Milos Scott, Hiansen Joshua Qua, Banaschewski Brandon, Zuo Yi Y, Yao Li-Juan, McCaig Lynda A, Lewis James, Yamashita Cory M, Veldhuizen Ruud A W
Lawson Health Research Institute, Department of Physiology and Pharmacology, Western University, London, ON, Canada.
Department of Mechanical Engineering, University of Hawaii at Manoa, Honolulu, HI, USA.
Biochem Biophys Rep. 2016 Sep;7:180-187. doi: 10.1016/j.bbrep.2016.06.009. Epub 2016 Jun 8.
Acute respiratory distress syndrome (ARDS) is a pulmonary disorder associated with alterations to the pulmonary surfactant system. Recent studies showed that supra-physiological levels of cholesterol in surfactant contribute to impaired function. Since cholesterol is incorporated into surfactant within the alveolar type II cells which derives its cholesterol from serum, it was hypothesized that serum hypercholesterolemia would predispose the host to the development of lung injury due to alterations of cholesterol content in the surfactant system. Wistar rats were randomized to a standard lab diet or a high cholesterol diet for 17-20 days. Animals were then exposed to one of three models of lung injury: i) acid aspiration ii) ventilation induced lung injury, and iii) surfactant depletion. Following physiological monitoring, lungs were lavaged to obtain and analyze the surfactant system. The physiological results showed there was no effect of the high cholesterol diet on the severity of lung injury in any of the three models of injury. There was also no effect of the diet on surfactant cholesterol composition. Rats fed a high cholesterol diet had a significant impairment in surface tension reducing capabilities of isolated surfactant compared to those fed a standard diet exposed to the surfactant depletion injury. In addition, only rats that were exposed to ventilation induced lung injury had elevated levels of surfactant associated cholesterol compared to non-injured rats. It is concluded that serum hypercholesterolemia does not predispose rats to altered surfactant cholesterol composition or to lung injury. Elevated cholesterol within surfactant may be a marker for ventilation induced lung damage.
急性呼吸窘迫综合征(ARDS)是一种与肺表面活性物质系统改变相关的肺部疾病。最近的研究表明,表面活性物质中胆固醇的超生理水平会导致功能受损。由于胆固醇在II型肺泡细胞内被整合到表面活性物质中,而II型肺泡细胞的胆固醇来源于血清,因此推测血清高胆固醇血症会因表面活性物质系统中胆固醇含量的改变,使宿主易发生肺损伤。将Wistar大鼠随机分为标准实验室饮食组或高胆固醇饮食组,持续17 - 20天。然后让动物暴露于三种肺损伤模型之一:i)酸吸入;ii)通气诱导性肺损伤;iii)表面活性物质耗竭。在进行生理监测后,对肺进行灌洗以获取并分析表面活性物质系统。生理结果显示,在三种损伤模型中的任何一种中,高胆固醇饮食对肺损伤的严重程度均无影响。饮食对表面活性物质的胆固醇组成也没有影响。与喂食标准饮食并暴露于表面活性物质耗竭损伤的大鼠相比,喂食高胆固醇饮食的大鼠分离出的表面活性物质降低表面张力的能力有显著损害。此外,与未受伤的大鼠相比,仅暴露于通气诱导性肺损伤的大鼠其表面活性物质相关胆固醇水平升高。得出的结论是,血清高胆固醇血症不会使大鼠易发生表面活性物质胆固醇组成改变或肺损伤。表面活性物质中胆固醇升高可能是通气诱导性肺损伤的一个标志物。