Elekes K, Ravaille M, Bell C C, Libouban S, Szabo T
Neuroscience. 1985 Jun;15(2):417-29. doi: 10.1016/0306-4522(85)90223-4.
The medullary relay nucleus of the mormyrid weakly electric fish Gnathonemus petersii is a stage in the command pathway for the electric organ discharge. It receives input from the presumed command or pacemaker nucleus and projects to the electromotoneurons in the spinal cord. Its fine structure and synaptology were investigated by electron microscopy. The origin of the terminals contacting the cell membrane of the neurons of this nucleus was determined by horseradish peroxidase (HRP) injections into different brain structures, namely into the bulbar command- and mesencephalic command-associated nuclei. Twenty-five to thirty large cells of about 45 micron in diameter constitute the medullary electromotor relay. Each cell has a kidney-shaped, lobulated nucleus, a large myelinated axon with a short initial segment and several long, richly arborizing primary dendrites. Many, if not all, cells are interconnected with large somatosomatic or dendrosomatic, dendrodendritic and dendroaxonic gap junctions. These junctions often occur in serial or triadic arrangements. The relay cells receive large club endings as well as small boutons. The club endings are found mainly on the soma and primary dendrites and are morphologically mixed synapses. The boutons are characterized by synapses which are only chemical and are distributed all over the cell membrane, but with a definitely higher frequency on secondary dendrites and more distal parts of dendritic processes. Horseradish peroxidase injections into the mesencephalic command-associated nucleus reveal a large number of labelled boutons on the secondary dendrites of the relay cells. Injections into the bulbar command-associated nucleus label the same type of boutons as mesencephalic injections, but also label club endings on relay cell soma and primary dendrites. The results support the conclusion made on the basis of previous light microscopical observations that boutons originate from the bulbar command-associated nucleus, whereas the club endings issue from the presumed pacemaker nucleus (nucleus c). The club endings of the bifurcating axons of this nucleus are labelled by retro- and anterograde transport of horseradish peroxidase; the bifurcating axons project simultaneously to the bulbar command-associated nucleus and the medullary relay nucleus.
彼得氏裸臀鱼这种长颌鱼目弱电鱼的延髓中继核是电器官放电指令通路中的一个阶段。它接收来自假定的指令或起搏核的输入,并投射到脊髓中的电运动神经元。通过电子显微镜研究了其精细结构和突触学。通过将辣根过氧化物酶(HRP)注射到不同的脑结构中,即延髓指令相关核和中脑指令相关核,确定了与该核神经元细胞膜接触的终末的起源。25到30个直径约45微米的大细胞构成了延髓电运动中继。每个细胞都有一个肾形、分叶的细胞核,一条粗大的有髓轴突,其起始段较短,还有几条长的、分支丰富的初级树突。许多(如果不是全部的话)细胞通过大的体细胞间、树突-体细胞间、树突-树突间和树突-轴突间缝隙连接相互连接。这些连接常常以串联或三联的形式出现。中继细胞接收大型棒状终末以及小型轴突终扣。棒状终末主要见于胞体和初级树突,是形态学上的混合突触。轴突终扣的特征是仅为化学性突触,分布于整个细胞膜,但在次级树突和树突分支的更远端部分频率明显更高。将辣根过氧化物酶注射到中脑指令相关核中,可在中继细胞的次级树突上发现大量标记的轴突终扣。注射到延髓指令相关核中,标记的轴突终扣类型与注射到中脑时相同,但也标记中继细胞胞体和初级树突上的棒状终末。这些结果支持了基于先前光学显微镜观察得出的结论,即轴突终扣起源于延髓指令相关核,而棒状终末来自假定的起搏核(c核)。该核分支轴突的棒状终末通过辣根过氧化物酶的逆行和顺行运输进行标记;分支轴突同时投射到延髓指令相关核和延髓中继核。