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先天性膈疝大鼠胸段静脉系统的显微磁共振成像

Microscopic magnetic resonance imaging of the thoracic venous system in rats with congenital diaphragmatic hernia.

作者信息

Luis A L, Bret M, Cuesta E, Aras R M, Xiaomei Liu, Encinas J L, Martinez L, Tovar J A

机构信息

Department of Pediatric Surgery, Hospital Universitario La Paz, Paseo de la Castellana, 261, 28046, Madrid, Spain.

出版信息

Pediatr Surg Int. 2011 Feb;27(2):175-80. doi: 10.1007/s00383-010-2789-9.

Abstract

BACKGROUND/AIM: Infants and rats with congenital diaphragmatic hernia (CDH) have malformations of the heart and the great arteries caused by neural crest (NC) dysregulation during embryogenesis. Abnormally narrow jugular veins have been found in babies during cannulation for ECMO. However, the venous system has not been examined in depth so far. We hypothesized that abnormal patterning and/or size of the thoracic veins could occur in rats with CDH. This hypothesis was tested by microscopic magnetic resonance imaging (MMRI), a high-resolution tool able to detect subtle changes of vessels in small animals.

MATERIAL/METHODS: Fetuses from pregnant rats fed either 100 mg i.g. nitrofen or vehicle on E9.5 were recovered near term. A 7 T MMRI system with a coronal multislice fast spin echo sequence allowed diagnosis of CDH (n = 19), and T2 SE high-resolution sequences made assessment of the pattern and width of cervico-thoracic veins possible. Values were corrected for body size by dividing them by the length of thoracic vertebrae T3-T5. The results in nitrofen and control (n = 11) groups were compared by non-parametric tests (*p < 0.05).

RESULTS

Congenital diaphragmatic hernia fetuses were smaller than controls (4.5 ± 0.26 vs. 5.3 ± 0.2 g*). The widths (corrected for body size) of left external, both innominate, right superior vena cava and azygos veins were significantly smaller in CDH rats than in controls.

CONCLUSIONS

The cervico-thoracic veins are normally patterned but abnormally narrow (except the internal jugulars) in rats with CDH. The same embryonic NC dysregulation that accounts for cardiovascular malformations could also explain these venous anomalies in CDH.

摘要

背景/目的:先天性膈疝(CDH)患儿及大鼠在胚胎发育过程中因神经嵴(NC)调节异常而出现心脏和大动脉畸形。在为接受体外膜肺氧合(ECMO)插管的婴儿中发现颈静脉异常狭窄。然而,迄今为止,静脉系统尚未得到深入研究。我们推测CDH大鼠可能出现胸段静脉的异常形态和/或大小改变。通过显微磁共振成像(MMRI)对这一推测进行了验证,MMRI是一种能够检测小动物血管细微变化的高分辨率工具。

材料/方法:在妊娠第9.5天给孕鼠经口灌胃100 mg硝基芬或赋形剂,接近足月时取出胎儿。使用配备冠状多层面快速自旋回波序列的7 T MMRI系统诊断CDH(n = 19),并通过T2 SE高分辨率序列评估颈胸段静脉的形态和宽度。将各项数值除以胸3至胸5椎体长度以校正体型。通过非参数检验比较硝基芬组和对照组(n = 11)的结果(*p < 0.05)。

结果

先天性膈疝胎儿比对照组小(4.5 ± 0.26 vs. 5.3 ± 0.2 g*)。CDH大鼠的左颈外静脉、双侧无名静脉、右头臂静脉和奇静脉的宽度(校正体型后)显著小于对照组。

结论

CDH大鼠的颈胸段静脉形态正常,但(除颈内静脉外)异常狭窄。导致心血管畸形的相同胚胎期NC调节异常也可能解释CDH中的这些静脉异常。

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