Akbarian S, Grüsser O J, Guldin W O
Department of Physiology, Freie Universität Berlin, Germany.
J Comp Neurol. 1993 Jun 1;332(1):89-104. doi: 10.1002/cne.903320107.
Single- and multiple-unit recordings were made from nerve cells located in the different nuclei of the brainstem vestibular nuclear complex (VNC) of anaesthetized squirrel monkeys (Saimiri sciureus) by conventional stereotaxic techniques. After neurons responding to semicircular canal stimulation in a yaw, roll, or pitch direction or to otholith stimulation were identified, small amounts of retrograde tracer substances were deposited at the recording sites. Up to three different tracers were administered to different parts of the VNC in the same animal (Fast Blue, HRP-WGA, and Rhodamine-dextranes). After adequate survival times, the animals were sacrificed. Following histological processing, the cortical grey matter was screened systematically for cells labelled with the retrograde tracers (fluorescence microscopy or light microscopy for HRP processing). Labelled nerve cells which clearly project to the VNC directly were found predominantly in the cytoarchitectonic layer 5 of seven different cortical areas: 1) The parieto-insular vestibular cortex PIVC, which in squirrel monkeys consists mainly of the medial area Ri and parts of the anterior area Ig; 2) area 7ant, which presumably corresponds to the macaque area 2v; 3) area 3aV, a vestibular field of area 3a; 4) the temporal area T3 bordering on area Ri; 5) the premotor area 6a; and 6, 7) the areas 6c and 23c of the anterior cingulate cortex. The PIVC, area 7ant, and area 3aV form the "inner cortical vestibular circuit" (Guldin et al.: J. Comp. Neurol. 326:375-401, '92), while the other cortical areas mentioned also have direct projections to the structures of the inner cortical vestibular circuit. It is speculated that the direct projections of the cortical vestibular structures to the brainstem vestibular nuclei regulate the vestibulo-ocular, the vestibulo-spinal, and the optokinetic reflexes mediated through the VNC, thus preventing counteractions of these reflexes during voluntary, goal-directed head movements or locomotion.
采用传统的立体定位技术,从麻醉的松鼠猴(松鼠猴属)脑干前庭核复合体(VNC)不同核团中的神经细胞进行单单位和多单位记录。在识别出对偏航、横滚或俯仰方向的半规管刺激或耳石刺激有反应的神经元后,将少量逆行示踪剂物质沉积在记录部位。在同一动物的VNC不同部位给予多达三种不同的示踪剂(快蓝、HRP-WGA和罗丹明葡聚糖)。经过适当的存活时间后,处死动物。经过组织学处理后,系统地在皮质灰质中筛选用逆行示踪剂标记的细胞(荧光显微镜或用于HRP处理的光学显微镜)。直接投射到VNC的标记神经细胞主要存在于七个不同皮质区域的细胞构筑第5层:1)顶岛前庭皮质PIVC,在松鼠猴中主要由内侧区域Ri和前部区域Ig的部分组成;2)7ant区,可能对应于猕猴的2v区;3)3aV区,3a区的前庭场;4)与Ri区相邻的颞区T3;(5)运动前区6a;以及6、7)前扣带回皮质的6c区和23c区。PIVC、7ant区和3aV区形成“皮质内前庭回路”(Guldin等人:《比较神经学杂志》326:375 - 401,'92),而提到的其他皮质区域也直接投射到皮质内前庭回路的结构。据推测,皮质前庭结构向脑干前庭核的直接投射调节通过VNC介导的前庭眼反射、前庭脊髓反射和视动反射,从而在自愿的、有目标的头部运动或运动过程中防止这些反射的对抗作用。