Záborszky L, Carlsen J, Brashear H R, Heimer L
J Comp Neurol. 1986 Jan 22;243(4):488-509. doi: 10.1002/cne.902430405.
We have examined the location of cholinergic and GABAergic neurons that project to the rat main olfactory bulb by combining choline acetyltransferase (ChAT) and glutamic acid decarboxylase (GAD) immunohistochemistry with retrograde fluorescent tracing. Since many of the projection neurons are located in subcortical basal forebrain structures, where the delineation of individual regions is difficult, particular care was taken to localize projection neurons with respect to such landmarks as the ventral pallidum (identified on the basis of GAD immunoreactivity), the diagonal band, and medial forebrain bundle. In addition, sections with fluorescent tracers or immunofluorescence were counterstained for Nissl substance in order to correlate tracer or immunopositive neurons with the cytoarchitecture of the basal forebrain. The majority of the cholinergic bulbopetal neurons are located in the medial half of the nucleus of the horizontal limb of the diagonal band (HDB), whereas only a few are located in its lateral half. A substantial number of cholinergic bulbopetal cells are also found in the sublenticular substantia innominata. A small number of cholinergic bulbopetal neurons, finally, are located in the ventrolateral portion of the nucleus of the vertical limb of the diagonal band. At the level of the crossing of the anterior commissure, approximately 17% of the bulbopetal neurons in the HDB are ChAT-positive. The noncholinergic bulbopetal cells are located mainly in the lateral half of the HDB. GAD-containing bulbopetal neurons are primarily located in the caudal part of the HDB, especially in its lateral part. About 30% of the bulbopetal projection neurons in the HDB are GAD-positive. A few GAD-positive bulbopetal cells, furthermore, are located in the ventral pallidum, anterior amygdaloid area, deep olfactory cortex, nucleus of the lateral olfactory tract, lateral hypothalamic area, and tuberomamillary nucleus. The topography of bulbopetal neurons was compared to other projection neurons in the HDB. After multiple injections of fluorescent tracer in the neocortex, retrogradely labeled neurons were concentrated in the most medial part of the HDB, while neurons projecting to the olfactory and entorhinal cortices were located in the ventral part of the HDB. These results show that the cells of the HDB can be divided into subpopulations based upon projection target as well as transmitter content. Furthermore, these subpopulations correspond, at least to a considerable extent, to areas that can be defined on cyto- and fibroarchitectural grounds.
我们通过将胆碱乙酰转移酶(ChAT)和谷氨酸脱羧酶(GAD)免疫组织化学与逆行荧光追踪相结合,研究了投射到大鼠主嗅球的胆碱能和GABA能神经元的位置。由于许多投射神经元位于皮质下基底前脑结构中,而这些结构中各个区域的划分较为困难,因此在确定投射神经元相对于腹侧苍白球(根据GAD免疫反应性确定)、斜角带和内侧前脑束等标志物的位置时格外小心。此外,对含有荧光示踪剂或免疫荧光的切片进行尼氏物质复染,以便将示踪剂或免疫阳性神经元与基底前脑的细胞结构相关联。大多数胆碱能向嗅球投射的神经元位于斜角带水平支核(HDB)的内侧半部分,而只有少数位于其外侧半部分。在豆状核下无名质中也发现了大量胆碱能向嗅球投射的细胞。最后,少数胆碱能向嗅球投射的神经元位于斜角带垂直支核的腹外侧部分。在前连合交叉水平,HDB中约17%的向嗅球投射的神经元为ChAT阳性。非胆碱能向嗅球投射的细胞主要位于HDB的外侧半部分。含GAD的向嗅球投射神经元主要位于HDB的尾部,尤其是其外侧部分。HDB中约30%的向嗅球投射神经元为GAD阳性。此外,少数GAD阳性的向嗅球投射细胞位于腹侧苍白球、杏仁前区、深部嗅皮质、外侧嗅束核、外侧下丘脑区和乳头体核。将向嗅球投射神经元的拓扑结构与HDB中的其他投射神经元进行了比较。在新皮质多次注射荧光示踪剂后,逆行标记的神经元集中在HDB最内侧部分,而投射到嗅皮质和内嗅皮质的神经元位于HDB的腹侧部分。这些结果表明,HDB的细胞可以根据投射靶点以及神经递质含量分为不同的亚群。此外,这些亚群至少在很大程度上对应于可以根据细胞结构和纤维结构定义的区域。