Saunders Richard C, Aggleton John P
Laboratory of Neuropsychology, National Institute of Mental Health, Bethesda, Maryland 20892, USA.
Hippocampus. 2007;17(5):396-411. doi: 10.1002/hipo.20276.
The distribution of neurons contributing to the fornix was mapped by placing the retrograde tracer horseradish peroxidase (HRP) in polyacrylamide gels in different medial to lateral locations within the fornix of three rhesus monkeys (Macaca mulatta). The HRP was placed from 3 to 5 mm caudal to the descending columns of the fornix. Additional information came from a series of rhesus and cynomolgus monkeys (Macaca fasciculata) with anterograde tracer injections in the medial temporal lobe. The hippocampal formation, including the subiculum and presubiculum, together with the entorhinal cortex (EC) and perirhinal cortex (area 35) contribute numerous axons to the fornix in a topographical manner. In contrast, the lateral perirhinal cortex (area 36) and parahippocampal cortical areas TF and TH only contained a handful of cells labeled via the fornix. The medial fornix originates from cells in the caudal half of the subiculum, the lamina principalis interna of the caudal half of the presubiculum, and from the perirhinal cortex (area 35). The intermediate portion of the fornix (i.e., that part midway between the midline and most lateral parts of the fornix) originates from cells in the rostral half of the subiculum and prosubiculum, the anterior presubiculum (only from the lamina principalis externa), the caudal presubiculum (primarily from lamina principalis interna), the rostral half of CA3, the EC (primarily 28I and 28M), and the perirhinal cortex (area 35). The lateral parts of the fornix arise from the rostral EC (28L only) and the most rostral portion of CA3. Subcortically, the medial septum, nucleus of the diagonal band, supramammillary nucleus, lateral hypothalamus, dorsal raphe nucleus, and the thalamic nucleus reuniens all send projections through the fornix, which presumably terminate in the hippocampus and adjacent parahippocampal region. These results not only help to define those regions that project via the fornix, but also reveal those subcortical projections to the hippocampal formation most likely to rely entirely on nonfornical pathways.
通过将逆行示踪剂辣根过氧化物酶(HRP)置于三只恒河猴(猕猴)穹窿内从内侧到外侧不同位置的聚丙烯酰胺凝胶中,绘制了对穹窿有贡献的神经元分布。HRP被放置在穹窿下行柱尾侧3至5毫米处。另外的信息来自一系列在内侧颞叶注射顺行示踪剂的恒河猴和食蟹猴(束毛猕猴)。海马结构,包括下托和前下托,连同内嗅皮质(EC)和嗅周皮质(35区)以拓扑方式向穹窿贡献大量轴突。相比之下,外侧嗅周皮质(36区)以及海马旁皮质区TF和TH仅含有少数经穹窿标记的细胞。内侧穹窿起源于下托后半部的细胞、前下托后半部的内主层,以及嗅周皮质(35区)。穹窿的中间部分(即穹窿中线与最外侧部分之间的中间部分)起源于下托和前下托的前半部细胞、前下托(仅来自外主层)、后下托(主要来自内主层)、CA3的前半部、EC(主要是28I和28M),以及嗅周皮质(35区)。穹窿的外侧部分起源于前EC(仅28L)和CA3的最前部。在皮质下,内侧隔核、斜角带核、乳头体上核、外侧下丘脑、背侧中缝核和丘脑连合核均通过穹窿发出投射,这些投射可能终止于海马和相邻的海马旁区域。这些结果不仅有助于确定通过穹窿投射的区域,还揭示了那些最有可能完全依赖非穹窿途径投射到海马结构的皮质下投射。