Newman A, Suárez C, Lee W S, Honrubia V
Division of Head and Neck Surgery, UCLA School of Medicine 90024-1624.
Brain Res. 1992 Dec 4;597(2):278-97. doi: 10.1016/0006-8993(92)91485-w.
The morphological characteristics of the vestibular nuclei of the chinchilla were studied in horizontally cut serial sections of the brain stem. Horseradish peroxidase labeling allowed unambiguous delineation of the vestibular nuclei and areas of innervation by the vestibular afferent fibers. The cytoarchitecture of the vestibular nuclei was documented with the aid of camera lucida drawings and quantitatively evaluated with computerized methodology. The cellular groups identified in other species were found in the chinchilla. The superior vestibular nucleus (SN) originated ventromedial to the mesencephalic tract and nuclei of the trigeminal nerve. This nucleus contained medium-sized cells with a central group of larger cells (20-34 microns in diameter). It received its maximum vestibular innervation caudally in the ventrolateral and dorsal aspects of the nucleus. Fibers projected to the SN in bundles with thick fibers surrounded by thin ones. The lateral vestibular nucleus (LN) originated 0.9-1.2 mm below the rostral aspect of the vestibular area. It was ventrocaudal to the SN and contained many large cells with diameters of 45-60 microns. The LN was innervated mainly in the ventrocaudal aspect by oblique and transverse fibers that formed a dense mesh. The medial vestibular nucleus (MN) originated 0.3-0.6 mm caudal to the beginning of the SN, adjacent to the floor of the IVth ventricle. It extended for 3-4 mm along the SN, LN and descending vestibular nucleus (DN). The MN contained the densest and most homogeneous cells, which had diameters of 10-20 microns. This nucleus received its greatest innervation at the level of the vestibular root. Thin fibers traveled to the MN through the SN and LN. The caudal pole of the nucleus did not receive fibers. The DN originated 1.8-2.5 mm caudal to the origination of the SN, between the caudal LN and the MN. Caudally it replaced the LN. Most of the cells of the DVN were medium-sized, with diameters of 10-20 microns. The main vestibular innervation of the DN was in the lateral aspect of the nucleus. Tertiary fibers projected in small, separate bundles of uniform-sized thick fibers. The interstitial nucleus originated 1.1-1.4 mm from the beginning of the SN. It occupied the center of the vestibular root, 0.8-0.9 mm medial to the root entry zone. It contained a few large cells (greater than 20 microns in diameter), many medium-sized cells, and some small cells.(ABSTRACT TRUNCATED AT 400 WORDS)
在脑干水平切片中研究了龙猫前庭核的形态学特征。辣根过氧化物酶标记使得前庭核和前庭传入纤维的神经支配区域得以明确界定。借助于明视绘图记录前庭核的细胞结构,并采用计算机方法进行定量评估。在龙猫中发现了在其他物种中所识别出的细胞群。上前庭核(SN)起源于中脑导水管周围灰质腹内侧和三叉神经核。该核包含中等大小的细胞以及中央一组较大的细胞(直径为20 - 34微米)。它在核的尾侧腹外侧和背侧接受最大程度的前庭神经支配。纤维成束投射至SN,厚纤维被薄纤维环绕。外侧前庭核(LN)起源于前庭区嘴侧端下方0.9 - 1.2毫米处。它位于SN的腹尾侧,包含许多直径为45 - 60微米的大细胞。LN主要在腹尾侧接受由斜行和横行纤维形成致密网状结构的神经支配。内侧前庭核(MN)起源于SN起始部尾侧0.3 - 0.6毫米处,毗邻第四脑室底。它沿着SN、LN和降前庭核(DN)延伸3 - 4毫米。MN包含最密集且最均匀的细胞,其直径为10 - 20微米。该核在前庭根水平接受最丰富的神经支配。细纤维通过SN和LN到达MN。核的尾极不接受纤维。DN起源于SN起始部尾侧1.8 - 2.5毫米处,位于尾侧LN和MN之间。在尾侧它取代了LN。DN的大多数细胞为中等大小,直径为10 - 20微米。DN的主要前庭神经支配位于核的外侧。三级纤维以小的、单独的、大小均匀的厚纤维束投射。间质核起源于距SN起始部1.1 - 1.4毫米处。它占据前庭根的中心,在根进入区内侧0.8 - 0.9毫米处。它包含一些大细胞(直径大于20微米)、许多中等大小的细胞和一些小细胞。(摘要截断于400字)