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首页> 外文期刊>Intensive care medicine >Effect of L-NAME, an inhibitor of nitric oxide synthesis, on plasma levels of IL-6, IL-8, TNF alpha and nitriteitrate in human septic shock.
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Effect of L-NAME, an inhibitor of nitric oxide synthesis, on plasma levels of IL-6, IL-8, TNF alpha and nitriteitrate in human septic shock.

机译:一氧化氮合成抑制剂L-NAME对人败血症性休克中血浆IL-6,IL-8,TNFα和亚硝酸盐/硝酸盐的影响。

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OBJECTIVES: We tested the effects of NG-nitro-L-arginine methyl ester (L-NAME), an inhibitor of nitric oxide (NO) synthesis, on plasma levels of interleukin (IL) IL-6, IL-8, tumor necrosis factor-alpha (TNFalpha) and nitriteitrate (NO2-/ NO3-) in patients with severe septic shock. DESIGN: Prospective clinical study. SETTING: Surgical intensive care unit at a university hospital. PATIENTS: 11 consecutive patients with severe septic shock. INTERVENTIONS: Standard hemodynamic measurements were made and blood samples taken at intervals before, during, and after a 12-h infusion of L-NAME 1 mg x kg(-1) x h(-1) for determination of plasma IL-6, IL-8, TNFalpha and NO2-/NO3- concentration. MEASUREMENTS AND RESULTS: Patients with sepsis had increased plasma levels of IL-6, IL-8, TNFalpha and NO2-/NO3- (p < 0.05). Plasma levels of IL-6. IL-8, and NO2-/NO- were negatively correlated with systemic vascular resistance (r = -0.62, r = -0.65, and r = -0.78, respectively, all p < 0.05). Continuous infusion of L-NAME increased mean arterial pressure and systemic vascular resistance, with a concomitant reduction in cardiac output (all p < 0.01). No significant changes were seen in levels of plasma IL-6, IL-8, and NO-/NO3- during the 24-h observation period. Plasma levels of TNFalpha were significantly reduced during L-NAME infusion compared to baseline (p < 0.05). CONCLUSIONS: NO plays a role in the cardiovascular derangements of human septic shock. Inhibition of NO synthesis with L-NAME does not promote excessive cytokine release in patients with severe sepsis.
机译:目的:我们测试了一氧化氮(NO)合成抑制剂NG-硝基-L-精氨酸甲酯(L-NAME)对白细胞介素(IL)IL-6,IL-8和肿瘤坏死的血浆水平的影响严重败血症性休克患者中的α-因子(TNFalpha)和亚硝酸盐/硝酸盐(NO2- / NO3-)。设计:前瞻性临床研究。地点:大学医院的外科重症监护室。患者:连续11例严重败血症性休克患者。干预:进行标准的血流动力学测量,并在输注L-NAME 1 mg x kg(-1)xh(-1)12小时之前,之中和之后的时间间隔采集血样,以测定血浆IL-6,IL -8,TNFα和NO 2-/ NO 3-浓度。测量与结果:败血症患者血浆中IL-6,IL-8,TNFα和NO2- / NO3-的水平升高(p <0.05)。血浆IL-6水平。 IL-8和NO2- / NO-与全身血管阻力呈负相关(r分别为-0.62,r = -0.65和r = -0.78,所有p <0.05)。连续输注L-NAME会增加平均动脉压和全身血管阻力,并伴有心输出量下降(所有p <0.01)。在24小时观察期内,血浆IL-6,IL-8和NO- / NO3-的水平未见明显变化。与基线相比,L-NAME输注期间血浆TNFalpha的水平显着降低(p <0.05)。结论:NO在人类败血性休克的心血管紊乱中起作用。严重败血症患者用L-NAME抑制NO合成不会促进细胞因子的过度释放。

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