Munakata K, Tomita R, Kurosu Y
First Department of Surgery, Nihon University School of Medicine, Tokyo, Japan.
Eur J Pediatr Surg. 1997 Feb;7(1):21-9. doi: 10.1055/s-2008-1071043.
In order to investigate the causes of abnormal peristalsis of the colon in intestinal neuronal dysplasia (IND), we studied the structure of the myenteric plexus of IND colon using silver-impregnation (Suzuki's method) as well as the innervation of both IND colons and normal colons using immunofluorescence technique with monoclonal antibodies to synaptic vesicles, and antisera to vasoactive intestinal polypeptide (VIP), substance P (SP), methionine-enkephalin (Met-Enk), and gastrin-releasing peptide (GRP). The following results were obtained. 1) In the IND colon, the number of identifiable myenteric ganglia was decreased. In a few cases of IND, irreversible neuron degeneration can be involved in the pathogenesis of IND. 2) In the IND colon, the distribution and fluorescence intensity of synaptic vesicles coincided with those of peptidergic nerve fibers. In the normal colon, synaptic vesicles were much more numerous in the circular muscle layers than in the longitudinal muscle layers, and the fluorescence intensity of those in the circular muscle layers was stronger than that of those in the longitudinal muscle layers. On the other hand, in IND colon, there were fewer synaptic vesicles in the circular muscle layers, and their fluorescence intensity was weak, while there were many synaptic vesicles in the longitudinal muscle layers, and their fluorescence intensity was strong. 3) Morphological abnormalities may exist in synaptic vesicles in the circular muscle layers of the IND colon. 4) Regarding the peptidergic nerve fibers, in the IND colon, innervation of circular muscle layers by Met-Enk-, GRP- and SP-immunoreactive fibers was reduced, and longitudinal muscles were more strongly innervated by immunoreactive fibers than those in the normal colon. 5) Disturbed innervation of non-adrenergic non-cholinergic excitatory nerves may cause the disturbance of muscle contractions in the IND colon. In addition, an imbalance of peptidergic and synaptic vesicle's innervations in both muscle layers may be related to the abnormal peristalsis of IND colon. Also, morphological abnormalities of synaptic vesicles may be concerned with its abnormal peristalsis.
为了研究肠道神经元发育异常(IND)中结肠蠕动异常的原因,我们采用银浸染法(铃木法)研究了IND结肠肌间神经丛的结构,并使用针对突触小泡的单克隆抗体以及针对血管活性肠肽(VIP)、P物质(SP)、甲硫氨酸脑啡肽(Met-Enk)和胃泌素释放肽(GRP)的抗血清,通过免疫荧光技术研究了IND结肠和正常结肠的神经支配情况。获得了以下结果。1)在IND结肠中,可识别的肌间神经节数量减少。在少数IND病例中,不可逆的神经元变性可能参与了IND的发病机制。2)在IND结肠中,突触小泡的分布和荧光强度与肽能神经纤维的分布和荧光强度一致。在正常结肠中,环形肌层中的突触小泡比纵行肌层中的多,且环形肌层中突触小泡的荧光强度比纵行肌层中的强。另一方面,在IND结肠中,环形肌层中的突触小泡较少,其荧光强度较弱,而纵行肌层中有许多突触小泡,其荧光强度较强。3)IND结肠环形肌层中的突触小泡可能存在形态异常。4)关于肽能神经纤维,在IND结肠中,Met-Enk、GRP和SP免疫反应性纤维对环形肌层的神经支配减少,且纵行肌受免疫反应性纤维的神经支配比正常结肠中的更强。5)非肾上腺素能非胆碱能兴奋性神经的神经支配紊乱可能导致IND结肠中肌肉收缩的紊乱。此外,两层肌肉中肽能和突触小泡神经支配的失衡可能与IND结肠的异常蠕动有关。而且,突触小泡的形态异常可能与其异常蠕动有关。