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血管黏附蛋白-1 和 硫酸乙酰肝素蛋白聚糖-1 在感染性休克中的作用。

Vascular adhesion protein-1 and syndecan-1 in septic shock.

机构信息

Intensive Care Units, Division of Anaesthesia and Intensive Care Medicine, Helsinki University Hospital, Helsinki, Finland.

出版信息

Acta Anaesthesiol Scand. 2012 Mar;56(3):316-22. doi: 10.1111/j.1399-6576.2011.02578.x. Epub 2011 Dec 12.

DOI:10.1111/j.1399-6576.2011.02578.x
PMID:22150439
Abstract

BACKGROUND

Constituents of vascular endothelial surface layer (glycocalyx), e.g. an anchor protein syndecan-1 (SDC-1), can be detected in plasma in many inflammatory conditions. In inflammation, vascular adhesion protein-1 (VAP-1) is rapidly translocated to the apical side of the endothelial cells and may be released to plasma in a soluble form. We hypothesized that glycocalyx injury coincides with VAP-1 activation on endothelial cells. To test the hypothesis, we measured SDC-1 and VAP-1 levels in 20 patients with septic shock.

METHODS

A prospective observational study was conducted in two multidisciplinary critical care units in two tertiary academic teaching hospitals with 20 mechanically ventilated adult patients with septic shock, on days 1 and 4 of treatment. Twenty healthy adults were enrolled as a control group. Plasma SDC-1 content, serum VAP-1 activity, platelets, and leukocyte count were measured in septic shock group at baseline and at 72 h and compared with those of healthy controls.

RESULTS

VAP-1 activity and SDC-1 content were significantly increased in septic patients' group (P < 0.01) in comparison with controls. VAP-1 activity and SDC-1 content correlated positively to each other, and negatively to platelet count. In the septic shock group SDC-1 correlated on day 1 to SOFA score.

CONCLUSIONS

We found increased VAP-1 activity and SDC-1 content in critically ill patients with septic shock. Based on our results, the role of VAP-1 in shock pathogenesis should be studied with semicarbazide-sensitive amine oxidase activity blocking agents and substrate affinity testing.

摘要

背景

血管内皮表面层(糖萼)的成分,例如锚定蛋白 syndecan-1(SDC-1),在许多炎症情况下都可以在血浆中检测到。在炎症中,血管黏附蛋白-1(VAP-1)迅速向内皮细胞的顶端侧移位,并可能以可溶性形式释放到血浆中。我们假设糖萼损伤与内皮细胞上的 VAP-1 激活同时发生。为了验证这一假设,我们测量了 20 例脓毒性休克患者的 SDC-1 和 VAP-1 水平。

方法

在两家三级学术教学医院的两个多学科重症监护病房进行了一项前瞻性观察性研究,纳入了 20 例机械通气的成年脓毒性休克患者,在治疗的第 1 天和第 4 天进行测量。同时纳入 20 例健康成年人作为对照组。在基线和 72 小时时测量脓毒性休克组患者的血浆 SDC-1 含量、血清 VAP-1 活性、血小板和白细胞计数,并与健康对照组进行比较。

结果

与对照组相比,脓毒症患者组的 VAP-1 活性和 SDC-1 含量显著增加(P < 0.01)。VAP-1 活性和 SDC-1 含量相互之间呈正相关,与血小板计数呈负相关。在脓毒性休克组中,SDC-1 在第 1 天与 SOFA 评分相关。

结论

我们发现患有脓毒性休克的危重病患者的 VAP-1 活性和 SDC-1 含量增加。基于我们的结果,应该使用半卡巴嗪敏感胺氧化酶活性阻断剂和底物亲和力测试来研究 VAP-1 在休克发病机制中的作用。

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