁 陈西敬 《中国临床药理学与治疗学》 CAS CSCD 2010年第12期1434-1440,共7页
抗血小板治疗对急性冠脉综合症和预防经皮冠脉介入手术患者形成血栓的效果很好,可以显著降低上述两种疾病的致死率和发病率。目前最常用的药物是阿司匹林与氯吡格雷,但是一些临床数据表明,这两种药物的合用并不是对所有的病人都有很好... 抗血小板治疗对急性冠脉综合症和预防经皮冠脉介入手术患者形成血栓的效果很好,可以显著降低上述两种疾病的致死率和发病率。目前最常用的药物是阿司匹林与氯吡格雷,但是一些临床数据表明,这两种药物的合用并不是对所有的病人都有很好的疗效,这可能会造成一些心血管方面的不良反应。所以,对一些有前途的、新的抗血小板药物进行进一步的研究就显得十分有必要。本文对二磷酸腺苷受体拮抗剂类抗血小板药物(如氯吡格雷、普拉格雷、替卡格雷、坎格雷洛等)的代谢和作用特点进行综述,为临床用药提供参考。 展开更多
关键词 抗血小板药物 P2Y12受体 普拉格雷 替卡格雷 坎格雷洛
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Medcines公司的一种抗血栓药物
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作者 王吉云 《国外药讯》 2004年第4期12-12,共1页
关键词 Medcines公司 抗血栓药物 cangrelor 血栓形成 血小板功能
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新型抗血小板药坎格瑞洛的国外研究现状 被引量:3
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作者 丁琮洋 孟璐 +5 位作者 王小楠 付冉 范理菊 崔艳军 李亚静 董占军 《实用药物与临床》 CAS 2021年第3期280-284,共5页
新型抗血小板药物坎格瑞洛是首个速效、静脉使用的抗血小板药物,可逆性地与P2Y12受体结合,发挥抗血小板作用,与传统的抗血小板药物氯吡格雷相比,其起效迅速、半衰期短,已广泛应用于需要进行冠脉介入治疗(PCI)的急性冠脉综合征(ACS)患者... 新型抗血小板药物坎格瑞洛是首个速效、静脉使用的抗血小板药物,可逆性地与P2Y12受体结合,发挥抗血小板作用,与传统的抗血小板药物氯吡格雷相比,其起效迅速、半衰期短,已广泛应用于需要进行冠脉介入治疗(PCI)的急性冠脉综合征(ACS)患者和心源性休克患者中。CHAMPION试验以患者死亡、心肌梗死和心肌缺血导致的血管重建作为观察终点,证实了坎格瑞洛的治疗作用。坎格瑞洛应用在原位心脏移植、发绀型先天性心脏病及肝素诱导血小板减少症(HIT)的治疗中,都展现了一定的优势。桥接疗法和过渡疗法使用坎格瑞洛与口服P2Y12受体抑制剂,在外科手术抗血小板和减少不良事件中发挥了重要作用。 展开更多
关键词 坎格瑞洛 急性冠脉综合征 心源性休克 桥接疗法 过渡疗法
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坎格瑞洛和氯吡格雷治疗冠心病患者疗效和安全性的Meta分析 被引量:1
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作者 杨幼生 卓朝贵 +1 位作者 童随阳 王欣 《疑难病杂志》 CAS 2014年第11期1176-1181,共6页
目的比较坎格瑞洛与氯毗格雷治疗冠心病的疗效和安全性。方法计算机检索PubMed、MED—LINE、CochraneCentralRegisterofControlledTrials、中国生物医学文献数据库、CNKI全文数据库,收集2001年1月-2014年6月公开发表的有关坎格瑞洛和... 目的比较坎格瑞洛与氯毗格雷治疗冠心病的疗效和安全性。方法计算机检索PubMed、MED—LINE、CochraneCentralRegisterofControlledTrials、中国生物医学文献数据库、CNKI全文数据库,收集2001年1月-2014年6月公开发表的有关坎格瑞洛和氯吡格雷疗效比较的随机对照试验(RCT),手检已获文献的参考文献、会议摘要及相关网站。对文献质量进行严格评价后,对符合要求的RCT进行资料提取并采用RevMan5.0软件进行Meta分析。结果共纳入4项RCT,计38227例。Meta分析显示:坎格瑞洛组与氯吡格雷组之间全因死亡率(OR=0.80,95%C10.62~1.03,P=0.08)、心肌梗死(MI)发生率(OR=0.92,95%C10.80—1.06,P=0.27)、主要不良心脏事件(MACE)发生率(OR=0.83,95%C10.67~1.03,P=0.09)、大出血发生率(OR=1.00,95%C10.68~1.47,P=0.99),脑卒中发生率(OR=1.17,95%C10.61~2.24,P:0.63)均无统计学意义;坎格瑞洛组支架内血栓发生率(OR=0.62,95%C10.48—0.80,P=0.0002)低于氯吡格雷组。结论坎格瑞洛能显著降低支架内血栓发生率,在全因死亡率、MI发生率、MACE发生率、大出血发生率、脑卒中发生率与氯吡格雷相似,初步显示了坎格瑞洛疗效的优越性。 展开更多
关键词 坎格瑞洛 氯吡格雷 冠心病 META分析
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坎格雷洛的合成工艺改进
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作者 林汉轩 王素云 王立峰 《中国医药工业杂志》 CAS CSCD 北大核心 2020年第8期987-991,共5页
本研究对坎格雷洛(1)的合成工艺进行了改进。鸟嘌呤核苷(2)经乙酰化反应、2步氯代反应得2,6-二氯-9-(2,3,5-三-O-乙酰基-β-D-呋喃核糖基)嘌呤(5),5经氨基取代、脱保护和硫代反应得N6-(2-甲硫基乙基)-2-(3,3,3-三氟丙硫基)腺嘌呤核苷(8... 本研究对坎格雷洛(1)的合成工艺进行了改进。鸟嘌呤核苷(2)经乙酰化反应、2步氯代反应得2,6-二氯-9-(2,3,5-三-O-乙酰基-β-D-呋喃核糖基)嘌呤(5),5经氨基取代、脱保护和硫代反应得N6-(2-甲硫基乙基)-2-(3,3,3-三氟丙硫基)腺嘌呤核苷(8)。硫代反应中,采用自制的三氟丙硫醇代替过硫醚试剂,提高了反应活性,6步总收率由15%提高至33%。由8合成1时,使用“一锅法”3步连续反应,并且后处理时采用正丁醇萃取纯化代替离子交换分离纯化,操作简便,产物1纯度达到99.10%。 展开更多
关键词 坎格雷洛 抗凝血药 合成 工艺改进
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GPR17 modulates anxiety-like behaviors via basolateral amygdala to ventral hippocampal CA1 glutamatergic projection 被引量:1
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作者 Ruizhe Nie Xinting Zhou +9 位作者 Jiaru Fu Shanshan Hu Qilu Zhang Weikai Jiang Yizi Yan Xian Cao Danhua Yuan Yan Long Hao Hong Susu Tang 《Acta Pharmaceutica Sinica B》 SCIE CAS CSCD 2024年第11期4789-4805,共17页
Anxiety disorders are one of the most epidemic and chronic psychiatric disorders.An incom-plete understanding of anxiety pathophysiology has limited the development of highly effective drugs against these disorders.GP... Anxiety disorders are one of the most epidemic and chronic psychiatric disorders.An incom-plete understanding of anxiety pathophysiology has limited the development of highly effective drugs against these disorders.GPR17 has been shown to be involved in multiple sclerosis and some acute brain injury disorders.However,no study has investigated the role of GPR17 in psychiatric disorders.In a well-established chronic restraint stress(CRS)mouse model,using a combination of pharmacological and molecular biology techniques,viral tracing,in vitro electrophysiology recordings,in vivo fiber photom-etry,chemogenetic manipulations and behavioral tests,we demonstrated that CRS induced anxiety-like behaviors and increased the expression of GPR17 in basolateral amygdala(BLA)glutamatergic neurons.Inhibition of GPR17 by cangrelor or knockdown of GPR17 by adeno-associated virus in BLA glutama-tergic neurons effectively improved anxiety-like behaviors.Overexpression of GPR17 in BLA glutama-tergic neurons increased the susceptibility to anxiety-like behaviors.What's more,BLA glutamatergic neuronal activity was required for anxiolytic-like effects of GPR17 antagonist and GPR17 modulated anxiety-like behaviors via BLA to ventral hippocampal CAl glutamatergic projection.Our study finds for the first and highlights the new role of GPR17 in regulating anxiety-like behaviors and it might be a novel potential target for therapy of anxiety disorders. 展开更多
关键词 GPR17 CRS Anxiety Basolateral amygdala VentralhippocampalCAl Glutamatergic neurons Glutamatergic projection cangrelor
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