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非甾体抗炎药对人中性粒细胞鲁米诺和光泽精增强化学发光的影响。

Effects of non-steroidal anti-inflammatory drugs on the luminol and lucigenin amplified chemiluminescence of human neutrophils.

作者信息

Parij N, Nagy A M, Fondu P, Nève J

机构信息

Department of Organic Pharmaceutical Chemistry, Institute of Pharmacy, Free University of Brussels, Belgium.

出版信息

Eur J Pharmacol. 1998 Jul 10;352(2-3):299-305. doi: 10.1016/s0014-2999(98)00370-7.

Abstract

A panel of non-steroidal anti-inflammatory drugs commonly used for therapeutic purposes was assessed for their effects on the respiratory burst of isolated human polymorphonuclear neutrophils. Cells were stimulated with opsonised yeast and the production of reactive oxygen species was measured by amplified chemiluminescence with luminol and lucigenin which are two luminogenic agents measuring different cellular events. A special attention was devoted to the establishment of dose-effect curves and calculation of ED50. Some of the drugs tested (acemetacine, diclofenac, flufenamic acid and niflumic acid) were able to decrease both luminol and lucigenin chemiluminescence in a dose-dependent manner reflecting an inhibitory effect on the respiratory burst. The most potent derivative was flufenamic acid (ED50 8 and 78 microM, respectively, with luminol and lucigenin), followed by diclofenac (21 and 98 microM), niflumic acid (97 and 227 microM) and acemetacine (585 and 427 microM). In contrast, several other drugs (flurbiprofen, ibuprofen, ketoprofen, piroxicam) stimulated both luminol and lucigenin chemiluminescence, suggesting a pro-oxidant activity. Acetylsalicylic acid (up to 1250 microM) was a modest inhibitor (maximum 25% inhibition) showing no dose-dependent effect and tolmetin (up to 125 microM) had no significant effect in both systems. The results were in agreement using both luminogenic agents, except for indomethacin, naproxen and tenoxicam which showed different kinds of effects. The unspecific and complex nature of the measurement systems used did not allow to give a complete mechanistic interpretation of the results, but the comparison with literature data gave some pertinent explanations for both anti- and pro-oxidant effects.

摘要

对一组常用于治疗目的的非甾体抗炎药进行了评估,以研究它们对分离出的人多形核中性粒细胞呼吸爆发的影响。用调理酵母刺激细胞,通过使用鲁米诺和光泽精的增强化学发光法测量活性氧的产生,鲁米诺和光泽精是两种测量不同细胞事件的发光剂。特别关注剂量效应曲线的建立和半数有效剂量(ED50)的计算。所测试的一些药物(阿西美辛、双氯芬酸、氟芬那酸和尼氟酸)能够以剂量依赖的方式降低鲁米诺和光泽精化学发光,这反映了对呼吸爆发的抑制作用。最有效的衍生物是氟芬那酸(使用鲁米诺和光泽精时,ED50分别为8和78微摩尔),其次是双氯芬酸(21和98微摩尔)、尼氟酸(97和227微摩尔)和阿西美辛(585和427微摩尔)。相比之下,其他几种药物(氟比洛芬、布洛芬、酮洛芬、吡罗昔康)刺激了鲁米诺和光泽精化学发光,表明具有促氧化活性。乙酰水杨酸(高达1250微摩尔)是一种适度的抑制剂(最大抑制率为25%),未显示剂量依赖效应,托美丁(高达125微摩尔)在两个系统中均无显著作用。除吲哚美辛、萘普生和替诺昔康表现出不同类型的效应外,使用两种发光剂得到的结果一致。所使用的测量系统具有非特异性和复杂性,无法对结果进行完整的机理解释,但与文献数据的比较为抗氧化和促氧化作用提供了一些相关解释。

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