Sawchenko P E, Swanson L W
Brain Res. 1982 Nov;257(3):275-325. doi: 10.1016/0165-0173(82)90010-8.
Axonal transport and immunohistochemical methods have been used to clarify the organization of pathways from noradrenergic and adrenergic cell groups in the brainstem to the paraventricular (PVH) and supraoptic (SO) nuclei of the hypothalamus. First, the location of such cells was determined with a combined retrograde tracer-immunofluorescence method. The fluorescent tracer, True Blue, was injected into the PVH or the SO, and sections through the brainstem were stained with anti-(rat) DBH, a specific marker for noradrenergic and adrenergic neurons. It was found that, after injections in the PVH, doubly labeled neurons were confined almost exclusively to 3 cell groups, the A1 region of the ventral medulla, which contained a majority of such cells, the A2 region in the dorsal vagal complex, and the locus coeruleus (A6 region). After injections centered in the SO an even greater proportion of doubly labeled cells were found in the A1 region, although some were also found in the A2 and A6 regions. The topography of doubly labeled cells indicates that these projections arise primarily from noradrenergic neurons, although adrenergic cells in both the C1 and the C2 groups probably contribute as well. Because well over 80% of the retrogradely labeled cells in these three regions were also DBH-positive, we next placed injections of [3H]amino acids into each of them in different groups of animals, and traced the course and distribution of the ascending (presumably DBH-positive) projections to the PVH and SO in the resulting autoradiograms. Injections centered in the A1 region labeled a substantial projection to most parts of the parvocellular division of the PVH, and was most dense in the dorsal and medial parts. In addition, terminal fields were labeled on those parts of the magnocellular division of the PVH, and of the SO, in which vasopressinergic cell bodies are concentrated. Injections centered in the A2 region also labeled a projection to the parvocellular division of the PVH that was topographically similar, but less dense, than that from the A1 region. In contrast, [3H]amino acid injections centered in the locus coeruleus labeled a moderately dense projection to the PVH that was limited to the medialmost part of the parvocellular division. Neither the A2 nor the A6 cell groups project to the magnocellular parts of PVH, or to the SO. The autoradiographic material, and additional double-labeling experiments, were used to identify and to characterize projections that interconnect the A1, A2 and A6 regions, as well as possible projections from these cell groups to the spinal cord. These results may be summarized as follows: a substantial projection from the nucleus of the solitary tract to the A1 region was identified, but this pathway does not arise from catecholaminergic neurons in the A2 cell group. DBH-stained cells in the A1 region project back to the dorsal vagal complex, as well as quite massively to the locus coeruleus (A6 region)...
轴突运输和免疫组织化学方法已被用于阐明从脑干中去甲肾上腺素能和肾上腺素能细胞群到下丘脑室旁核(PVH)和视上核(SO)的通路组织。首先,用逆行示踪剂 - 免疫荧光联合方法确定此类细胞的位置。将荧光示踪剂真蓝注入PVH或SO,然后用抗(大鼠)DBH对脑干切片进行染色,DBH是去甲肾上腺素能和肾上腺素能神经元的特异性标志物。结果发现,在PVH注射后,双重标记的神经元几乎仅局限于3个细胞群,即延髓腹侧的A1区,该区包含大多数此类细胞,迷走神经背侧复合体中的A2区,以及蓝斑(A6区)。以SO为中心注射后,在A1区发现的双重标记细胞比例更高,尽管在A2和A6区也发现了一些。双重标记细胞的拓扑结构表明,这些投射主要来自去甲肾上腺素能神经元,尽管C1和C2组中的肾上腺素能细胞可能也有贡献。由于这三个区域中超过80%的逆行标记细胞也是DBH阳性,接下来我们在不同组的动物中将[3H]氨基酸分别注入这三个区域,并在所得的放射自显影片中追踪向PVH和SO的上行(可能是DBH阳性)投射的行程和分布。以A1区为中心的注射标记了一条向PVH小细胞部大部分区域的大量投射,在背侧和内侧部分最为密集。此外,在PVH大细胞部以及SO中血管加压素能细胞体集中的部分也标记有终末场。以A2区为中心的注射也标记了一条向PVH小细胞部的投射,其拓扑结构与来自A1区的相似,但密度较小。相比之下,以蓝斑为中心的[3H]氨基酸注射标记了一条向PVH的中等密度投射,该投射仅限于小细胞部最内侧部分。A2和A6细胞群均不投射到PVH的大细胞部或SO。利用放射自显影材料以及额外的双重标记实验来识别和表征连接A1、A2和A6区域的投射,以及这些细胞群到脊髓的可能投射。这些结果可总结如下:确定了从孤束核到A1区的大量投射,但该通路并非来自A2细胞群中的儿茶酚胺能神经元。A1区中DBH染色的细胞投射回迷走神经背侧复合体,以及大量投射到蓝斑(A6区)……