Wickström Karin, Stavréus-Evers Anneli, Vercauteren Olivier, Olovsson Matts, Edelstam Greta
1 Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
2 Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Reprod Sci. 2017 Mar;24(3):382-392. doi: 10.1177/1933719116657188. Epub 2016 Jul 28.
The objective was to evaluate the effect of lignocaine on cytokine expression and secretion in vitro in peritoneal fluid macrophages and endometriotic stromal cells.
Experimental in vitro study on human cells.
Peritoneal fluid (n = 10) and samples from endometriotic cysts (n = 7) were collected from 13 women (women with endometriosis n = 8, and healthy controls n = 5) during surgery for clinical reasons.
Macrophages from the peritoneal fluid and cells from the inside of the endometriotic cysts capsules were isolated and cultivated for 24 to 48 hours in medium with and without the supplement of lignocaine 0.1 or 1.0 mg/mL. Relative gene expression of monocyte chemotactic protein 1 (MCP-1), interleukin 6 (IL-6), and IL-8 was evaluated with quantitative polymerase chain reaction and compared between treated and untreated cells with Wilcoxon matched pairs. The concentrations of MCP-1, IL-6, and IL-8 were measured using enzyme-linked immunosorbent assay and were compared between treated and untreated cells with Wilcoxon matched pairs.
The gene expression and protein secretion of IL-8 in endometriotic stromal cells after incubation with lignocaine 0.1 mg/mL were significantly decreased after 24 hours compared to the controls ( P = .028 and P = .018). Macrophages from healthy controls had a significant lower gene expression of all tested cytokines ( P = .043) after treatment with lignocaine, but there were no significant differences in protein level. Macrophages from women with endometriosis showed diverging results since 3 of 5 samples showed increased gene expression of 1 (n = 2) or 2 cytokines (n = 1) after lignocaine treatment.
Lignocaine can affect the gene expression and secretion of some proinflammatory cytokines in vitro.
评估利多卡因对体外培养的腹膜液巨噬细胞和子宫内膜异位症基质细胞中细胞因子表达和分泌的影响。
对人体细胞进行的体外实验研究。
因临床原因,在手术过程中从13名女性(8例子宫内膜异位症患者和5例健康对照)中收集了腹膜液(n = 10)和子宫内膜异位囊肿样本(n = 7)。
分离腹膜液中的巨噬细胞和子宫内膜异位囊肿囊壁内的细胞,在添加和不添加0.1或1.0 mg/mL利多卡因的培养基中培养24至48小时。采用定量聚合酶链反应评估单核细胞趋化蛋白1(MCP-1)、白细胞介素6(IL-6)和IL-8的相对基因表达,并使用Wilcoxon配对检验比较处理组和未处理组细胞。采用酶联免疫吸附测定法测量MCP-1、IL-6和IL-8的浓度,并使用Wilcoxon配对检验比较处理组和未处理组细胞。
与对照组相比,0.1 mg/mL利多卡因孵育24小时后,子宫内膜异位症基质细胞中IL-8的基因表达和蛋白分泌显著降低(P = .028和P = .018)。利多卡因处理后,健康对照的巨噬细胞中所有检测细胞因子的基因表达显著降低(P = .043),但蛋白水平无显著差异。子宫内膜异位症女性的巨噬细胞结果存在差异,因为5个样本中的3个在利多卡因处理后显示1种细胞因子(n = 2)或2种细胞因子(n = 1)的基因表达增加。
利多卡因在体外可影响某些促炎细胞因子的基因表达和分泌。