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Prenatal intestinal obstruction affects the myenteric plexus and causes functional bowel impairment in fetal rat experimental model of intestinal atresia

机译:产前肠梗阻会影响肌间神经丛并导致胎鼠肠闭锁实验模型的功能性肠功能障碍

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摘要

Intestinal atresia is a rare congenital disorder with an incidence of 3/10 000 birth. About one-third of patients have severe intestinal dysfunction after surgical repair. We examined whether prenatal gastrointestinal obstruction might effect on the myenteric plexus and account for subsequent functional disorders. We studied a rat model of surgically induced antenatal atresia, comparing intestinal samples from both sides of the obstruction and with healthy rat pups controls. Whole-mount preparations of the myenteric plexus were stained for choline acetyltransferase (ChAT) and nitric oxide synthase (nNOS). Quantitative reverse transcription PCR was used to analyze mRNAs for inflammatory markers. Functional motility and permeability analyses were performed in vitro. Phenotypic studies were also performed in 8 newborns with intestinal atresia. In the experimental model, the proportion of nNOS-immunoreactive neurons was similar in proximal and distal segments (6.7 +/- 4.6% vs 5.6 +/- 4.2%, p = 0.25), but proximal segments contained a higher proportion of ChAT-immunoreactive neurons (13.2 +/- 6.2% vs 7.5 +/- 4.3%, p = 0.005). Phenotypic changes were associated with a 100-fold lower concentration-dependent contractile response to carbachol and a 1.6-fold higher EFS-induced contractile response in proximal compared to distal segments. Transcellular (p = 0.002) but not paracellular permeability was increased. Comparison with controls showed that modifications involved not only proximal but also distal segments. Phenotypic studies in human atresia confirmed the changes in ChAT expression. Experimental atresia in fetal rat induces differential myenteric plexus phenotypical as well as functional changes (motility and permeability) between the two sides of the obstruction. Delineating these changes might help to identify markers predictive of motility dysfunction and to define guidelines for post-surgical care.
机译:肠道闭锁是一种罕见的先天性疾病,出生率为3/10 000。约三分之一的患者在手术修复后出现严重的肠道功能障碍。我们检查了产前胃肠道阻塞是否可能对肌间神经丛产生影响,并解释了随后的功能障碍。我们研究了手术诱发的产前闭锁的大鼠模型,比较了梗阻两侧的肠样本和健康的幼崽对照。对整个肌腱神经丛制剂的胆碱乙酰基转移酶(ChAT)和一氧化氮合酶(nNOS)进行染色。定量逆转录PCR用于分析mRNAs中的炎症标志物。在体外进行功能运动性和通透性分析。还对8例肠道闭锁的新生儿进行了表型研究。在实验模型中,近端和远端段中nNOS免疫反应神经元的比例相似(6.7 +/- 4.6%与5.6 +/- 4.2%,p = 0.25),但近端段中ChAT免疫反应的比例更高神经元(13.2 +/- 6.2%vs 7.5 +/- 4.3%,p = 0.005)。表型变化与近段相比,对卡巴胆碱的浓度依赖性收缩反应降低100倍,而EFS诱导的收缩反应升高1.6倍。跨细胞(p = 0.002)但细胞旁通透性没有增加。与对照的比较表明,修饰不仅涉及近端片段,还涉及远端片段。人类闭锁的表型研究证实了ChAT表达的变化。胎儿大鼠的实验性闭锁会导致梗阻两侧之间的差异性肌间神经丛表型以及功能改变(运动性和通透性)。描绘这些变化可能有助于识别可预测运动功能障碍的标志物,并确定术后护理指南。

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