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Pre‐ and postmetamorphic organization of the vestibular nuclear complex in the turbot examined by retrograde tracer substances
Author(s) -
Jansen J.K.S.,
Enger P.S.
Publication year - 1996
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/(sici)1096-9861(19960122)364:4<677::aid-cne6>3.0.co;2-0
Subject(s) - vestibular nuclei , vestibular system , anatomy , biology , metamorphosis , vestibulo–ocular reflex , neuroscience , oculomotor nucleus , saccule , spinal cord , medial longitudinal fasciculus , central nervous system , midbrain , larva , botany
During metamorphosis of flatfish larvae, eye migration leads to a 90° misalignment of the visual and vestibular frames of reference. In order to maintain vestibular eye stabilization, the vestibulo‐ocular (V‐O) pathways have to be radically reorganized. Here, we have examined the vestibular projections in turbot larvae and juveniles by means of conventional neurohistological techniques using horseradish peroxidase and fluorescent dextranamines as tracers. We have found that the vestibular projections to the rostral eye motor nuclei consist of five densely clustered groups of neurons projecting to the rostral eye motor nuclei, some through the ipsilateral, others through the contralateral medial longitudinal fascicle (MLF). In addition, there are three groups of vestibulo‐spinal neurons. The most prominent of these gives rise to the ipsilateral vestibulo‐spinal tract. The other two project contralaterally, one descending in the MLF, the other more laterally in the anterior funiculus of the spinal cord. These subnuclei of the vestibular complex are easily identifiable in larvae before metamorphosis, as well as in juvenile turbots. The number of projection neurons in each of the subnuclei is approximately doubled over the period of metamorphosis. Applying different tracers to rostrally and caudally projecting pathways, we found no double‐labeled neurons, indicating that the V‐O and vestibulo‐spinal groups are distinct entities. However, by applying the two tracers ipsi‐and contralaterally in the terminal fields in the rostral eye motor nuclei after metamorphosis, we found many double‐labeled neurons in all the V‐O subgroups. In contrast, we found only a small fraction of double‐labeled vestibular neurons when the same strategy was applied to larval preparations. We conclude that 1) the basic organization of the vestibular nuclei of the turbot is similar to that of other teleosts, in larvae as well as juveniles; 2) there is a substantial increase in projection neurons over the period of metamorphosis in all the subgroups of the vestibular nuclear complex; and 3) many more of the V‐O neurons project bilaterally to the rostral eye motor nuclei in juvenile than in larval turbots. © 1996 Wiley‐Liss, Inc.