Church Joseph T, Perkins Elena M, Coughlin Megan A, McLeod Jennifer S, Boss Katherine, Bentley J Kelley, Hershenson Marc B, Rabah Raja, Bartlett Robert H, Mychaliska George B
Neonatology. 2018;113(4):313-321. doi: 10.1159/000486387. Epub 2018 Feb 23.
Extremely premature neonates suffer high morbidity and mortality. An artificial placenta (AP) using extracorporeal life support (ECLS) is a promising therapy.
We hypothesized that intratracheal perfluorocarbon (PFC) instillation during AP support would reduce lung injury and promote lung development relative to intratracheal amniotic fluid or crystalloid.
Lambs at an estimated gestational age (EGA) 116-121 days (term 145 days) were placed on venovenous ECLS with jugular drainage and umbilical vein reinfusion and intubated. Airways were managed by the instillation of amniotic fluid and tracheal occlusion (TO; n = 4), or lactated Ringer's (LR; n = 4) or perfluorodecalin (a PFC) without occlusion (n = 4). After 7 days, the animals were sacrificed. Early (EGA 116-121 days) and late (EGA 125-131 days) tissue control lambs were delivered and sacrificed. Lungs were formalin-inflated to 30 cm H2O and sectioned for histology. Injury was scored by an unbiased pathologist. Slides were immunostained for PDGFR-α and α-actin; development was quantified by the area fraction of double-positive tips. Surfactant protein-C (SP-C) concentration in bronchoalveolar lavage fluid was quantified using ELISA.
Total injury scores were lower in PFC lungs (1.8 ± 1.7) than in TO (6.5 ± 2.1; p = 0.01) and LR lungs (5.5 ± 2.4; p = 0.01). The area fraction of double-positive alveolar tips appeared higher in PFC lungs than in TO lungs (0.18 ± 0.007 vs. 0.008 ± 0.004; p = 0.07). SP-C concentration was higher in PFC lungs than in TO lungs (37.9 ± 7.6 vs. 20.0 ± 5.4 pg/mL; p = 0.005), and both early (12.4 ± 1.7 g/mL; p = 0.007) and late tissue control lungs (15.1 ± 5.0 pg/mL; p = 0.0008).
During AP support, intratracheal PFC prevents lung injury and promotes normal lung development better than crystalloid or amniotic fluid with TO.
极早产儿的发病率和死亡率很高。使用体外生命支持(ECLS)的人工胎盘(AP)是一种有前景的治疗方法。
我们假设在AP支持期间气管内滴注全氟碳化合物(PFC)相对于气管内滴注羊水或晶体液可减少肺损伤并促进肺发育。
估计胎龄(EGA)为116 - 121天(足月为145天)的羔羊接受颈静脉引流和脐静脉再灌注的静脉 - 静脉ECLS并插管。气道通过滴注羊水和气管闭塞(TO;n = 4),或乳酸林格氏液(LR;n = 4)或全氟萘烷(一种PFC)且不进行闭塞(n = 4)来处理。7天后,处死动物。分娩并处死早期(EGA 116 - 121天)和晚期(EGA 125 - 131天)的组织对照羔羊。将肺用福尔马林充气至30 cm H₂O并切片进行组织学检查。由一位公正的病理学家对损伤进行评分。玻片进行血小板衍生生长因子受体 - α(PDGFR - α)和α - 肌动蛋白免疫染色;通过双阳性尖端的面积分数对发育进行量化。使用酶联免疫吸附测定(ELISA)对支气管肺泡灌洗 fluid 中的表面活性蛋白 - C(SP - C)浓度进行量化。
PFC组肺的总损伤评分(1.8±1.7)低于TO组(6.5±2.1;p = 0.01)和LR组肺(5.5±2.4;p = 0.01)。PFC组肺中双阳性肺泡尖端的面积分数似乎高于TO组肺(0.18±0.007对0.008±0.004;p = 0.07)。PFC组肺中SP - C浓度高于TO组肺(37.9±7.6对20.0±5.4 pg/mL;p = 0.005),且高于早期(12.4±1.7 g/mL;p = 0.007)和晚期组织对照肺(15.1±5.0 pg/mL;p = 0.0008)。
在AP支持期间,气管内滴注PFC比使用TO的晶体液或羊水能更好地预防肺损伤并促进正常肺发育。