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尼美舒利对中性粒细胞衍生的次氯酸的灭活作用:炎症期间组织保护的潜在机制。

Inactivation of neutrophil-derived hypochlorous acid by nimesulide: a potential mechanism for the tissue protection during inflammation.

作者信息

Dallegri F, Patrone F, Ballestrero A, Ottonello L, Ferrando F, Sacchetti C

机构信息

First Medical Clinic, University of Genoa Medical School, Italy.

出版信息

Int J Tissue React. 1990;12(2):107-11.

PMID:2170285
Abstract

The anti-inflammatory drug nimesulide was found to effectively reduce the availability of hypochlorous acid, the most potent chlorinated oxidant generated by the myeloperoxidase system of activated neutrophils. Such an effect was observed at concentrations achievable in vivo after the oral administration of the drug. Higher concentrations of nimesulide were also found to limit both the oxygen consumption and the superoxide anion/hydrogen peroxide production by neutrophils. Taken together, the results suggest that nimesulide is endowed with a high potential to efficiently control the harmful effects of oxidants produced by neutrophils at inflammatory tissue sites.

摘要

抗炎药物尼美舒利被发现可有效降低次氯酸的生成量,次氯酸是活化中性粒细胞的髓过氧化物酶系统产生的最具活性的氯化氧化剂。口服该药物后,在体内可达到的浓度下观察到了这种效果。还发现较高浓度的尼美舒利可限制中性粒细胞的耗氧量以及超氧阴离子/过氧化氢的产生。综合来看,这些结果表明尼美舒利具有高效控制炎症组织部位中性粒细胞产生的氧化剂有害作用的巨大潜力。

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