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释放一氧化氮的非甾体抗炎药:新型胃肠道保护药物。

Nitric oxide-releasing nonsteroidal anti-inflammatory drugs: novel gastrointestinal-sparing drugs.

作者信息

Bandarage U K, Janero D R

机构信息

NitroMed, Inc., Bedford, MA 01730, USA.

出版信息

Mini Rev Med Chem. 2001 May;1(1):57-70. doi: 10.2174/1389557013407160.

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) have unacceptable morbidity and mortality due to their gastrointestinal toxicity. Attempts so far to improve the safety profile of NSAIDs have met with limited clinical acceptance. Nitric oxide (NO) functions as an endogenous mediator of gastric mucosal health and defense. Recent medicinal chemistry approaches attempt to exploit the tissue-protective function of NO against NSAID-induced gastric injury. Both nitroxybutyl-ester and nitrosothiol NSAID derivatives have been synthesized. Profiling of these NO-donating NSAIDs in both the laboratory and the clinic suggests that they might offer a unique solution to the problem of NSAID-induced gastropathy without sacrificing the well-accepted pharmacological activity of these agents in the management of pain and inflammation.

摘要

非甾体抗炎药(NSAIDs)因其胃肠道毒性而具有不可接受的发病率和死亡率。迄今为止,改善NSAIDs安全性的尝试在临床上的接受程度有限。一氧化氮(NO)作为胃黏膜健康和防御的内源性介质发挥作用。最近的药物化学方法试图利用NO对NSAID诱导的胃损伤的组织保护功能。已合成了硝氧基丁酯和亚硝基硫醇NSAID衍生物。在实验室和临床中对这些释放NO的NSAIDs进行的分析表明,它们可能为NSAID诱导的胃病问题提供独特的解决方案,而不会牺牲这些药物在疼痛和炎症管理中广为人知的药理活性。

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