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H Schnyder

Publications and source records attributed to H Schnyder.

22 records · Page 2Linked to original sources

The isthmus-tegmentum complex in the turtle and rat: a comparative analysis of its interconnections with the optic tectum.

Injections of horseradish peroxidase, wheat germ agglutinin and various amino acids into the optic tectum in both the turtle and rat, and into the nucleus isthmi magnocellularis (IsM) in the turtle were used to analyse the connections of the isthmus-tegmentum complex. The connectivities and the selective retrograde transport properties in certain tectal pathways were taken as a basis to define more accurately isthmus-tegmentum complex subdivisions. There were several main findings. In the turtle the projection from the tectum to the IsM originated in the stratum griseum periventriculare, whereas the projection from the IsM to the tectum terminated in the superficial tectal layers (both projections homolateral). The terminations of the pathway from IsM to tectum were not uniformly distributed throughout the tectal surface; rather, alternating zones of high and low termination density along the lateral dimension were observed. The turtle nucleus isthmi parvocellularis, receiving a few tectal fibers and afferents from the ipsilateral IsM, gave rise to a bilateral tectal projection. Evidence was obtained for a crossed collicular projection to the rat parabigeminal nucleus (Pbg) in addition to the established uncrossed one. GABA was retrogradely transported from the optic tectum to the Pbg in the rat, and to the dorsolateral mesencephalic tegmentum and the IsM in the turtle. After glycine injections into the optic tectum, the dorsomedial peri-parabigeminal tegmentum was retrogradely labeled in the rat, and the IsM in the turtle. An attempt was made to outline the parallelism between the organizations of the isthmus-tegmentum complexes in the turtle, pigeon and rat. It was concluded that some basic features in the inter-connectivity of the isthmus-tegmentum complex and other parts of the visual system have been preserved in evolution, despite the apparent loss of the isthmo-retinal projection in mammals.

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The retinopetal system in the turtle Pseudemys scripta elegans.

Injections of 125I wheat-germ agglutinin or horseradish peroxidase into the eyes of turtles labeled retrogradely cells in a mesencephalic reticular area lying between the trochlear and the isthmic nuclei. Their number was small and they were found predominantly contralateral to the injected eye. These reticular neurons were not labeled following control injections into the orbital cavity and therefore are considered to project to the retina similar to correspondingly located neurons in some other vertebrates.

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Do retinal and spinal projections overlap within the turtle thalamus?

The spinal and retinal projections to the turtle thalamus were studied using the autoradiographic tracing technique. Particular attention is given to the regions receiving both spinal and retinal projections: the ovalis complex and a perirotundal stripe. Spinal and retinal projections do not overlap significantly in either of these regions. In the perirotundal stripe there appears to be little likelihood of convergence of these projections on single neurons. In the ovalis complex, the most densely and the most consistently innervated thalamic region, however, the respective spinal and retinal target areas are located immediately adjacent to each other and low order somatosensory and visual projections may converge on single neurons with dendrites extending into both the spinal and retinal terminal arborizations. The ovalis complex in the turtle may be compared with the ventral part of the mammalian lateral geniculate nucleus. Both these nuclei receive spinal and retinal projections and both, reportedly, do not project to the telencephalon. The findings are discussed in relation to the possible evolution of the specific thalamic sensory nuclei in higher mammals as well as to the prosencephalic processing of somatosensory and visual information in turtles and mammals.

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