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非甾体抗炎药不断变化的胃肠道副作用情况。预防新问题的新方法。

The changing gastrointestinal side effect profile of non-steroidal anti-inflammatory drugs. A new approach for the prevention of a new problem.

作者信息

Bjarnason I, Macpherson A

机构信息

Section of Gastroenterology, MRC Clinical Research Centre, Harrow, Middlesex, U.K.

出版信息

Scand J Gastroenterol Suppl. 1989;163:56-64. doi: 10.3109/00365528909091176.

Abstract

The most serious side effects of non-steroidal anti-inflammatory drugs (NSAIDs) involve gastroduodenal perforations and massive haemorrhage. It is becoming increasingly clear, however, that it is the small intestine that bears the main brunt of NSAID-related gastrointestinal toxicity. Hence 70% of patients receiving NSAIDs in the long term have evidence of small-intestinal inflammation, and the same patients lose blood and protein as a consequence. Many patients have asymptomatic ileal dysfunction and occasionally may develop unique small-intestinal strictures necesitating surgery. The pathogenesis of the intestinal inflammation is beginning to emerge. There are data to support that an imbalance between prostaglandins and leukotrienes is important in disrupting small-intestinal integrity during drug absorption. Furthermore, a simple mixture of glucose and citrate with indomethacin appears to minimize the damage. Whether this overcomes a metabolic block caused by NSAIDs and replenishes ATP levels or acts by scavenging oxygen free radicals is unknown, but our further understanding of the mechanism may revolutionize our approach to prevention of the gastrointestinal toxicity of NSAIDs.

摘要

非甾体抗炎药(NSAIDs)最严重的副作用包括胃十二指肠穿孔和大量出血。然而,越来越清楚的是,小肠首当其冲承受与NSAIDs相关的胃肠道毒性。因此,70%长期服用NSAIDs的患者有小肠炎症的证据,这些患者也因此失血和蛋白质流失。许多患者有无症状的回肠功能障碍,偶尔可能发展为需要手术治疗的独特小肠狭窄。肠道炎症的发病机制已开始显现。有数据支持,前列腺素和白三烯之间的失衡在药物吸收过程中破坏小肠完整性方面很重要。此外,葡萄糖、柠檬酸盐与消炎痛的简单混合物似乎能将损伤降至最低。这是克服了NSAIDs引起的代谢障碍并补充了ATP水平,还是通过清除氧自由基起作用尚不清楚,但我们对该机制的进一步了解可能会彻底改变我们预防NSAIDs胃肠道毒性的方法。

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