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首页> 外文期刊>Current pharmaceutical design >Animal models of gastric bleeding induced by dual antiplatelet therapy using aspirin and clopidogrel - Prophylactic effect of antiulcer drugs
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Animal models of gastric bleeding induced by dual antiplatelet therapy using aspirin and clopidogrel - Prophylactic effect of antiulcer drugs

机译:阿司匹林和氯吡格雷双重抗血小板疗法诱发的胃出血动物模型-抗溃疡药物的预防作用

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We set up two models of gastric bleeding in rats using low-dose aspirin (ASA) and the antiplatelet drug clopidogrel, a P2Y12 receptor antagonist, and examined the effect of antiulcer drugs on gastric bleeding and ulcerogenic responses under such conditions. Under urethane anesthesia, two catheters were inserted into the rat stomach, one from the esophagus and another through the pylorus via an incision in the duodenum. In the first model, the stomach was perfused with 25 mM ASA dissolved in 50 mM HCl using an infusion pump, and gastric bleeding was measured as the hemoglobin concentration in perfusate collected every 15 min. In the second model, the stomach was perfused with ASA under stimulation of acid secretion by a continuous i.v. infusion of histamine (8 mg/kg/hr). Clopidogrel (30 mg/kg) was given p.o. 24 h before the ASA perfusion, while antiulcer drugs were given i.d. or i.v. 30 min before. Perfusion of the stomach with acidified ASA or ASA under histamine-stimulated acid secretion caused minimal bleeding in the stomach with few lesions. The ulcerogenic and bleeding responses to ASA under these conditions were markedly aggravated by pretreatment with clopidogrel, which by itself provoked neither bleeding nor damage. Antiulcer drugs, such as prostaglandin E2, irsogladine, rebamipide and teprenone, reduced the severity of gastric bleeding and damage in response to ASA plus clopidogrel in the presence of both exogenous and endogenous acid. In contrast, antisecretory drugs such as a proton pump inhibitor and histamine H2 receptor antagonists markedly suppressed the gastric bleeding and lesion responses to ASA plus clopidogrel under histamine-stimulated acid secretion, but had no effect on the responses to acidified ASA plus clopidogrel. These results suggest that clopidogrel increases gastric bleeding induced by ASA and that antiulcer drugs are useful for preventing gastric bleeding caused by the dual antiplatelet therapy.
机译:我们使用低剂量阿司匹林(ASA)和抗血小板药物氯吡格雷(一种P2Y12受体拮抗剂)建立了大鼠胃出血的两种模型,并研究了抗溃疡药物在这种情况下对胃出血和溃疡发生反应的影响。在尿烷麻醉下,将两个导管插入大鼠的胃中,一个导管从食道插入,另一个导管通过幽门经十二指肠切口切入。在第一个模型中,使用输液泵向胃中灌注溶于50 mM HCl中的25 mM ASA,并以每15分钟收集的灌注液中的血红蛋白浓度来测量胃出血。在第二种模型中,在连续静脉输液刺激酸分泌的情况下,用ASA灌注胃。输注组胺(8 mg / kg / hr)。口服氯吡格雷(30 mg / kg)。在ASA灌注前24小时,同时内服抗溃疡药物。或i.v. 30分钟前在组胺刺激的酸分泌下用酸化ASA或ASA灌注胃,在胃中出血很少,几乎没有病变。在这种情况下,使用氯吡格雷预处理可明显加剧对ASA的致溃疡和出血反应,氯吡格雷本身不会引起出血或损害。在存在外源性和内源性酸的情况下,抗溃疡药(例如前列腺素E2,伊索拉定,瑞巴派特和替普瑞酮)可降低胃出血的严重程度和对ASA加氯吡格雷的反应引起的损害。相比之下,在组胺刺激的酸分泌下,质子泵抑制剂和组胺H2受体拮抗剂等抗分泌药物显着抑制了胃出血和对ASA加氯吡格雷的损伤反应,但对酸化ASA加氯吡格雷的反应没有影响。这些结果表明氯吡格雷增加了由ASA引起的胃出血,并且抗溃疡药物可用于预防由双重抗血小板疗法引起的胃出血。

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