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Systemic release of cytokines and heat shock proteins in porcine models of polytrauma and hemorrhage*

机译:猪多发伤和出血模型中细胞因子和热休克蛋白的系统释放*

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OBJECTIVE: To define systemic release kinetics of a panel of cytokines and heat shock proteins in porcine polytrauma/hemorrhage models and to evaluate whether they could be useful as early trauma biomarkers. DESIGN: Prospective observational study. SETTING: Research laboratory. SUBJECTS: Twenty-one Yorkshire pigs. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Pigs underwent polytrauma (femur fractures/lung contusion, P), hemorrhage (mean arterial pressure 25-30 mm Hg, H), polytrauma plus hemorrhage (P/H), or sham procedure (S). Plasma was obtained at baseline, in 5- to 15-min intervals during a 60-min shock period without intervention, and in 60- to 120-min intervals during fluid resuscitation for up to 300 min. Plasma was assayed for interleukin-1β, interleukin-4, interleukin-5, interleukin-6, interleukin-8, interleukin-10, interleukin-12/interleukin-23p40, interleukin-13, interleukin-17, interleukin-18, interferonγ, transforming growth factor-β, tumor necrosis factor-α, heat shock protein 40, heat shock protein 70, and heat shock protein 90 by enzyme-linked immunosorbent assay. All animals after S, P, and H survived (n = 5/group). Three of six animals after P/H died. Interleukin-10 increased during shock after P and this increase was attenuated after H. Tumor necrosis factor-α increased during the shock period after P, H, and also after S. P/H abolished the systemic interleukin-10 and tumor necrosis factor-α release and resulted in 20% to 30% increased levels of interleukin-6 during shock. As fluid resuscitation was initiated, tumor necrosis factor-α and interleukin-10 levels decreased after P, H, and P/H; heat shock protein 70 increased after P; and interleukin-6 levels remained elevated after P/H and also increased after P and S. CONCLUSIONS: Differential regulation of the systemic cytokine release after polytrauma and/or hemorrhage, in combination with the effects of resuscitation, can explain the variability and inconsistent association of systemic cytokine/heat shock protein levels with clinical variables in trauma patients. Insults of major severity (P/H) partially suppress the systemic inflammatory response. The plasma concentrations of the measured cytokines/heat shock proteins do not reflect injury severity or physiological changes in porcine trauma models and are unlikely to be able to serve as useful trauma biomarkers in patients.
机译:目的:确定猪多发性创伤/出血模型中一组细胞因子和热休克蛋白的系统释放动力学,并评估它们是否可用作早期创伤生物标志物。设计:前瞻性观察研究。地点:研究实验室。受试者:二十一头约克郡猪。干预措施:无。测量和主要结果:猪进行了多发伤(股骨骨折/肺挫伤,P),出血(平均动脉压25-30 mm Hg,H),多发伤加出血(P / H)或假手术(S)。在基线时,在无干预的60分钟休克期间以5至15分钟的间隔以及在进行液体复苏长达300分钟的过程中以60至120分钟的间隔获得血浆。测定血浆中的白介素-1β,白介素-4,白介素-5,白介素-6,白介素-8,白介素-10,白介素-12 /白介素-23p40,白介素-13,白介素-17,白介素18,干扰素γ,通过酶联免疫吸附法测定转化生长因子-β,肿瘤坏死因子-α,热休克蛋白40,热休克蛋白70和热休克蛋白90。 S,P和H之后的所有动物均存活(n = 5 /组)。 P / H死亡后六只动物中的三只。 P休克期间白细胞介素10升高,H减弱了这种增加。P,H和S休克后休克期肿瘤坏死因子-α增加。P/ H取消了全身白细胞介素10和肿瘤坏死因子- α释放并导致休克期间白介素6水平增加20%至30%。随着开始液体复苏,P,H和P / H后肿瘤坏死因子-α和白细胞介素10水平降低; P后热休克蛋白70增加;结论:多发伤和/或出血后全身细胞因子释放的差异调节,以及复苏的影响,可以解释变异性和不一致的关联,并且P / H后白细胞介素6水平仍然升高。患者的全身细胞因子/热休克蛋白水平与临床变量的关系严重程度(P / H)的损伤可部分抑制全身炎症反应。所测量的细胞因子/热休克蛋白的血浆浓度不能反映出猪创伤模型中的损伤严重程度或生理变化,因此不可能在患者中用作有用的创伤生物标志物。

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