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Effect of Lignocaine on IL-6, IL-8, and MCP-1 in Peritoneal Macrophages and Endometriotic Stromal Cells

机译:Lignocaine对IL-6,IL-8和MCP-1在腹膜巨噬细胞和子宫内膜异构体基质细胞中的影响

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Objective: The objective was to evaluate the effect of lignocaine on cytokine expression and secretion in vitro in peritoneal fluid macrophages and endometriotic stromal cells. Design: Experimental in vitro study on human cells. Population and Sample: 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. Methods: 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. Results: 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. Conclusion: Lignocaine can affect the gene expression and secretion of some proinflammatory cytokines in vitro.
机译:目的:目的是评估Limbocaine对腹膜流体巨噬细胞和子宫内膜体间质细胞体外细胞因子表达和分泌的影响。设计:人体细胞的实验体外研究。人口和样品:在手术期间,从13名妇女(患有子宫内膜异位症N = 8和健康对照N = 5)的腹膜液(n = 10)和来自子宫内膜胞囊性囊肿(n = 7)的样品进行临床原因。方法:从内膜静脉囊肿胶囊内部的腹膜液和细胞中的巨噬细胞分离,并在培养基中培养24至48小时,没有补充木质科因0.1或1.0mg / ml。用定量聚合酶链反应评价单核细胞趋化蛋白1(MCP-1),白细胞介素6(IL-6)和IL-8的相对基因表达,并在用紫烷氧基匹配对的处理和未处理的细胞之间进行比较。使用酶联免疫吸附试验测量MCP-1,IL-6和IL-8的浓度,并在用碘氧辛匹配对处理和未处理的细胞之间进行比较。结果:与对照相比,在24小时后,在与对照组24小时后,在Hignocaine 0.1mg / ml孵育后,IL-8中IL-8的基因表达和蛋白质分泌显着降低(P = .028和P = .018)。来自健康对照的巨噬细胞在用Lignocaine治疗后的所有测试细胞因子(P = 0.043)具有显着的较低基因表达,但蛋白质水平没有显着差异。具有子宫内膜异位症的女性的巨噬细胞显示出不同的结果,因为在木质科因治疗后,5个样品的3个样品增加了1(n = 2)或2个细胞因子(n = 1)的基因表达增加。结论:Lignocaine可以影响体外一些促炎细胞因子的基因表达和分泌。

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