首页> 外文期刊>The Lancet >Relation between muscle Na+K+ ATPase activity and raised lactate concentrations in septic shock: a prospective study.
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Relation between muscle Na+K+ ATPase activity and raised lactate concentrations in septic shock: a prospective study.

机译:败血性休克中肌肉Na + K + ATPase活性与乳酸浓度升高之间的关系:一项前瞻性研究。

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BACKGROUND: Hyperlactataemia during septic shock is often viewed as evidence of tissue hypoxia. However, this blood disorder is not usually correlated with indicators of perfusion or diminished with increased oxygen delivery. Muscles can generate lactate under aerobic conditions in a process linking glycolytic ATP supply to stimulation of Na+K+ ATPase. Using in-vivo microdialysis, we tested whether inhibition of Na+K+ ATPase can reduce muscle lactate. METHODS: In 14 patients with septic shock, two microdialysis probes were inserted into the quadriceps muscles and infused with lactate-free Ringer's solution in the absence or presence of 10(-7) mol/L ouabain, a specific inhibitor of Na+K+ ATPase. We measured lactate and pyruvate concentrations in both the dialysate fluid and arterial blood samples. FINDINGS: All patients had increased blood lactate concentrations (mean 4.0 mmol/L; SD 2.1). Lactate and pyruvate concentrations were consistently higher in muscle than in arteries during the study period, with a mean positive gradient of 1.98 mmol/L (SD 0.2; p=0.001) and 230 micromol/L (30; p=0.01), respectively. Ouabain infusion stopped over production of muscle lactate and pyruvate (p=0.0001). Muscle lactate to pyruvate ratios remained unchanged during ouabain infusion with no differences between blood and muscle. INTERPRETATION: Skeletal muscle could be a leading source of lactate formation as a result of exaggerated aerobic glycolysis through Na+K+ ATPase stimulation during septic shock. Lactate clearance as an end-point of resuscitation could therefore prove useful. RELEVANCE TO CLINICAL PRACTICE: In patients with septic shock, a high lactate concentration should be interpreted as a marker of disease, portending a bad outcome. The presence of hyperlactataemia in resuscitated septic patients should not be taken as proof of oxygen debt needing increases in systemic or regional oxygen transport to supranormal values. Lactate, instead of being regarded only as a marker of hypoxia, might be an important metabolic signal.
机译:背景:败血性休克期间的高乳酸血症常被视为组织缺氧的证据。但是,这种血液疾病通常与灌注指标无关,也不会随着氧气输送量的增加而减弱。在有氧条件下,肌肉可以在将糖酵解ATP供应与Na + K + ATPase刺激联系起来的过程中产生乳酸。使用体内微透析,我们测试了抑制Na + K + ATPase是否可以减少肌肉乳酸。方法:在14名败血性休克患者中,将两个微透析探针插入四头肌,并在不存在或存在10(-7)mol / L ouabain(一种Na + K + ATPase的特异性抑制剂)的情况下向其注入无乳酸林格氏液。 。我们测量了透析液和动脉血样品中乳酸和丙酮酸的浓度。结果:所有患者的血乳酸浓度均升高(平均4.0 mmol / L; SD 2.1)。在研究期间,肌肉中乳酸和丙酮酸的浓度始终高于动脉,平均正梯度分别为1.98 mmol / L(SD 0.2; p = 0.001)和230 micromol / L(30; p = 0.01)。哇巴因的输注因肌肉中乳酸和丙酮酸的产生而停止(p = 0.0001)。哇巴因输注过程中肌肉乳酸与丙酮酸的比率保持不变,血液和肌肉之间没有差异。解释:在败血性休克期间,由于Na + K + ATPase刺激而使有氧糖酵解过度,骨骼肌可能是乳酸形成的主要来源。乳酸清除作为复苏的终点因此可以证明是有用的。与临床实践的关系:在败血性休克患者中,高乳酸浓度应被解释为疾病的标志,预示不良结果。复苏的脓毒症患者中存在高乳酸血症,不能作为需要增加全身或局部氧气输送至超常值的氧气不足的证据。乳酸可能不是重要的代谢信号,而不是仅被视为缺氧的标志。

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