氨基视网膜神经元的电子显微镜。

Acta ophthalmologica. Supplementum Pub Date : 1982-01-01
I H Taylor
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引用次数: 0

摘要

电镜下观察了食蟹猴和家兔视网膜多巴胺能神经元的突触连接。在食蟹猴中,使用5,6-二羟色胺标记方法,而在兔子中使用单胺氧化酶抑制剂和(3H)-多巴胺放射自显影技术。5,6-二羟色胺标记法改变了多巴胺能神经元的正常超微结构,但其突触结构仍易于识别。放射自显影方法使标记神经元的超微结构保持不变,因此可以看到大而致密的囊泡与家兔的多巴胺能神经元有关。其他形态特征也可见。内核层核周多巴胺能分布和内丛状层多巴胺能过程与食蟹猴和家兔的无腺细胞一致。此外,多巴胺能过程具有无突细胞的常规特征的输出突触。在这两种动物中,多巴胺能过程都是突触前与无突细胞体相连,突触前和突触后与其他无突细胞相连。输出突触数大于输入突触数。序列和收敛的突触排列是常见的。用电镜观察了兔、猫、金鱼和鲤鱼视网膜中吲哚胺积聚神经元的突触组织。在干扰多巴胺能过程被破坏后,用5,6-二羟色胺标记神经元。三种动物的吲哚胺积累神经元均具有与无突细胞相似的核周和突起分布。它们也有传统的突触。在家兔和猫中,吲哚胺积累过程主要以内丛状层最内层的杆双极端互联突触为主。然而,它们也与其他无突细胞有突触前和突触后联系,在猫身上,它们与锥体双极细胞和神经节细胞的树突有突触接触。金鱼和鲤鱼的吲哚胺积累神经元主要是与其他无突细胞突触前和突触后,即使与双极终端也有接触。在金鱼和鲤鱼的视网膜内丛状层的中间部分发现了一个吲哚胺积累过程的子集,该过程具有一种以前未被识别的传统输出突触类型,具有两个突触后元件。这个突触被称为分支常规突触。在正常金鱼和鲤鱼的视网膜中发现并进行了研究。它的突触前结构被发现与某些具有突触前“球状星团”的传统突触相似,只有一个突触后元素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electron microscopy of aminergic retinal neurons.

The synaptic connections of the dopaminergic retinal neurons of Cynomolgus monkeys and rabbits were studied in the electron microscope. In the Cynomolgus monkeys, a labelling method with 5,6-dihydroxytryptamine was used, whereas an autoradiographic technique with a monoamine oxidase inhibitor and (3H)-dopamine was used in the rabbits. The labelling method with 5,6-dihydroxytryptamine altered the normal ultrastructure of the dopaminergic neurons, but their synaptic structures were still easily recognized. The autoradiographic method left the ultrastructure of the labelled neurons unchanged, and large dense-cored vesicles could therefore be seen to be associated with the dopaminergic neurons in the rabbits. Other morphological characteristics could also be seen. The distribution of dopaminergic perikarya in the inner nuclear layer and dopaminergic processes in the inner plexiform layer was consistent with that of amacrine cells in both Cynomolgus monkeys and rabbits. Furthermore, the dopaminergic processes had output synapses of the conventional kind characteristic of amacrine cells. In both animals, the dopaminergic processes were presynaptic to amacrine cell bodies and both pre- and postsynaptic to other amacrine cell processes. The number of output synapses was larger than the number of input synapses. Serial and convergent synaptic arrangements were common. The synaptic organization of the indoleamine-accumulating neurons in the retinae of rabbits, cats, goldfish and carp were also investigated in the electron microscope. The neurons were labelled with 5,6-dihydroxytryptamine after the otherwise interfering dopaminergic processes had been destroyed. The indoleamine-accumulating neurons of the three species had a distribution of perikarya and processes like that of amacrine cells. They also had synapses of the conventional kind. In the rabbit and the cat, the indoleamine-accumulating processes had mainly reciprocal synapses with rod bipolar terminals in the innermost part of the inner plexiform layer. They were, however, also also pre- and postsynaptic to other amacrine cells, and in the cat, they had synaptic contacts with cone bipolar cells and the dendrites of ganglion cells. The indoleamine-accumulating neurons of the goldfish and carp were mainly pre- and postsynaptic to other amacrine cells, even if contacts with bipolar terminals were also seen. In the retinae of goldfish and carp, a subset of indoleamine-accumulating processes were discovered in the middle part of the inner plexiform layer that had a previously not recognized type of conventional output synapse with two postsynaptic elements. This synapse was called a branched conventional synapse. It was found and investigated in the retinae of normal goldfish and carp. Its presynaptic structures were found to be similar to those seen in certain conventional synapses with presynaptic "globular clusters" and only one postsynaptic element.

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