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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effects of non-steroidal anti-inflammatory drugs on the luminol and lucigenin amplified chemiluminescence of human neutrophils.
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Effects of non-steroidal anti-inflammatory drugs on the luminol and lucigenin amplified chemiluminescence of human neutrophils.

机译:非甾体类抗炎药对人中性粒细胞的鲁米诺和发光素的化学发光作用。

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摘要

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.
机译:评估了一组通常用于治疗目的的非甾体类抗炎药对分离的人多形核中性粒细胞呼吸爆发的影响。用调理过的酵母刺激细胞,并通过放大的化​​学发光来检测活性氧物质的产生,所述化学发光是通过发光素和发光素进行的,发光素是测量不同细胞事件的两种发光剂。特别注意剂量效应曲线的建立和ED50的计算。测试的某些药物(醋乙胺,双氯芬酸,氟苯那酸和尼氟酸)能够以剂量依赖的方式降低鲁米诺和发光素的化学发光,反映出对呼吸爆发的抑制作用。最有效的衍生物是氟芬那酸(分别为ED50 8和78 microM,具有鲁米诺和光泽精),其次是双氯芬酸(21和98 microM),尼氟酸(97和227 microM)和醋乙胺(585和427 microM)。相比之下,其他几种药物(氟比洛芬,布洛芬,酮洛芬,吡罗昔康)刺激鲁米诺和发光素的化学发光,表明其具有促氧化剂活性。乙酰水杨酸(最高1250 microM)是适度的抑制剂(最大25%抑制),显示无剂量依赖性作用,托美汀(最高125 microM)在两个系统中均无明显作用。除消炎痛,萘普生和替诺昔康显示出不同的作用外,两种发光剂的结果均一致。使用的测量系统具有不确定性和复杂性,因此无法对结果进行完整的机械解释,但是与文献数据的比较为抗氧化剂和促氧化剂的作用提供了一些相关解释。

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