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Exogenous surfactant application in a rat lung ischemia reperfusion injury model: effects on edema formation and alveolar type II cells

机译:外源性表面活性剂在大鼠肺缺血再灌注损伤模型中的应用:对水肿形成和II型肺泡细胞的影响

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BackgroundProphylactic exogenous surfactant therapy is a promising way to attenuate the ischemia and reperfusion (I/R) injury associated with lung transplantation and thereby to decrease the clinical occurrence of acute lung injury and acute respiratory distress syndrome. However, there is little information on the mode by which exogenous surfactant attenuates I/R injury of the lung. We hypothesized that exogenous surfactant may act by limiting pulmonary edema formation and by enhancing alveolar type II cell and lamellar body preservation. Therefore, we investigated the effect of exogenous surfactant therapy on the formation of pulmonary edema in different lung compartments and on the ultrastructure of the surfactant producing alveolar epithelial type II cells.MethodsRats were randomly assigned to a control, Celsior (CE) or Celsior + surfactant (CE+S) group (n = 5 each). In both Celsior groups, the lungs were flush-perfused with Celsior and subsequently exposed to 4 h of extracorporeal ischemia at 4°C and 50 min of reperfusion at 37°C. The CE+S group received an intratracheal bolus of a modified natural bovine surfactant at a dosage of 50 mg/kg body weight before flush perfusion. After reperfusion (Celsior groups) or immediately after sacrifice (Control), the lungs were fixed by vascular perfusion and processed for light and electron microscopy. Stereology was used to quantify edematous changes as well as alterations of the alveolar epithelial type II cells.ResultsSurfactant treatment decreased the intraalveolar edema formation (mean (coefficient of variation): CE: 160 mm3 (0.61) vs. CE+S: 4 mm3 (0.75); p < 0.05) and the development of atelectases (CE: 342 mm3 (0.90) vs. CE+S: 0 mm3; p < 0.05) but led to a higher degree of peribronchovascular edema (CE: 89 mm3 (0.39) vs. CE+S: 268 mm3 (0.43); p < 0.05). Alveolar type II cells were similarly swollen in CE (423 μm3(0.10)) and CE+S (481 μm3(0.10)) compared with controls (323 μm3(0.07); p < 0.05 vs. CE and CE+S). The number of lamellar bodies was increased and the mean lamellar body volume was decreased in both CE groups compared with the control group (p < 0.05).ConclusionIntratracheal surfactant application before I/R significantly reduces the intraalveolar edema formation and development of atelectases but leads to an increased development of peribronchovascular edema. Morphological changes of alveolar type II cells due to I/R are not affected by surfactant treatment. The beneficial effects of exogenous surfactant therapy are related to the intraalveolar activity of the exogenous surfactant.
机译:背景预防性外源性表面活性剂治疗是减轻与肺移植相关的缺血和再灌注(I / R)损伤,从而减少急性肺损伤和急性呼吸窘迫综合征的临床发生的有希望的方法。但是,关于外源性表面活性剂减轻肺I / R损伤的方式的信息很少。我们假设外源性表面活性剂可能通过限制肺水肿的形成和增强肺泡II型细胞和片状体的保存而起作用。因此,我们研究了外源性表面活性剂治疗对不同肺区室中肺水肿形成以及对产生表面活性剂的肺泡上皮II型细胞超微结构的影响。方法将大鼠随机分配为对照,Celsior(CE)或Celsior +表面活性剂(CE + S)组(每组n = 5)。在两个Celsior组中,均用Celsior冲洗肺,然后在4°C下暴露于4小时的体外缺血,在37°C下暴露50分钟。 CE + S组在冲洗灌流前以50 mg / kg体重的剂量在气管内推注改性天然牛表面活性剂。再灌注后(Celsior组)或处死后(对照),通过血管灌注固定肺部,并进行光镜和电子显微镜检查。立体学用于量化水肿变化以及II型肺泡上皮细胞的变化。结果表面活性剂处理减少了肺泡内水肿的形成(平均值(变异系数):CE:160 mm3(0.61)vs.CE + S:4 mm3( 0.75); p <0.05)和不孕症的发展(CE:342 mm3(0.90)vs. CE + S:0 mm3; p <0.05),但导致较高的支气管周围血管水肿程度(CE:89 mm3(0.39))相对于CE + S:268 mm3(0.43); p <0.05)。与对照组(323μm3(0.07); p <0.05 vs. CE和CE + S)相比,CE(423μm3(0.10))和CE + S(481μm3(0.10))的肺泡II型细胞肿胀程度相似。与对照组相比,两个CE组的片状体数量均增加,平均片状体体积减少(p <0.05)。结论在I / R之前应用气管内表面活性剂可明显减少肺泡内水肿的形成和不饱和酶的产生,但导致支气管周围血管水肿的发展增加。 I / R引起的II型肺泡细胞的形态变化不受表面活性剂处理的影响。外源性表面活性剂治疗的有益作用与外源性表面活性剂的肺泡内活性有关。

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