Song Z M, Costa M, Brookes S J
Department of Human Physiology and Center for Neuroscience, The Flinders University of South Australia, Adelaide, Australia.
J Comp Neurol. 1998 Sep 21;399(2):255-68. doi: 10.1002/(sici)1096-9861(19980921)399:2<255::aid-cne8>3.0.co;2-#.
The distribution of submucous neurons that project to the myenteric plexus of the guinea pig small intestine was established by retrograde transport of the carbocyanine dye 1,1'-didodecyl-3,3,3',3'-tetramethyl indocarbocyanine perchlorate (DiI) from myenteric ganglia in organ culture in combination with immunohistochemistry. Following the application of DiI to the serosal surface of a single myenteric ganglion, from 2 to 15 DiI-labelled nerve cell bodies were labelled in the submucous plexus up to 7.9 mm circumferentially, 4.5 mm orally, and 3.4 mm aborally to the DiI application site. No cells were labelled in preparations in which connections between myenteric and submucous plexuses had been severed prior to DiI application. Cells that were immunoreactive for vasoactive intestinal polypeptide (VIP) or for substance P (SP) accounted for about 75% and 11% of DiI-labelled cells, respectively. Neither neuropeptide Y- nor calretinin-immunoreactive submucous neurons were labelled by DiI, indicating that these classes of neurons do not project to the myenteric plexus. Retrograde tracing from the myenteric plexus with Neurobiotin revealed that labelled VIP-immunoreactive neurons had several short, filamentous processes and a single long axon that could be followed through the circular muscle to myenteric ganglia without branches to the mucosa. The previously described projection of submucous, SP-immunoreactive putative sensory neurons to the myenteric plexus was confirmed. However, this study has identified a considerably larger population of presumed interneurons that are immunoreactive for VIP that likely transmit information from the submucous plexus to the myenteric plexus and presumably coordinate activity between the two ganglionated plexuses.
通过将花青染料1,1'-二癸基-3,3,3',3'-四甲基吲哚花青高氯酸盐(DiI)从器官培养的肌间神经节逆行运输,并结合免疫组织化学,确定了豚鼠小肠中投射到肌间神经丛的黏膜下神经元的分布。将DiI应用于单个肌间神经节的浆膜表面后,在黏膜下神经丛中标记到了2至15个DiI标记的神经细胞体,其周向距离DiI应用部位可达7.9毫米,口侧可达4.5毫米,肛侧可达3.4毫米。在DiI应用前已切断肌间和黏膜下神经丛之间连接的标本中未标记到细胞。对血管活性肠肽(VIP)或P物质(SP)免疫反应阳性的细胞分别占DiI标记细胞的约75%和11%。DiI未标记神经肽Y或钙视网膜蛋白免疫反应阳性的黏膜下神经元,表明这些类型的神经元不投射到肌间神经丛。用Neurobiotin从肌间神经丛进行逆行追踪显示,标记的VIP免疫反应阳性神经元有几个短的丝状突起和一条单一的长轴突,该轴突可穿过环形肌到达肌间神经节,且无分支至黏膜。先前描述的黏膜下SP免疫反应阳性的假定感觉神经元向肌间神经丛的投射得到了证实。然而,本研究发现了大量对VIP免疫反应阳性的假定中间神经元,它们可能将信息从黏膜下神经丛传递到肌间神经丛,并可能协调两个神经节神经丛之间的活动。