Hermel E E S, Faccioni-Heuser M C, Marcuzzo S, Rasia-Filho A A, Achaval M
Programa de Pós-Graduação em Neurociências, Universidade Federal do Rio Grande do Sul, Brazil.
J Anat. 2006 May;208(5):565-75. doi: 10.1111/j.1469-7580.2006.00559.x.
The aim of the present study was to describe the ultrastructure of neurons (from eight animals) and to analyse the synaptic terminal distribution (from two animals) in the posterodorsal subnucleus of the medial amygdala (MePD) of adult male rats. Using transmission electron microscopy, it was possible to identify many spiny and aspiny dendrites, unmyelinated axonal bundles, single axonal processes, a few myelinated axons, blood vessels and glial processes in the neuropil. Axodendritic synapses were the most frequently observed (67.5%), appearing to be of either the inhibitory or the excitatory types. The presynaptic region contained round or flattened vesicles that occurred either singly or with dense-cored vesicles (DCVs). The dendrites often received many synapses on a single shaft, and axon terminals displayed synaptic contacts with one or more postsynaptic structures. Dendritic spines showed different morphologies and the synapses on them (23.1%) formed a single and apparently excitatory synaptic contact with round, electron-lucid vesicles alone or, less frequently, with DCVs. Inhibitory and excitatory axosomatic synapses (8.2%) and excitatory axoaxonic synapses (1.2%) were also identified. The present report provides new findings relevant to the study of the MePD cellular organization and could be combined with other morphological data in order to reveal the functional activity of this area in male rats.
本研究的目的是描述成年雄性大鼠内侧杏仁核后背侧亚核(MePD)中神经元的超微结构(来自8只动物)并分析突触终末分布(来自2只动物)。使用透射电子显微镜,可以在神经毡中识别出许多有棘和无棘的树突、无髓轴突束、单个轴突、少数有髓轴突、血管和神经胶质突起。轴-树突触最为常见(67.5%),似乎是抑制性或兴奋性类型。突触前区域含有单个出现或与致密核心囊泡(DCV)一起出现的圆形或扁平囊泡。树突通常在单个轴干上接受许多突触,轴突终末与一个或多个突触后结构形成突触接触。树突棘呈现出不同的形态,其上的突触(23.1%)单独与圆形、电子透明囊泡或较少情况下与DCV形成单一且明显为兴奋性的突触接触。还识别出了抑制性和兴奋性轴-体突触(8.2%)以及兴奋性轴-轴突触(1.2%)。本报告提供了与MePD细胞组织研究相关的新发现,并且可以与其他形态学数据相结合,以揭示该区域在雄性大鼠中的功能活动。