Descarries L, Bosler O, Berthelet F, Des Rosiers M H
J Physiol (Paris). 1981 Apr;77(1):53-61.
Precise knowledge of the ultrastructural features and interneuronal relationships of dopaminergic (DA) axon terminals or varicosities in neostriatum is still lacking. This ignorance is due to current limitations of the methods applicable to their specific visualization at electron microscopic level. High resolution radioautography, in particular, has not yet permitted a clearcut identification of the DA nerve endings which take up and store exogenous catecholamines in vivo, due to an apparent mobilization of tracer during standard histological preparative procedures for light and electron microscopy (Fig. 1 A). In this context, histological processing of the central nervous system by vascular perfusion, tested in adult rats subjected to prolonged lateroventricular instillation of [3H]DA, led to the following results and conclusions: 1 Axonal varicosities having accumulated [3H]DA in vivo may be detected in great number in the ipsilateral paraventricular neostriatum (Figs. 1 B and 1 C). 2 The specificity of this radioautographic labelling is evidenced by: (a) its disappearance or persistance, depending on the addition of a high concentration of non-radioactive noradrenaline or serotonin to the [3H]DA solution (Fig. 1 C); (b) the absence of labelled axonal varicosities in the supraependymal region (Figs. 2 E and 2 F) and suprachiasmatic nucleus (Fig. 1 E to be compared with 1 F) after administration of [3H]DA alone; (c) the absence of any localized accumulation of [3H]DA in neostriatum following prior destruction of the nigro-striatal DA system by 6-hydroxydopamine (Fig. 1 D). 3 It seems that carrying out the double fixation with glutaraldehyde and osmium by vascular perfusion is the prerequisite for retaining in situ the [3H]DA accumulated in vivo by neostriatal nerve endings. 4 Preliminary ultrastructural examination shows that the DA axonal varicosities of paraventricular neostriatum are of small caliber (mean diameter: 0.5 micron) and mostly contain clear synaptic vesicles, occasionally associated with a few larger dense-core vesicles (figs. 2 A-D). Several of these nerve endings establish axo-dendritic synaptic junctions (Fig. 2 C) and a few, perhaps, axo-somatic contacts (Fig. 2 D).
目前仍缺乏对新纹状体中多巴胺能(DA)轴突终末或膨体的超微结构特征及神经元间关系的确切认识。这种认知不足是由于目前适用于在电子显微镜水平对其进行特异性可视化的方法存在局限性。尤其是高分辨率放射自显影技术,由于在用于光镜和电镜检查的标准组织学制备过程中示踪剂明显移动,尚未能够清晰地识别在体内摄取和储存外源性儿茶酚胺的DA神经末梢(图1A)。在此背景下,通过血管灌注对成年大鼠进行中枢神经系统的组织学处理,在对其进行长时间侧脑室注入[3H]DA后,得出了以下结果和结论:1. 在同侧室旁新纹状体中可大量检测到在体内积累了[3H]DA的轴突膨体(图1B和1C)。2. 这种放射自显影标记的特异性体现在:(a)其消失或持续存在,这取决于在[3H]DA溶液中添加高浓度的非放射性去甲肾上腺素或血清素(图1C);(b)单独给予[3H]DA后,室管膜上区域(图2E和2F)和视交叉上核(图1E与1F对比)中无标记的轴突膨体;(c)在用6-羟基多巴胺预先破坏黑质-纹状体DA系统后,新纹状体中无[3H]DA的任何局部积累(图1D)。3. 似乎通过血管灌注用戊二醛和锇进行双重固定是原位保留新纹状体神经末梢在体内积累的[3H]DA的前提条件。4. 初步的超微结构检查表明,室旁新纹状体的DA轴突膨体口径较小(平均直径:0.5微米),且大多含有清亮突触小泡,偶尔伴有一些较大的致密核心小泡(图2A-D)。其中一些神经末梢形成轴-树突触连接(图2C),少数可能形成轴-体接触(图2D)。