McKellar S, Loewy A D
Brain Res. 1982 Jun 3;241(1):11-29. doi: 10.1016/0006-8993(82)91224-0.
Efferent connections of the region of the A1 catecholamine cell group were investigated by the anterograde autoradiographic method in rats, some of which had been pretreated with intraventricular injections of 6-hydroxydopamine (6-OHDA). Spinal projections were further studied by combining histofluorescence and horseradish peroxidase staining in the same sections. Projections from the A1 region ascend through the lateral hypothalamus to the bed nucleus of the stria terminalis, the medial preoptic area, and several hypothalamic nuclei: the dorsomedial nucleus, the dorsal hypothalamic area, the paraventricular and supraoptic nuclei, and the median eminence. These projections are predominantly ipsilateral. Since they are sensitive to 6-OHDA, they presumably arise from catecholamine cells of the A1 group. Other pathways are not noticeably affected by 6-OHDA. These include projections through the reticular formation to the contralateral nucleus ambiguus, the ipsilateral facial nucleus, and the Kölliker-Fuse nuclei, the parabrachial nuclei and the periaqueductal gray on both sides, as well as the intralaminar nuclei of the thalamus. These pathways probably do not arise from the A1 group, although a minor noradrenergic component cannot be ruled out. Spinal projections extend to the intermediolateral cell column and the ventral horn, and especially to the phrenic motor nucleus. However, these projections arise almost exclusively from non-catecholamine cells. Only a small minority of the fluorescent A1 cells are retrogradely labeled after injections of HRP into the upper thoracic spinal cord. They lie at the level of the pyramidal decussation. Likewise only a few fluorescent cells of the A2 group are labeled. Although the A1 and A2 groups were long thought to be principal sources of spinal norepinephrine, a review of the literature shows that this belief was based on equivocal evidence.
采用顺行性放射自显影法,在大鼠中研究了A1儿茶酚胺细胞群区域的传出联系,其中一些大鼠已预先经脑室注射6-羟基多巴胺(6-OHDA)进行预处理。通过在同一切片中结合组织荧光和辣根过氧化物酶染色,进一步研究脊髓投射。来自A1区域的投射通过外侧下丘脑向上延伸至终纹床核、内侧视前区以及几个下丘脑核:背内侧核、下丘脑背侧区、室旁核和视上核,以及正中隆起。这些投射主要是同侧的。由于它们对6-OHDA敏感,推测它们起源于A1组的儿茶酚胺细胞。其他通路未受到6-OHDA的明显影响。这些通路包括通过网状结构投射到对侧疑核、同侧面神经核以及双侧的 Kölliker-Fuse核、臂旁核和导水管周围灰质,以及丘脑的板内核。这些通路可能并非起源于A1组,尽管不能排除少量去甲肾上腺素能成分。脊髓投射延伸至中间外侧细胞柱和腹角,尤其是膈运动核。然而,这些投射几乎完全来自非儿茶酚胺细胞。将HRP注入上胸段脊髓后,只有一小部分荧光A1细胞被逆行标记。它们位于锥体交叉水平。同样,只有少数A2组的荧光细胞被标记。尽管长期以来人们一直认为A1和A2组是脊髓去甲肾上腺素的主要来源,但对文献的回顾表明,这种观点是基于不明确的证据。