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ARDS 患儿肺泡 secretory phospholipase A2 活性的外植体效应研究。

Ex vivo effect of varespladib on secretory phospholipase A2 alveolar activity in infants with ARDS.

机构信息

Laboratory of Clinical Molecular Biology, Department of Biochemistry, University Hospital A. Gemelli, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

PLoS One. 2012;7(10):e47066. doi: 10.1371/journal.pone.0047066. Epub 2012 Oct 11.

Abstract

BACKGROUND

Secretory phospholipase A2 (sPLA2) plays a pivotal role in acute respiratory distress syndrome (ARDS). This enzyme seems an interesting target to reduce surfactant catabolism and lung tissue inflammation. Varespladib is a specifically designed indolic sPLA2 inhibitor, which has shown promising results in animals and adults. No specific data in pediatric ARDS patients are yet available.

METHODS

We studied varespladib in broncho-alveolar lavage (BAL) fluids obtained ex vivo from pediatric ARDS patients. Clinical data and worst gas exchange values during the ARDS course were recorded. Samples were treated with saline or 10-40-100 µM varespladib and incubated at 37°C. Total sPLA2 activity was measured by non-radioactive method. BAL samples were subjected to western blotting to identify the main sPLA isotypes with different sensitivity to varespladib. Results was corrected for lavage dilution using the serum-to-BAL urea ratio and for varespladib absorbance.

RESULTS

Varespladib reduces sPLA2 activity (p<0.0001) at 10,40 and 100 µM; both sPLA2 activity reduction and its ratio to total proteins significantly raise with increasing varespladib concentrations (p<0.001). IC(50) was 80 µM. Western blotting revealed the presence of sPLA2-IIA and -IB isotypes in BAL samples. Significant correlations exist between the sPLA2 activity reduction/proteins ratio and PaO(2) (rho = 0.63;p<0.001), PaO(2)/FiO(2) (rho = 0.7; p<0.001), oxygenation (rho = -0.6; p<0.001) and ventilation (rho = -0.4;p = 0.038) indexes.

CONCLUSIONS

Varespladib significantly inhibits sPLA2 in BAL of infants affected by post-neonatal ARDS. Inhibition seems to be inversely related to the severity of gas exchange impairment.

摘要

背景

分泌型磷脂酶 A2(sPLA2)在急性呼吸窘迫综合征(ARDS)中发挥着关键作用。这种酶似乎是减少表面活性剂分解和肺组织炎症的一个很有前途的靶点。Varespladib 是一种专门设计的吲哚 sPLA2 抑制剂,在动物和成人中已显示出良好的效果。但目前还没有儿科 ARDS 患者的具体数据。

方法

我们研究了 varespladib 在儿科 ARDS 患者体外支气管肺泡灌洗液(BAL)中的作用。记录了 ARDS 期间的临床数据和最差的气体交换值。用生理盐水或 10-40-100µM varespladib 处理样本,并在 37°C 下孵育。通过非放射性方法测量总 sPLA2 活性。用 Western blot 法鉴定对 varespladib 具有不同敏感性的主要 sPLA 同工型。结果用血清-支气管肺泡灌洗液尿素比和 varespladib 吸光度校正。

结果

在 10、40 和 100µM 时,varespladib 降低 sPLA2 活性(p<0.0001);随着 varespladib 浓度的增加,sPLA2 活性的降低及其与总蛋白的比值均显著升高(p<0.001)。IC50 为 80µM。Western blot 显示 BAL 样本中存在 sPLA2-IIA 和 -IB 同工型。sPLA2 活性降低/蛋白比与 PaO2(rho=0.63;p<0.001)、PaO2/FiO2(rho=0.7;p<0.001)、氧合(rho=-0.6;p<0.001)和通气(rho=-0.4;p=0.038)指数之间存在显著相关性。

结论

Varespladib 可显著抑制新生儿后 ARDS 患儿 BAL 中的 sPLA2。抑制作用似乎与气体交换损伤的严重程度呈负相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390d/3469496/287a9dc7c86a/pone.0047066.g001.jpg

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