Jakubowska-Sadowska K, Moryś J, Sadowski M, Kowiański P, Karwacki Z, Narkiewicz O
Department of Anatomy and Neurobiology, Medical University of Gdańsk, Poland.
Anat Embryol (Berl). 1998 Jul;198(1):63-72. doi: 10.1007/s004290050165.
The retrograde axonal transport method was used to compare the topography and organization of the visual zone of the claustrum in rat, guinea pig, rabbit and cat. First, massive Fluoro-Gold injections were placed into the primary visual cortex and the secondary areas. Experiments showed differences in the location of the visual zone among the animals under study. In rat, the visual zone occupied the posteroventral part of the claustrum and spread to its anterior pole. In guinea pig, neurons projecting to the visual cortex were located dorsally in the posterior half of the claustrum. In rabbit, similarly to the rat, they were localized in the posteroventral part; however, they did not reach the anterior pole. In cat, neurons that project to the visual cortex were concentrated dorsally in the posterior fourth of the claustrum. In double-injection experiments, Fast Blue and Diamidino Yellow were placed into the primary and secondary visual areas in various combinations. The experiments showed that in the rat and the rabbit claustral neurons project to primary visual cortex (area 17) as well as to both secondary visual areas (areas 18a and b). Populations of neurons sending axons to the primary and secondary areas showed full overlap. The presence of double-labeled neurons indicates that some claustral neurons project both to the primary and secondary fields. In cat, neurons that project to the primary visual cortex appear to be clearly separated from those connected with the secondary visual area, as no double-labeled neurons were found. In all studied species, the double injections placed into the visual and primary somatosensory cortex did not result in any double-labeling neurons. Our results indicate that the location of the visual zone in the posterior part of the claustrum is a phylogenetically stable feature, whereas its dorsoventral shift as well as the extent toward the anterior pole is related to the particular species. The overlap of neurons projecting to the primary and secondary visual areas in the rat and rabbit as well as the separation of both projections in cat appear to reflect the higher degree of complexity of the visual system in the latter.
采用逆行轴突运输法比较大鼠、豚鼠、兔和猫屏状核视觉区的局部解剖结构和组织。首先,将大量荧光金注入初级视皮层和次级视区。实验显示,在所研究的动物中,视觉区的位置存在差异。在大鼠中,视觉区占据屏状核的后腹部分,并延伸至其前极。在豚鼠中,投射至视皮层的神经元位于屏状核后半部的背侧。在兔中,与大鼠类似,它们位于后腹部分;然而,它们并未到达前极。在猫中,投射至视皮层的神经元集中在屏状核后四分之一的背侧。在双注射实验中,将快蓝和双脒基黄以各种组合注入初级和次级视区。实验表明,在大鼠和兔中,屏状核神经元投射至初级视皮层(17区)以及两个次级视区(18a和18b区)。向初级和次级视区发送轴突的神经元群体完全重叠。双标记神经元的存在表明,一些屏状核神经元既投射至初级视区也投射至次级视区。在猫中,投射至初级视皮层的神经元似乎与那些连接次级视区的神经元明显分开,因为未发现双标记神经元。在所有研究的物种中,将双注射剂注入视皮层和初级体感皮层均未产生任何双标记神经元。我们的结果表明,屏状核后部视觉区的位置是一个系统发育上稳定的特征,而其背腹移位以及向前极的延伸程度与特定物种有关。大鼠和兔中投射至初级和次级视区的神经元重叠以及猫中两种投射的分离似乎反映了后者视觉系统更高程度的复杂性。