Ng Y K, Wong W C, Ling E A
Department of Anatomy, Faculty of Medicine, National University of Singapore.
J Hirnforsch. 1994;35(1):39-48.
The present study localised the superior salivatory nucleus (SSNc) in the reticular formation in rats using the retrograde axonal transport of fluorogold (FG). An ultrastructural study using the retrograde transport of horseradish peroxidase (HRP) was also carried out. After FG or cholera toxin conjugated-HRP (CT-HRP) injections into the lingual nerve, the labelling of SSNc in both the experiments was comparable. The retrogradely labelled cells were located in the ipsilateral parvocellular reticular formation (PCRt), dorsolateral to the facial nucleus and medial to the nucleus of the spinal tract of the trigeminal nerve. The rostrocaudal extent of the nucleus was about 0.9-1.05 mm, between the levels of the ascending facial nerve fibres caudally and the root of the facial nerve rostrally. The number of cells labelled was between 300-360, most of them being small to medium sized (14 x 22 mm) and appeared fusiform or polygonal. In rats receiving intraglandular injections of the tracers, the localisation and the rostrocaudal extent of the SSNc were similar, but the number of its containing labelled cells was only about 1/2 of the above. The SSNc cells that supplied the intra-glandular submandibular ganglion were not topographically arranged. On electron microscopy, the SSNc cells showed the typical features of preganglionic autonomic neurons. The cells contained a prominent round or oval nucleus. Their cytoplasm was rich in organelles especially conspicuous was the aggregations of the cisternae of rough endoplasmic reticulum in distinct clumps. In the neuropil between the SSNc cells were present numerous dendrites, axons, axon terminals and neuroglial cells. Most of the axon terminals contained predominantly round agranular vesicles with a few dense-cored or flattened agranular vesicles. The majority of the synapses associated with the HRP-labelled SSNc cells were on the dendrites with occasional axosomatic or axoaxonal synaptic contacts. A remarkable feature was the occurrence of synaptic contacts between HRP-labelled axons and some labelled soma.
本研究利用荧光金(FG)的逆行轴突运输对大鼠网状结构中的上泌涎核(SSNc)进行了定位。还进行了一项使用辣根过氧化物酶(HRP)逆行运输的超微结构研究。在将FG或霍乱毒素偶联的HRP(CT-HRP)注入舌神经后,两个实验中上泌涎核的标记情况相当。逆行标记的细胞位于同侧小细胞网状结构(PCRt)内,在面神经核的背外侧和三叉神经脊束核的内侧。该核的前后范围约为0.9 - 1.05毫米,在尾侧的面神经升支纤维水平与头侧的面神经根部水平之间。标记的细胞数量在300 - 360个之间,其中大多数为小到中等大小(14×22微米),呈梭形或多边形。在接受腺内注射示踪剂的大鼠中,上泌涎核的定位和前后范围相似,但其含标记细胞的数量仅约为上述数量的1/2。供应腺内下颌下神经节的上泌涎核细胞没有按拓扑结构排列。在电子显微镜下,上泌涎核细胞显示出节前自主神经元的典型特征。细胞含有一个突出的圆形或椭圆形细胞核。它们的细胞质富含细胞器,特别明显的是粗面内质网池在不同团块中的聚集。在上泌涎核细胞之间的神经毡中存在许多树突、轴突、轴突终末和神经胶质细胞。大多数轴突终末主要含有圆形无颗粒小泡,有一些致密核心或扁平无颗粒小泡。与HRP标记的上泌涎核细胞相关的大多数突触位于树突上,偶尔有轴-体或轴-轴突触联系。一个显著特征是HRP标记的轴突与一些标记的胞体之间存在突触联系。