精氨酸-抗利尿激素标志物copeptin是缺氧暴露的敏感血浆替代物

L. Ostergaard, A. Rudiger, S. Wellmann, Elena Gammella, B. Beck-Schimmer, J. Struck, M. Maggiorini, M. Gassmann
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引用次数: 14

摘要

研究背景供氧减少使患者面临组织缺氧、器官损伤甚至死亡的危险。作为回应,一些变化被激活,允许至少部分适应,从而增加生存的机会。我们的目的是研究精氨酸抗利尿激素标志物copeptin是否可以作为大鼠缺氧环境适应程度的标志。方法将Sprague-Dawley大鼠暴露于10%氧气环境48小时。测量动脉和右心室压力,并在设定的时间点进行血气分析。通过支气管肺泡灌洗、干湿体重测量和肺组织学检查肺部变化。采用新开发的特异性大鼠copeptin发光免疫分析法,研究了抗利尿素对缺氧反应的调节,并通过检测心房钠素(ANP)中部区域的proANP来研究心房钠素(ANP)。结果随着供氧量的减少,大鼠迅速变成紫绀型和失活型。尽管持续暴露在10%的氧气中,所有动物都在16小时内恢复并最终存活下来。他们的全身血压在急性(5分钟)缺氧时下降,但随着时间的推移部分恢复。相反,右心室压力在急性(5分钟)缺氧时升高,16小时后恢复正常。尽管长期缺氧,但未发现肺部炎症或水肿的迹象。急性缺氧(5分钟)后copeptin水平显著升高,16小时后恢复到接近基线水平,缺氧16小时后中部proANP水平进一步升高。结论血浆copeptin是急性(5分钟)严重缺氧暴露的敏感标志物,随后的调节可提示恢复。Copeptin水平因此可以反映临床和生理变化对缺氧的反应,并表明从持续的缺氧暴露恢复。
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Arginine-vasopressin marker copeptin is a sensitive plasma surrogate of hypoxic exposure
Background A reduced oxygen supply puts patients at risk of tissue hypoxia, organ damage, and even death. In response, several changes are activated that allow for at least partial adaptation, thereby increasing the chances of survival. We aimed to investigate whether the arginine vasopressin marker, copeptin, can be used as a marker of the degree of acclimatization/adaptation in rats exposed to hypoxia. Methods Sprague-Dawley rats were exposed to 10% oxygen for up to 48 hours. Arterial and right ventricular pressures were measured, and blood gas analysis was performed at set time points. Pulmonary changes were investigated by bronchoalveolar lavage, wet and dry weight measurements, and lung histology. Using a newly developed specific rat copeptin luminescence immunoassay, the regulation of vasopressin in response to hypoxia was studied, as was atrial natriuretic peptide (ANP) by detecting mid-regional proANP. Results With a decreasing oxygen supply, the rats rapidly became cyanotic and inactive. Despite continued exposure to 10% oxygen, all animals recuperated within 16 hours and ultimately survived. Their systemic blood pressure fell with acute (5 minutes) hypoxia but was partially recovered over time. In contrast, right ventricular pressures increased with acute (5 minutes) hypoxia and normalized after 16 hours. No signs of pulmonary inflammation or edema were found despite prolonged hypoxia. Whereas copeptin levels increased significantly after acute (5 minutes) hypoxia and then returned to near baseline after 16 hours, mid-regional proANP levels were even further increased after 16 hours of exposure to hypoxia. Conclusion Plasma copeptin is a sensitive marker of acute (5 minutes) exposure to severe hypoxia, and subsequent regulation can indicate recovery. Copeptin levels can therefore reflect clinical and physiological changes in response to hypoxia and indicate recovery from ongoing hypoxic exposure.
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