De Luca Daniele, Vendittelli Francesca, Trias Joaquim, Fraser Heather, Minucci Angelo, Gentile Leonarda, Perez-Gil Jesus, Conti Giorgio, Antonelli Massimo, Capoluongo Ettore D
Lab di Biologia Molecolare Clinica - Serv. Analisi 1, Policlinico Universitario "A.Gemelli", Universita Cattolica del Sacro Cuore, L.go Agostino Gemelli 8, 00168 Roma.
Curr Pharm Biotechnol. 2013;14(4):445-8. doi: 10.2174/1389201011314040010.
Acute lung injury is a life-threatening condition characterized by surfactant dysfunction and raised secretory phospholipase A2 (sPLA2) activity. Varespladib is a sPLA2 inhibitor shown to be effective in animal models of acute lung injury. We aimed at investigating the effect of co-administration of surfactant and varespladib on sPLA2 activity. Alveolar macrophages were cultured and stimulated with lipopolysaccharide and then treated with either varespladib, surfactant, varespladib followed by surfactant or nothing. sPLA2 activity, free fatty acids, tumour necrosis factor-α (TNF-α) and protein concentrations were measured in culture supernatants. Treatment with varespladib (p=0.019) and varespladib + surfactant (p=0.013), reduced the enzyme activity by approximately 15% from the basal level measured in the untreated cultures. Surfactant, varespladib and varespladib + surfactant, respectively decreased free fatty acids by -45% (p=0.045), - 62% (p=0.009) and -48% (p=0.015), from the baseline concentration of the untreated cultures. Varespladib and poractant- α co-administration reduces sPLA2 activity and free fatty acids release in cultured rat alveolar macrophages, although a clear drug synergy was not evident. Since co-administration may be useful to reduce inflammation and surfactant inactivation in acute lung injury, further in vivo studies are warranted to verify its clinical usefulness.
急性肺损伤是一种危及生命的病症,其特征为表面活性剂功能障碍和分泌型磷脂酶A2(sPLA2)活性升高。伐瑞普拉迪布是一种sPLA2抑制剂,已证实在急性肺损伤动物模型中有效。我们旨在研究表面活性剂与伐瑞普拉迪布联合给药对sPLA2活性的影响。培养肺泡巨噬细胞,用脂多糖刺激,然后分别用伐瑞普拉迪布、表面活性剂、先给予伐瑞普拉迪布再给予表面活性剂或不进行处理。测量培养上清液中的sPLA2活性、游离脂肪酸、肿瘤坏死因子-α(TNF-α)和蛋白质浓度。用伐瑞普拉迪布(p=0.019)和伐瑞普拉迪布+表面活性剂(p=0.013)处理后,酶活性较未处理培养物中测得的基础水平降低了约15%。表面活性剂、伐瑞普拉迪布和伐瑞普拉迪布+表面活性剂分别使游离脂肪酸较未处理培养物的基线浓度降低了-45%(p=0.045)、-62%(p=0.009)和-48%(p=0.015)。联合给予伐瑞普拉迪布和猪肺磷脂可降低培养的大鼠肺泡巨噬细胞中的sPLA2活性和游离脂肪酸释放,尽管未观察到明显的药物协同作用。由于联合给药可能有助于减轻急性肺损伤中的炎症和表面活性剂失活,因此有必要进一步进行体内研究以验证其临床实用性。