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环丙沙星和吲哚美辛的联合应用抑制了巨噬细胞在体外分泌的炎症细胞因子的水平。

The combination of ciprofloxacin and indomethacin suppresses the level of inflammatory cytokines secreted by macrophages in vitro.

机构信息

School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, China; State Key Laboratory of Trauma, Burns and Combined Injury, Research Institute of Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.

State Key Laboratory of Trauma, Burns and Combined Injury, Research Institute of Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.

出版信息

Chin J Traumatol. 2022 Nov;25(6):379-388. doi: 10.1016/j.cjtee.2022.05.002. Epub 2022 May 16.

Abstract

PURPOSE

The combined use of antibiotics and anti-inflammatory medicine to manage bacterial endotoxin-induced inflammation following injuries or diseases is increasing. The cytokine level produced by macrophages plays an important role in this treatment course. Ciprofloxacin and indomethacin, two typical representatives of antibiotics and anti-inflammatory medicine, are cost-effective and has been reported to show satisfactory effect. The current study aims to investigate the effect of ciprofloxacin along with indomethacin on the secretion of inflammatory cytokines by macrophages in vitro.

METHODS

Primary murine peritoneal macrophages and RAW 264.7 cells were administrated with lipopolysaccharide (LPS) for 24 h. The related optimal dose and time point of ciprofloxacin or indomethacin in response to macrophage inflammatory response inflammation were determined via macrophage secretion induced by LPS. Then, the effects of ciprofloxacin and indomethacin on the secretory functions and viability of various macrophages were determined by enzyme-linked immunosorbent assay and flow cytometry analysis, especially for the levels of interleukin (IL)-1β, IL-6, IL-10, and tumor necrosis factor (TNF)-α. The optimal dose and time course of ciprofloxacin affecting macrophage inflammatory response were determined by testing the maximum inhibitory effect of the drugs on pro-inflammatory factors at each concentration or time point.

RESULTS

According to the levels of cytokines secreted by various macrophages (1.2 × 10 cells/well) after administration of 1 μg/mL LPS, the optimal dose and usage timing for ciprofloxacin alone were 80 μg/mL and 24 h, respectively, and the optimal dose for indomethacin alone was 10 μg/mL. Compared with the LPS-stimulated group, the combination of ciprofloxacin and indomethacin reduced the levels of IL-1β (p < 0.05), IL-6 (p < 0.05), IL-10 (p < 0.01)), and TNF-α (p < 0.01). Furthermore, there was greater stability in the reduction of inflammatory factor levels in the combination group compared with those in which only ciprofloxacin or indomethacin was used.

CONCLUSION

The combination of ciprofloxacin and indomethacin suppressed the levels of inflammatory cytokines secreted by macrophages in vitro. This study illustrates the regulatory mechanism of drug combinations on innate immune cells that cause inflammatory reactions. In addition, it provides a new potential antibacterial and anti-inflammatory treatment pattern to prevent and cure various complications in the future.

摘要

目的

抗生素和抗炎药物联合用于治疗损伤或疾病后细菌内毒素引起的炎症正在增加。巨噬细胞产生的细胞因子水平在这一治疗过程中起着重要作用。环丙沙星和吲哚美辛是抗生素和抗炎药物的两种典型代表,具有成本效益,并且已被报道具有令人满意的效果。本研究旨在探讨环丙沙星联合吲哚美辛对体外巨噬细胞炎症因子分泌的影响。

方法

用脂多糖(LPS)处理原代鼠腹腔巨噬细胞和 RAW 264.7 细胞 24 h。通过 LPS 诱导的巨噬细胞炎症反应,确定环丙沙星或吲哚美辛对巨噬细胞炎症反应的相关最佳剂量和时间点。然后,通过酶联免疫吸附试验和流式细胞术分析,特别是白细胞介素(IL)-1β、IL-6、IL-10 和肿瘤坏死因子(TNF)-α的水平,确定环丙沙星和吲哚美辛对各种巨噬细胞分泌功能和活力的影响。通过测试每种浓度或时间点药物对促炎因子的最大抑制作用,确定影响巨噬细胞炎症反应的环丙沙星最佳剂量和时间过程。

结果

根据 LPS 处理后(1.2×10 个细胞/孔)各种巨噬细胞分泌的细胞因子水平,环丙沙星单独使用的最佳剂量和使用时间分别为 80 μg/mL 和 24 h,而吲哚美辛单独使用的最佳剂量为 10 μg/mL。与 LPS 刺激组相比,环丙沙星和吲哚美辛联合使用降低了 IL-1β(p<0.05)、IL-6(p<0.05)、IL-10(p<0.01)和 TNF-α(p<0.01)的水平。此外,与单独使用环丙沙星或吲哚美辛相比,联合组炎症因子水平的降低更为稳定。

结论

环丙沙星和吲哚美辛联合抑制了体外巨噬细胞分泌的炎症细胞因子水平。本研究说明了药物组合对引起炎症反应的固有免疫细胞的调节机制。此外,它为未来预防和治疗各种并发症提供了一种新的潜在的抗菌和抗炎治疗模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcde/9751534/cd89332eed9e/gr1.jpg

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