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首页> 外文期刊>Fundamental & clinical pharmacology. >Interactions between aspirin and COX-2 inhibitors or NSAIDs in a rat thrombosis model.
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Interactions between aspirin and COX-2 inhibitors or NSAIDs in a rat thrombosis model.

机译:阿司匹林与COX-2抑制剂或NSAID在大鼠血栓形成模型中的相互作用。

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摘要

Abstract Recent in vitro studies, clinical trials and epidemiological studies have suggested possible interactions between aspirin and other cyclo-oxygenase (COX) inhibitors, such as ibuprofen of the COX-2 inhibitors celecoxib and rofecoxib. The objective of this study was to test the effects of aspirin (1, 2.5 and 5 mg/kg), and ibuprofen (4 and 15 mg/kg), diclofenac (2.5 mg/kg), flurbiprofen (2 mg/kg), celecoxib (7.5 mg/kg), and rofecoxib (1 mg/kg), alone or combined on a rat model of arterial thrombosis. Drugs were given orally daily for 7 days, before insertion of an arterio-venous shunt thrombosis system, left in place for 15 min. Main parameter was thrombus weight. Five to 12 rats were used per experiment, and 35 controls overall. Aspirin inhibited thrombus formation in a dose-dependent manner. All NSAIDS given alone also inhibited thrombus formation to approximately the same level as aspirin 1 mg/kg/day. Ibuprofen, celecoxib and rofecoxib inhibited the effects of aspirin, but not diclofenac or flurbiprofen. The interactions with aspirin do not seem to affect all NSAIDs to equal levels. The clinical impact of this needs to be confirmed in adequately powered clinical trials or pharmaco-epidemiological studies.
机译:摘要最近的体外研究,临床试验和流行病学研究表明,阿司匹林与其他环加氧酶(COX)抑制剂之间可能存在相互作用,例如COX-2抑制剂塞洛昔布和罗非考昔的布洛芬。这项研究的目的是测试阿司匹林(1、2.5和5 mg / kg),布洛芬(4和15 mg / kg),双氯芬酸(2.5 mg / kg),氟比洛芬(2 mg / kg), celecoxib(7.5 mg / kg)和rofecoxib(1 mg / kg)单独或组合用于大鼠动脉血栓形成模型。每天口服药物治疗7天,然后插入动静脉分流血栓形成系统,放置15分钟。主要参数是血栓重量。每个实验使用5至12只大鼠,总共35只对照。阿司匹林以剂量依赖性方式抑制血栓形成。单独使用所有NSAIDS也会将血栓形成抑制到与阿司匹林1 mg / kg /天大致相同的水平。布洛芬,塞来昔布和罗非昔布抑制阿司匹林的作用,但不抑制双氯芬酸或氟比洛芬的作用。与阿司匹林的相互作用似乎并没有平等地影响所有的NSAID。需要在有足够动力的临床试验或药物流行病学研究中确认这种药物的临床影响。

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