Barry M A
School of Life and Health Sciences, University of Delaware, Newark 19711.
J Comp Neurol. 1987 Dec 22;266(4):457-77. doi: 10.1002/cne.902660403.
Horseradish peroxidase techniques were employed to trace the central projections of afferents from the individual endorgans of the membranous labyrinth and to delineate the efferent projections from the primary octaval nuclei to the spinal cord and midbrain octavolateralis area in the clearnose skate, Raja eglanteria. First-order octaval afferents project ipsilaterally to five primary octaval nuclei, namely: magnocellular, descending, posterior, anterior, and periventricular. Octaval afferents also terminate in the reticular formation, nucleus intermedius (primary mechanoreceptive lateral-line nucleus), and vestibulolateral lobe of the cerebellum. Each primary octaval nucleus receives afferent input from each labyrinthine endorgan, with the possible exception of macula neglecta input to the magnacellular nucleus. Within the anterior, descending, and to a lesser extent posterior and magnocellular nuclei, this input is largely nonoverlapping. Semicircular canal cristae afferents terminate ventrally, saccular and lagenar afferents dorsally, utricular afferents laterally, and macular neglecta afferents course ventrally but terminate largely dorsally within these nuclei. In the vestibulolateral lobe of the cerebellum, cristae afferents project primarily to the pars medialis, whereas macular endorgan afferents terminate in the pars lateralis. Primary afferent input to the reticular formation is predominantly from the horizontal canal crista. The densest projections to nucleus intermedius are from the utriculus and sacculus. Vestibulospinal projections originate primarily from the magnocellular and descending nuclei. Second-order auditory neurons are most likely located in dorsomedial parts of the descending and anterior nuclei. Cells in these nuclei project directly to the auditory area of the midbrain octavolateralis complex, but projections to this area originate predominantly from nuclei C1 and C2, which are possible superior olivary homologues.
采用辣根过氧化物酶技术追踪了膜迷路各终器传入纤维的中枢投射,并描绘了在星点鳐(Raja eglanteria)中从初级听神经核到脊髓和中脑听外侧区的传出投射。一级听神经传入纤维同侧投射到五个初级听神经核,即:大细胞核、下行核、后核、前核和室周核。听神经传入纤维也终止于网状结构、中间核(初级机械感受性侧线核)和小脑的前庭外侧叶。每个初级听神经核接收来自每个迷路终器的传入输入,但大细胞核可能除外,其可能不接收忽视斑的输入。在前核、下行核以及程度稍轻的后核和大细胞核内,这种输入在很大程度上不重叠。半规管嵴传入纤维终止于腹侧,球囊和瓶状囊传入纤维终止于背侧,椭圆囊传入纤维终止于外侧,而忽视斑传入纤维走行于腹侧,但在这些核内主要终止于背侧。在小脑的前庭外侧叶,嵴传入纤维主要投射到内侧部,而斑状终器传入纤维终止于外侧部。对网状结构的初级传入输入主要来自水平半规管嵴。对中间核的最密集投射来自椭圆囊和球囊。前庭脊髓投射主要起源于大细胞核和下行核。二级听觉神经元很可能位于下行核和前核的背内侧部分。这些核内的细胞直接投射到中脑听外侧复合体的听觉区,但对该区域的投射主要起源于C1和C2核,它们可能是上橄榄核的同源物。