Ito H, Sakamoto N, Takatsuji K
J Comp Neurol. 1982 Mar 1;205(3):299-311. doi: 10.1002/cne.902050310.
Cytoarchitecture and fiber connections of the nucleus isthmi in a teleost (Navodon modestus) were studied by means of Nissl, Bodian, toluidine blue, Golgi, and Fink-Heimer methods. Synaptic terminals were classified by the ultrastructural characteristics, and their origins were determined by electron microscopic degeneration experiments. The nucleus isthmi is composed of an outer cellular area or shell and an inner noncellular area or core. The shell covers anterior, dorsal, and ventral aspects of the core. The cell bodies in the shell are oval (15 x 20 micrometers) with an anteroposterior long axis, and have many somatic spines. Spines are also seen on the initial segment of the axon. Primary dendrites extend posteromedially and branch out in the core. The core contains thin and thick myelinated fibers, which originate in the optic tectum and in the nucleus pretectalis, respectively. At least two types of axon terminal were distinguished in the nucleus isthmi: S type, containing spherical vesicles, and F type, containing flattened vesicles. S terminals are derived from thin myelinated fibers and are only seen in the core where they form asymmetric synapses with dendrites. Frequently a portion of the S terminal membrane near the usual synaptic cleft is in close apposition with the membrane of an adjacent small dendrite or spine. F terminals, which derived from thick myelinated fibers, make symmetric synaptic contacts with both cell bodies in the shell and dendrites in the core. S terminals degenerate after ipsilateral ablation of the optic tectum, whereas F terminals degenerate after destruction of the nucleus pretectalis.
运用尼氏染色法、博迪安染色法、甲苯胺蓝染色法、高尔基染色法和芬克 - 海默染色法,对一种硬骨鱼(绿鳍马面鲀)峡核的细胞结构和纤维连接进行了研究。通过超微结构特征对突触终末进行分类,并通过电子显微镜下的变性实验确定其起源。峡核由一个外部细胞区域或壳层和一个内部无细胞区域或核心组成。壳层覆盖核心的前侧、背侧和腹侧。壳层中的细胞体呈椭圆形(15×20微米),长轴前后向,并有许多体细胞棘。在轴突的起始段也可见到棘。初级树突向后内侧延伸并在核心区域分支。核心区域包含细的和粗的有髓纤维,它们分别起源于视顶盖和顶盖前核。在峡核中至少区分出两种类型的轴突终末:S型,含有球形囊泡;F型,含有扁平囊泡。S终末来源于细的有髓纤维,仅见于核心区域,在那里它们与树突形成不对称突触。通常在常见突触间隙附近的S终末膜的一部分与相邻小树突或棘的膜紧密相邻。F终末来源于粗的有髓纤维,与壳层中的细胞体和核心区域中的树突都形成对称突触接触。同侧视顶盖切除后S终末变性,而顶盖前核破坏后F终末变性。