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喹诺酮类药物对人单核细胞产生肿瘤坏死因子的影响。

Effects of quinolones on tumor necrosis factor production by human monocytes.

作者信息

Bailly S, Fay M, Roche Y, Gougerot-Pocidalo M A

机构信息

INSERM U. 294, CHU Xavier Bichat, Paris, France.

出版信息

Int J Immunopharmacol. 1990;12(1):31-6. doi: 10.1016/0192-0561(90)90065-u.

Abstract

Previous studies have shown that in lipopolysaccharide (LPS)-stimulated human monocytes, interleukin 1 (IL-1) production is altered by quinoline derivative antibiotics (quinolones), in a way which depends both on the dose and on the agents used. Given that IL-1 and tumor necrosis factor alpha (TNF) are produced in response to LPS and have some overlapping and synergistic activities, we sought to determine if TNF production was altered under the above-mentioned conditions. We investigated the effects of three quinolones: ciprofloxacin (Cip), pefloxacin (Pef) and ofloxacin (Ofl). These quinolones were found to decrease extracellular TNF production in a dose-dependent manner at concentrations higher than 25 micrograms/ml as previously described by our laboratory with regard to IL-1 production. Moreover, the order of the extracellular decrease in TNF and IL-1 induced by each drug was similar. However, in contrast to IL-1 activity, the quinolones studied also reduced cell-associated TNF. The kinetics of TNF production suggested that the quinolones affected TNF production at a very early step, probably during TNF synthesis rather than during its secretion into the extracellular medium. Furthermore, the quinolone-induced accumulation of intracellular cAMP could explain the extracellular decrease in both IL-1 and TNF production.

摘要

先前的研究表明,在脂多糖(LPS)刺激的人单核细胞中,喹啉衍生物抗生素(喹诺酮类)会改变白细胞介素1(IL-1)的产生,其方式取决于剂量和所用药物。鉴于IL-1和肿瘤坏死因子α(TNF)是响应LPS而产生的,并且具有一些重叠和协同活性,我们试图确定在上述条件下TNF的产生是否会改变。我们研究了三种喹诺酮类药物的作用:环丙沙星(Cip)、培氟沙星(Pef)和氧氟沙星(Ofl)。正如我们实验室先前关于IL-1产生的描述,发现这些喹诺酮类药物在浓度高于25微克/毫升时以剂量依赖性方式降低细胞外TNF的产生。此外,每种药物诱导的细胞外TNF和IL-1降低的顺序相似。然而,与IL-1活性相反,所研究的喹诺酮类药物也降低了细胞相关的TNF。TNF产生的动力学表明,喹诺酮类药物在非常早期的阶段影响TNF的产生,可能是在TNF合成过程中,而不是在其分泌到细胞外介质的过程中。此外,喹诺酮类药物诱导的细胞内cAMP积累可以解释IL-1和TNF产生的细胞外降低。

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