纳布美酮是一种有效的抗炎剂,与硫丙酸和依托度酸相比,口服一个月对大鼠没有胃肠道刺激。

R Melarange, C Gentry, P R Blower, C D Toseland, R Spangler
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引用次数: 0

摘要

目的:比较纳布美酮在高抗炎剂量下口服1个月对大鼠的抗炎疗效和胃肠道刺激的影响,并与tiaprofenic acid和依托度酸进行比较。方法:以卡拉胶足跖水肿作为炎症模型。通过同时测量溃疡形成来评估胃肠道粘膜完整性。粘膜和组织前列腺素的产生和血浆触珠蛋白。盲肠内容物中的血红蛋白被用来衡量出血量。结果:纳布美酮、硫丙酸、依托多拉酸对炎症有抑制作用。依托度酸引起明显的胃肠损伤和失血,而硫丙酸仅引起胃损伤。纳布美酮不改变粘膜完整性。结论:那布美酮是一种无胃肠道刺激性的有效抗炎药。
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Nabumetone, an effective anti-inflammatory agent, lacks gastrointestinal irritancy in the rat when dosed orally for one month: comparison with tiaprofenic acid and etodolac.

Objective: To determine the effects of nabumetone, compared with tiaprofenic acid and etodolac, on anti-inflammatory efficacy and gastrointestinal irritancy in the rat when dosed orally for one month at a high anti-inflammatory dose.

Methods: Carrageenan paw edema was used as a model of inflammation. Gastrointestinal mucosal integrity was assessed by concurrently measuring ulcer formation. mucosal and tissue prostanoid production and plasma haptoglobin. Haemoglobin, present in the cecal contents, was used as a measure of blood loss.

Results: Nabumetone, tiaprofenic acid and etodolac inhibited inflammation. Etodolac induced marked gastrointestinal damage and blood loss whereas tiaprofenic acid caused only gastric damage. Nabumetone was found not to alter mucosal integrity.

Conclusion: Nabumetone proved to be an effective anti-inflammatory agent that was devoid of gastrointestinal irritancy.

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