Thallinger Christiane, Rothenburger Markus, Marsik Claudia, Wuenscher Sonja, Popovic Martin, Endler Georg, Wagner Oswald, Joukhadar Christian
Division of Clinical Pharmacokinetics, Department of Clinical Pharmacology, University of Vienna, Vienna, Austria.
Pharmacology. 2008;81(1):57-62. doi: 10.1159/000108106. Epub 2007 Sep 11.
Recent studies have shown that distinct classes of antimicrobial agents might exert immunomodulatory effects in experimental settings. Daptomycin is the first member of the class of cyclic lipopeptide antibiotics, which exert their antimicrobial activity via a unique mode of action on the bacterial cytoplasmic membrane. Thus, we tested its ability to influence pro-inflammatory cytokines by use of an established experimental model of human endotoxemia.
A controlled experimental study design with 4 parallel groups was used. Whole blood from 10 healthy male volunteers was incubated either with saline (negative control), daptomycin (40 microg/ml, control), lipopolysaccharide (LPS; 50 pg/ml, positive control), or the combination of daptomycin plus LPS for 4 h. Real-time polymerase chain reaction was utilized for the measurement of selected pro-inflammatory cytokines, namely IL-1 beta, IL-6 (high sensitivity) and TNF-alpha on the mRNA level. Protein concentrations of these respective cytokines were measured in the supernatant using a commercially available ELISA.
Incubation of whole blood with LPS significantly increased protein and mRNA levels of cytokines compared to baseline (p < 0.05). However, the combination of daptomycin plus LPS did not exert any significant effect on mRNA and protein levels of IL-1 beta, IL-6 (high sensitivity) and TNF-alpha after 2 and 4 h of incubation compared to LPS incubation alone.
Daptomycin does not affect pro-inflammatory cytokines in the early phase of endotoxemia. This is most likely due to the unique mode of action of daptomycin, its low potential to penetrate into human cells and its high affinity to bacterial cytoplasmic membranes.
最近的研究表明,不同种类的抗菌剂在实验环境中可能发挥免疫调节作用。达托霉素是环脂肽类抗生素中的首个成员,它通过对细菌细胞质膜的独特作用方式发挥抗菌活性。因此,我们使用已建立的人类内毒素血症实验模型测试了其影响促炎细胞因子的能力。
采用具有4个平行组的对照实验研究设计。将来自10名健康男性志愿者的全血分别与生理盐水(阴性对照)、达托霉素(40微克/毫升,对照)、脂多糖(LPS;50皮克/毫升,阳性对照)或达托霉素加LPS的组合孵育4小时。利用实时聚合酶链反应在mRNA水平上测量选定的促炎细胞因子,即白细胞介素-1β、白细胞介素-6(高灵敏度)和肿瘤坏死因子-α。使用市售酶联免疫吸附测定法测量这些相应细胞因子在上清液中的蛋白质浓度。
与基线相比,全血与LPS孵育显著增加了细胞因子的蛋白质和mRNA水平(p<0.05)。然而,与单独LPS孵育相比,达托霉素加LPS的组合在孵育2小时和4小时后,对白细胞介素-1β、白细胞介素-6(高灵敏度)和肿瘤坏死因子-α的mRNA和蛋白质水平没有产生任何显著影响。
达托霉素在内毒素血症早期不影响促炎细胞因子。这很可能是由于达托霉素独特的作用方式、其穿透人类细胞的低潜力以及对细菌细胞质膜的高亲和力。