Sas E, Maler L, Weld M
University of Ottawa, Faculty of Medicine, Department of Anatomy and Neurobiology, Ontario, Canada.
J Comp Neurol. 1993 Sep 22;335(4):486-507. doi: 10.1002/cne.903350403.
This work examines the connectivity of the olfactory bulb in the gynmotiform fish Apteronotus leptorhynchus. Wheat germ agglutinin conjugated horseradish peroxidase was iontophoresed in different areas and depths of the bulb in order to define its efferent and afferent connections. The olfactory bulb projects bilaterally via the medial (medial and centromedial fascicles) and lateral olfactory (lateral and centrolateral fascicles) tracts. The nervus terminalis courses through the ventromedial aspect of the bulb to terminate in parts of the medial subpallium and hypothalamus. Its telencephalic component could be identified by a nonpreadsorbable substance P-like immunoreactivity. Fibers within the medial olfactory tract form four telencephalic terminal fields: peduncular, medial, intermediate and posterior fields. The diencephalic terminal fields in the habenula, preoptic, and hypothalamic areas appear to correspond to some of the nervus terminalis fibers (von Bartheld and Meyer [1986] Cell Tissue Res. 245:143-158, Krishna et al. [1992] Gen. Comp. Endocrinol. 85:111-117), and to axons of telencephalic bulbopetal cells of area dorsalis posterior. The terminal fields of the medial olfactory tract and nervus terminalis partially overlap in the ventral telencephalic areas partes ventralis, supracommissuralis, and rostral preoptic region. The lateral olfactory tract forms a lateral terminal field and contributes to the intermediate and posterior terminal fields. Olfactory fibers cross in the interbulbar, anterior, and habenular commissures and tuberal decussation. Consistent differences were noted between the medial and lateral olfactory bulb, with respect to their cytoarchitectonics, immunohistochemistry, and connections. In addition to the olfactory nerve, bulbar afferents are predominantly ipsilateral, with minor inputs originating from the contralateral bulb and telencephalic area dorsalis posterior, nucleus raphe centralis, and locus ceruleus.
本研究探讨了裸背电鳗(Apteronotus leptorhynchus)嗅球的连接情况。将小麦胚芽凝集素结合辣根过氧化物酶通过离子电泳法注入嗅球的不同区域和深度,以确定其传出和传入连接。嗅球通过内侧(内侧和中央内侧束)和外侧嗅束(外侧和中央外侧束)向双侧投射。终神经穿过嗅球腹内侧部分,终止于内侧皮质下区和下丘脑的部分区域。其端脑成分可通过一种不可吸收的P物质样免疫反应性来识别。内侧嗅束内的纤维形成四个端脑终末场:脚区、内侧区、中间区和后区。缰核、视前区和下丘脑区的间脑终末场似乎与一些终神经纤维相对应(冯·巴特霍尔德和迈耶[1986]《细胞与组织研究》245:143 - 158,克里希纳等人[1992]《普通与比较内分泌学》85:111 - 117),也与背侧后区端脑嗅球向心性细胞的轴突相对应。内侧嗅束和终神经的终末场在腹侧端脑区域腹侧部、连合上部和视前区前部部分重叠。外侧嗅束形成一个外侧终末场,并对中间和后终末场有贡献。嗅纤维在球间、前和缰连合以及结节交叉处交叉。在内侧和外侧嗅球之间,在细胞结构、免疫组织化学和连接方面存在一致的差异。除了嗅神经外,嗅球传入纤维主要是同侧的,少数输入来自对侧嗅球、端脑背侧后区、中缝中央核和蓝斑核。