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Perioperative plasma mitochondrial DNA dynamics and correlation with inflammation during infantile cardiopulmonary bypass

机译:婴儿体外循环期间血浆血浆线粒体DNA动力学及其与炎症的关系

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Objective Numerous studies in animals and humans have demonstrated that inflammatory mediators such as tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-8 play a role in cardiopulmonary bypass (CPB), which might affect surgical outcomes. Plasma mitochondrial DNA (mtDNA), a recently discovered pro-inflammatory agent, is released by cells upon insult. This study aimed to detect changes in plasma mtDNA levels at different time points after infantile CPB and explore its potential association with inflammatory mediators. Methods In the present study, we analyzed the perioperative plasma mtDNA and inflammatory cytokine levels of 48 infants undergoing ventricular septal defect closure. Blood samples were collected before aortic cross-clamping (T1), at the end of CPB (T2), and 6 h (T3), 12 h (T4), and 24 h (T5) post-CPB. Reverse transcription–polymerase chain reaction and specific enzyme-linked immunosorbent assay were used to quantify the plasma mtDNA and inflammatory cytokines, respectively. Bivariate correlation analysis was used to determine the correlations between plasma mtDNA and inflammatory cytokines. Results Plasma mtDNA levels increased at T2 and peaked at T3. Significant positive correlations were found between peak plasma mtDNA (at T3) and several inflammatory biomarkers, including IL-6 (at T3) (r = 0.62, P Conclusion Here we report that mtDNA may participate in a systemic inflammatory response to CPB.
机译:目的在动物和人类中进行的大量研究表明,炎症坏死因子(TNF)-α,白介素(IL)-6和IL-8等炎症介质在体外循环(CPB)中起作用,这可能会影响手术效果。血浆线粒体DNA(mtDNA)是一种最近发现的促炎剂,在受到侵害时会被细胞释放。这项研究旨在检测婴儿CPB后不同时间血浆mtDNA水平的变化,并探讨其与炎症介质的潜在关联。方法在本研究中,我们分析了48名接受室间隔缺损的婴儿的围手术期血浆mtDNA和炎性细胞因子水平。在CPB结束时(T2),CPB结束后6小时(T3),12小时(T4)和24小时(T5),在主动脉夹钳前(T1)采集血液样本。逆转录聚合酶链反应和特异性酶联免疫吸附试验分别用于定量血浆mtDNA和炎性细胞因子。使用双变量相关分析来确定血浆mtDNA与炎性细胞因子之间的相关性。结果血浆mtDNA水平在T2升高并在T3达到峰值。在血浆血浆mtDNA(在T3时)和几种炎症生物标记物之间存在显着的正相关性,包括IL-6(在T3时)(r = 0.62,P)结论在此我们报道mtDNA可能参与了对CPB的全身性炎症反应。

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