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Alterations in mitochondrial respiration and reactive oxygen species in patients poisoned with carbon monoxide treated with hyperbaric oxygen

机译:高压氧治疗一氧化碳中毒患者线粒体呼吸和活性氧的变化

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Abstract BackgroundCarbon monoxide (CO) poisoning is the leading cause of poisoning mortality and morbidity in the USA. Carboxyhemoglobin (COHb) levels are not predictive of severity or prognosis. At this time, the measurement of mitochondrial respiration may serve as a biomarker in CO poisoning. The primary objective of this study was to assess changes in mitochondrial function consisting of respiration and generation of reactive oxygen species (ROS) in peripheral blood mononuclear cells (PBMCs) obtained from patients with CO poisoning.MethodsPBMCs from patients having confirmed CO exposure treated with hyperbaric oxygen or HBO (CO group) and healthy controls (control group) were analyzed with high-resolution respirometry. PBMCs were placed in a 2-ml chamber at a final concentration of 3–4?×?106 cells/ml to simultaneously obtain both respiration and hydrogen peroxide (H2O2) production. In the CO group, we performed measurements before and after patients underwent their first HBO treatment.ResultsWe enrolled a total of 17 subjects, including 7 subjects with confirmed CO poisoning and 10 subjects in the control group. The CO group included five (71.4%) men and two (28.6%) women having a median COHb of 28%. There was a significant decrease in respiration as measured in pmol O2?×?s??1?×?10??6 PBMCs in the CO group (pre-HBO) when compared to the control group: maximal respiration (18.4?±?2.4 versus 35.4?±?2.8, P ?0.001); uncoupled Complex I respiration (19.8?±?1.8 versus 41.1?±?3.8, P? 0.001); uncoupled Complex I?+?II respiration (32.3?±?3.2 versus 58.3?±?3.1, P? 0.001); Complex IV respiration (43.5?±?2.9 versus 63.6?±?6.31, P ?0.05). There were also similar differences measured in the CO group before and after HBO treatment with an overall increase in respiration present after treatment. We also determined the rate of H2O2 production simultaneously with the measurement of respiration. There was an overall significant increase in the H2O2 production in the CO group after HBO treatment when compared to prior HBO treatment and the control group.ConclusionsIn this study, PBMCs obtained from subjects with CO poisoning have an overall decrease in respiration (similar H2O2 production) when compared to controls. The inhibition of Complex IV respiration is from CO binding leading to a downstream decrease in respiration at other complexes. PBMCs obtained from CO-poisoned individuals immediately following initial HBO therapy displayed an overall increase in both respiration and H2O2 production. The study findings demonstrate that treatment with HBO resulted in improved cellular respiration but a higher H2O2 production. It is unclear if the increased production of H2O2 in HBO treatment is detrimental.
机译:摘要背景一氧化碳(CO)中毒是美国中毒死亡率和发病率的主要原因。碳氧血红蛋白(COHb)水平不能预测严重程度或预后。此时,线粒体呼吸的测量可作为CO中毒的生物标志物。这项研究的主要目的是评估由CO中毒患者获得的外周血单核细胞(PBMC)的线粒体功能变化,包括呼吸作用和活性氧物种(ROS)的产生。氧或HBO(CO组)和健康对照组(对照组)均采用高分辨率呼​​吸测定法进行了分析。将PBMC放置在2 ml的小室中,最终浓度为3-4××106个细胞/ ml,以同时获得呼吸作用和过氧化氢(H2O2)的产生。在CO组中,我们在患者首次接受HBO治疗之前和之后进行了测量。结果我们共纳入了17名受试者,其中7名确诊为CO中毒的受试者和10名对照组的受试者。 CO组包括五名(71.4%)男性和两名(28.6%)女性,平均COHb为28%。与对照组相比,CO组(HBO之前)的pmol O2?×?s ?????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????????(88.4) 2.4对35.4±±2.8,P <0.001);非耦合的复杂I呼吸(19.8±±1.8与41.1±±3.8,P <0.001);无耦合的复合体I + + II呼吸(32.3±3.2相对58.3±3.1,P <0.001);复杂的IV呼吸(43.5±±2.9与63.6±±6.31,P <±0.05)。在HBO治疗之前和之后,CO组中也测出了相似的差异,治疗后呼吸的总体增加。我们还确定了H2O2产生的速率,同时测量了呼吸。与之前的HBO治疗和对照组相比,HBO治疗后CO组的H2O2排放量总体上显着增加。与控件相比。复合物IV呼吸的抑制来自CO结合,导致其他复合物呼吸的下游降低。最初进行HBO治疗后立即从CO中毒的个体获得的PBMC显示出呼吸和H2O2产生的总体增加。研究结果表明,HBO治疗可改善细胞呼吸作用,但可产生更高的H2O2。尚不清楚在HBO处理中H2O2产量的增加是否有害。

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