Zani Augusto, Cananzi Mara, Lauriti Giuseppe, Fascetti-Leon Francesco, Wells Jack, Siow Bernard, Lythgoe Mark F, Pierro Agostino, Eaton Simon, De Coppi Paolo
Department of Pediatric Surgery, University College London Institute of Child Health, London, United Kingdom.
Centre for Advanced Biomedical Imaging, University College London Institute of Child Health, London, United Kingdom.
Eur J Pediatr Surg. 2014 Feb;24(1):57-60. doi: 10.1055/s-0033-1350059. Epub 2013 Jul 12.
It has been demonstrated that in a neonatal rat model of necrotizing enterocolitis (NEC), amniotic fluid stem (AFS) cells decrease intestinal damage and improve survival via modulation of stromal cells expressing cyclooxygenase 2 in the lamina propria. Herein, we aimed to evaluate the effect of AFS cells on body weight and fluid retention in this NEC model. Methods AFS cells were obtained from green fluorescent protein (GFP) + pregnant rats at E16 and expanded in culture. A total of 185 neonatal rats had NEC induced by gavage feeding of hypertonic formula + hypoxia + oral lipopolysaccharide (4 mg/kg/d) and were randomized to intraperitoneal phosphate buffered saline (PBS, n = 93) or AFS cells (n = 92). A total of 36 breastfed (BF) rats were used as controls. All rats were being killed at 96 hours of life. Groups were compared for body weight and presence of free intraperitoneal fluid using nonparametric and contingency tests. Data are expressed as mean ± standard deviation.
There were no differences in birth weight among the groups (PBS = 5.6 ± 0. 3 g; AFS cells = 5.6 ± 0. 3 g; BF = 5.6 ± 0. 3 g; p = 1). The body weight at randomization was not different between PBS (5.61 ± 0. 5 g) and AFS cells (5.60 ± 0. 5; p = 1) rats. After the rats were killed, BF rats were significantly heavier (12.5 ± 0.1 g) than PBS (5.12 ± 0.4 g) and AFS cell rats (4.95 ± 0.3; p < 0.0001). From randomization to being killed, PBS rats had 9% of weight loss in comparison with 12% in AFS cell rats (p = 0.08). After the rats were killed, 42 (45%) PBS rats developed ascites with evident abdominal distension in comparison with 19 (21%) AFS cells (p = 0.0005). None of BF animals had ascites.
Gavage feeding and undernutrition severely affect growth in this model of NEC. Administration of AFS cells result in lower incidence of ascites than in PBS rats. This could explain the differences in body weight between the two groups of rats that were killed. Furthermore, studies on liver function and fluid composition are needed to investigate our speculation.
已证实,在坏死性小肠结肠炎(NEC)新生大鼠模型中,羊水干细胞(AFS)可通过调节固有层中表达环氧合酶2的基质细胞来减轻肠道损伤并提高存活率。在此,我们旨在评估AFS细胞对该NEC模型中体重和液体潴留的影响。方法:从妊娠16天的绿色荧光蛋白(GFP)+孕鼠获取AFS细胞,并在培养中进行扩增。总共185只新生大鼠通过灌胃高渗配方奶+低氧+口服脂多糖(4mg/kg/d)诱导发生NEC,并随机分为腹腔注射磷酸盐缓冲盐水(PBS,n = 93)组或AFS细胞(n = 92)组。总共36只母乳喂养(BF)大鼠用作对照。所有大鼠在出生96小时时处死。使用非参数检验和列联检验比较各组的体重和腹腔游离液体情况。数据以平均值±标准差表示。
各组间出生体重无差异(PBS = 5.6±0.3g;AFS细胞 = 5.6±0.3g;BF = 5.6±0.3g;p = 1)。随机分组时,PBS组(5.61±0.5g)和AFS细胞组(5.60±0.5g;p = 1)大鼠的体重无差异。大鼠处死时,BF大鼠(12.5±0.1g)明显重于PBS组(5.12±0.4g)和AFS细胞组大鼠(4.95±0.3g;p < 0.0001)。从随机分组到处死,PBS组大鼠体重减轻9%,而AFS细胞组大鼠体重减轻12%(p = 0.08)。大鼠处死时,42只(45%)PBS组大鼠出现腹水且腹部明显膨隆,相比之下,AFS细胞组有19只(21%)出现腹水(p = 0.0005)。BF组动物均未出现腹水。
在该NEC模型中,灌胃喂养和营养不良严重影响生长。给予AFS细胞导致腹水发生率低于PBS组大鼠。这可以解释两组处死大鼠之间体重的差异。此外,需要对肝功能和液体成分进行研究以探究我们的推测。