Lipsett J, Cool J C, Runciman S I, Ford W D, Kennedy J D, Martin A J, Parsons D W
Department of Histopathology, Women's and Children's Hospital, North Adelaide, South Australia 5006, Australia.
Pediatr Dev Pathol. 2000 Jan-Feb;3(1):17-28. doi: 10.1007/s100240050002.
Congenital diaphragmatic hernia (CDH) in humans carries high mortality/morbidity attributed to associated pulmonary hypoplasia. An understanding of the effects of CDH on fetal lung growth is important for development of successful treatments. This study aimed to quantitate structural differences between normal and CDH-affected preterm lamb lungs. We hypothesized that (a) pulmonary hypoplasia is present in preterm CDH-affected lungs; (b) the relative degree of pulmonary hypoplasia increases with gestation; and (c) the left upper lobe (LUL) is affected most. Fetal lambs were allocated to two groups. One group underwent surgery (72-74 days gestation) inducing CDH. Both groups (n = 7, n = 7) were delivered by cesarean section at 129 days (term: 145-149). Lungs were obtained at autopsy, were inflation-fixed, processed for histology, and morphometry was performed. Preterm lungs of CDH-affected lambs in comparison to those of normal lambs demonstrated a reduction in the following: lung weight (37.7 g vs. 116.3 g); lung weight:body weight (0.012 vs. 0.040); fixed lung volume (33.6 ml vs. 96.9 ml); gas-exchange surface area (4.56 m(2) vs. 13.70 m(2)); parenchyma:nonparenchyma (59:41 vs. 72:28); and parenchymal airspace:tissue (16:84 vs. 35:65). Non-parenchyma connective tissue was increased (58%), airspaces were more numerous (1077/mm(2)) and smaller (perimeter 76.6 microm), gas-exchange surface density (2394 cm(-1)) was greater and capillary loading (0.04 ml/m(2)) was reduced compared to preterm normal lung (49%; 778/mm(2); 108.7 microm; 2003 cm(-1), 0.11 ml/m(2), respectively). The LUL was affected most. These data quantitate pulmonary hypoplasia in preterm CDH-affected lambs. Comparisons with published data indicate increasing relative hypoplasia as gestation proceeds. Fetal interventions will affect lung development, depending on timing, with intervention still likely to be worthwhile during late gestation.
人类先天性膈疝(CDH)由于伴有肺发育不全,死亡率/发病率很高。了解CDH对胎儿肺生长的影响对于成功治疗方法的开发很重要。本研究旨在量化正常早产羔羊肺与患CDH早产羔羊肺之间的结构差异。我们假设:(a)患CDH的早产羔羊肺存在肺发育不全;(b)肺发育不全的相对程度随孕周增加;(c)左上叶(LUL)受影响最大。将胎羊分为两组。一组在妊娠72 - 74天时接受手术诱导CDH。两组(每组n = 7)均在妊娠129天时剖宫产分娩(足月:145 - 149天)。在尸检时获取肺,进行充气固定,处理后用于组织学检查,并进行形态计量学分析。与正常早产羔羊肺相比,患CDH早产羔羊肺在以下方面有所减少:肺重量(37.7克对116.3克);肺重量与体重之比(0.012对0.040);固定肺体积(33.6毫升对96.9毫升);气体交换表面积(4.56平方米对13.70平方米);实质与非实质比例(59:41对72:28);实质气腔与组织比例(16:84对35:65)。非实质结缔组织增加(58%),气腔更多(1077个/平方毫米)且更小(周长76.6微米),气体交换表面密度(2394平方厘米⁻¹)更大,与正常早产肺相比,毛细血管负荷(0.04毫升/平方米)降低(分别为49%;778个/平方毫米;108.7微米;2003平方厘米⁻¹,0.11毫升/平方米)。左上叶受影响最大。这些数据量化了患CDH早产羔羊肺的肺发育不全情况。与已发表数据的比较表明,随着孕周增加,相对发育不全加剧。胎儿干预将影响肺发育,这取决于干预时机,在妊娠晚期进行干预仍可能是值得的。