Wiegand S J, Price J L
J Comp Neurol. 1980 Jul 1;192(1):1-19. doi: 10.1002/cne.901920102.
The cell bodies of origin of axons terminating in the median eminence have been identified by retrograde axonal transport of horseradish peroxidase (HRP) or 125I-wheat germ agglutinin (WGA). The tracers were injected into the median eminence by pressure and under direct visual control, using a ventral surgical approach. The retrogradely labeled cells are exclusively located within the hypothalamus. The most heavily labeled cells are parvocellular neurons in the arcuate nucleus, the periventricular area, the medial part of the paraventricular nucleus, and the rostral paraventricular nucleus; a few cells are also located in the rostral part of the preoptic area immediately lateral and dorsal to the organum vasculosum of the lamina terminalis (OVLT). Less heavily located cells are found in the magnocellular neurosecretory nuclei, including the lateral parts of the paraventricular and rostral paraventricular nuclei, the supraoptic nucleus, and the accessory magnocellular nuclei. Retrogradely labeled cells are not found in the ventromedial hypothalamic nucleus, except for a few lightly labeled cells in the posterior division of the nucleus. However, if the injected tracer spreads into the arcuate nucleus, labeled cells are present throughout the ventromedial nucleus. Labeled cells are not found in other parts of the hypothalamus, including lateral and posterior portions of the preoptic area, the anterior hypothalamic area, and the suprachiasmatic nucleus, or in catecholaminergic cell groups of the midbrain, pons, and medulla. Control injections of HRP into the posterior pituitary and the ventromedial nucleus produce patterns of cell labeling which are very distinct from that seen with injections into the median eminence. Following injections into the posterior pituitary, the cells of the magnocellular neurosecretory nuclei are all heavily labeled, but small cells in the parvocellular neuronal groups are not labeled. Direct injections into the ventromedial nucleus resulted in labeled cells in widespread parts of the hypothalamus, as well as in the bed nucleus of the stria terminalis and the lateral septum, in parts of the amygdaloid complex and the subiculum, and in several cell groups in the midbrain, pons, and medulla.
通过辣根过氧化物酶(HRP)或125I-小麦胚凝集素(WGA)的逆行轴突运输,已确定终止于正中隆起的轴突的起始细胞体。使用腹侧手术入路,在直接视觉控制下通过压力将示踪剂注入正中隆起。逆行标记的细胞仅位于下丘脑内。标记最密集的细胞是弓状核、室周区、室旁核内侧部分和室旁核嘴侧部分的小细胞神经元;少数细胞也位于终板血管器(OVLT)外侧和背侧紧挨着的视前区嘴侧部分。在大细胞神经分泌核中发现标记程度较轻的细胞,包括室旁核和室旁核嘴侧部分的外侧部分、视上核和附属大细胞核。除了腹内侧下丘脑核后部的少数轻度标记细胞外,在腹内侧下丘脑核中未发现逆行标记的细胞。然而,如果注入的示踪剂扩散到弓状核,则整个腹内侧核中都有标记细胞。在下丘脑的其他部分,包括视前区的外侧和后部、下丘脑前区和视交叉上核,或中脑、脑桥和延髓的儿茶酚胺能细胞群中未发现标记细胞。将HRP对照注射到垂体后叶和腹内侧核中产生的细胞标记模式与注入正中隆起时所见的模式非常不同。注入垂体后叶后,大细胞神经分泌核的细胞全部被大量标记,但小细胞神经元群中的小细胞未被标记。直接注入腹内侧核导致下丘脑广泛区域的细胞被标记,以及终纹床核和外侧隔、杏仁复合体和海马下托的部分区域,以及中脑、脑桥和延髓的几个细胞群被标记。