释放一氧化氮的非甾体抗炎药:一类新的gi保护抗炎药。

J L Wallace, Q J Pittman, G Cirino
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引用次数: 28

摘要

在一些常见的非甾体类抗炎药中加入一氧化氮释放片段可显著降低其在胃肠道中的毒性,而不会干扰其抑制前列腺素合成的能力。此外,一氧化氮释放的NSAID的抗炎和解热活性与母体化合物相当,而体内抗血栓活性明显增强。释放一氧化氮的非甾体抗炎药可能是现有的抗炎、退热和抗血栓药物的一种替代品,在胃肠道中的毒性大大降低。
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Nitric oxide-releasing NSAIDs: a novel class of GI-sparing anti-inflammatory drugs.

The addition of a nitric oxide-releasing moiety to a number of common nonsteroidal anti-inflammatory drugs markedly reduces their toxicity in the gastrointestinal tract without interfering with their ability to inhibit prostaglandin synthesis. Moreover, the anti-inflammatory and anti-pyretic activities of the nitric-oxide releasing NSAID were comparable to the parent compound, while the anti-thrombotic activity in vivo was significantly enhanced. Nitric oxide-releasing NSAIDs may represent an alternative to existing anti-inflammatory, anti-pyretic and anti-thrombotic agents with greatly reduced toxicity in the gastrointestinal tract.

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