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全层免疫组织化学揭示新生儿坏死性小肠结肠炎中肠神经系统的改变。

Alterations of the enteric nervous system in neonatal necrotizing enterocolitis revealed by whole-mount immunohistochemistry.

作者信息

Wedel T, Krammer H J, Kühnel W, Sigge W

机构信息

Department of Anatomy, Medical University of Lübeck, Germany.

出版信息

Pediatr Pathol Lab Med. 1998 Jan-Feb;18(1):57-70.

PMID:9566283
Abstract

Pathology reports on neonatal necrotizing enterocolitis (NNEC) rarely consider its effects on the enteric nervous system (ENS). Thus, the aim of this study has been to perform a two-dimensional assessment of neuropathologic lesions within the three ganglionated plexuses of the intestinal wall by means of whole-mount immunohistochemistry. Resected segments of ileum and colon affected by acute NNEC were submitted to immunohistochemical procedures using antibodies against neuronal (protein gene product 9.5) and glial (protein S-100, glial fibrillary acidic protein) proteins. Examination of the myenteric plexus and external submucosal plexus revealed a noticeable reduction in glial cells concomitant with the gradual deterioration of nerve cells, both findings predominating in the antimesenteric intestinal circumference, where ischemic lesions tend to appear first. The most severe damage of nervous tissue was observed in the plexus submucosus internus dependent on the depth of mucosal injury. The destroyed ganglia appeared like "empty baskets" (residual tangles) and housed deteriorated nerve and glial cells. Taking the anatomy of the intestinal vascular blood supply into consideration, the characteristic topography of neuropathologic lesions gives further support to an ischemic event within the cascade of different pathogenetic factors culminating in NNEC. Moreover, the demonstrated alterations of the ENS and their potential adverse effects on intestinal motility and neuroimmunologic interactions may contribute to the complex pathogenesis of NNEC, which remains a field of further investigation.

摘要

新生儿坏死性小肠结肠炎(NNEC)的病理报告很少考虑其对肠神经系统(ENS)的影响。因此,本研究的目的是通过整装免疫组织化学方法,对肠壁三个神经节丛内的神经病理损伤进行二维评估。将受急性NNEC影响的回肠和结肠切除段进行免疫组织化学处理,使用针对神经元(蛋白基因产物9.5)和神经胶质(蛋白S-100、胶质纤维酸性蛋白)蛋白的抗体。对肌间神经丛和外黏膜下神经丛的检查显示,神经胶质细胞明显减少,同时神经细胞逐渐退化,这两个发现主要出现在系膜对侧肠周径处,此处缺血性病变往往最先出现。根据黏膜损伤深度,在内侧黏膜下神经丛观察到最严重的神经组织损伤。被破坏的神经节看起来像“空篮子”(残留缠结),里面有退化的神经和神经胶质细胞。考虑到肠道血管血液供应的解剖结构,神经病理损伤的特征性地形分布进一步支持了在导致NNEC的不同致病因素级联反应中存在缺血事件。此外,所证明的ENS改变及其对肠道运动和神经免疫相互作用的潜在不利影响可能导致NNEC的复杂发病机制,这仍是一个有待进一步研究的领域。

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