Literature DB >> 1083857

Topological analysis of the brain stem of the frogs Rana esculenta and Rana catesbeiana.

R Opdam, M Kemali, R Nieuwenhuys.   

Abstract

The ventricular sulcal pattern and the cytoarchitectonic organization of the brain stem of the frogs Rana esculenta and Rana catesbeiana have been studied in transversely cut, Nissl stained serial sections. Four longitudinal sulci, the sulcus medianus inferior, the sulcus intermedius ventralis, the sulcus limitans and the sulcus medianus superior could be distinguished in both species. A fifth longitudinal groove, the sulcus intermedius dorsalis, was found only in Rana esculenta. With the aid of the usual cytoarchitectonic criteria 25 cell masses have been delineated in Rana esculenta and 27 in Rana catesbeiana. These cell masses can be distributed over the following categories (numbers added in brackets for Rana catesbeiana, if different from those in Rana esculenta): primary efferent or motor, 8; primary afferent or sensory, 4(6); "relay" centers, 7. Contrary to statements in the literature the reticular formation can be divided into six separate cell groups. The majority of the nuclei form part of the central gray, which constitutes a rather wide zone in anurans; three reticular nuclei lie partly within the stratum griseum and partly within the stratum album; six nuclei are entirely embedded in the stratum album. The morphological pattern of the cell masses and their relationship to the ventricular sulci were studied with the aid of a graphical reconstruction procedure termed topological analysis (cf. Nieuwenhuys, '74 and figs. 15, 16). This analysis yielded the following results: The sulcus limitans extends throughout the rhombencephalon, dividing this brain part into a basal plate and an alar plate. The cell masses in the basal plate fit into two longitudinal zones, a medial area ventralis and a lateral area intermedioventralis. The area ventralis contains three somatic motor nuclei (IV, VI and XII) and the rhombencephalic medial reticular zone. The latter may be primarily considered as a somatic motor coordinating center. The area intermedioventralis contains the visceral motor nuclei of V, VII, IX and X. However, the basal plate also contains a number of non-motor centers, for example the superior olive. The alar plate contains visceral sensory, general somatic sensory and special somatic sensory centers. Two cell masses, the nucleusfasciculi solitarii and the nucleus visceralis secundarius, represent together a discontinuous visceral sensory zone. Both of these nuclei are situated immediately dorsal to the sulcus limitans. The special somatic sensory area, i.e., the area of termination of the eighth nerve, occupies a considerable part of the alar plate. This area comprises, apart from a large zone of diffuse gray, three distinct cell masses...

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Year:  1976        PMID: 1083857     DOI: 10.1002/cne.901650304

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  12 in total

1.  Developmental and regional patterns of GAP-43 immunoreactivity in a metamorphosing brain.

Authors:  Andrea Megela Simmons; Leslie H Tanyu; Seth S Horowitz; Judith A Chapman; Rebecca A Brown
Journal:  Brain Behav Evol       Date:  2008-04-21       Impact factor: 1.808

2.  The organization of descending tectofugal pathways underlying orienting in the frog, Rana pipiens. II. Evidence for the involvement of a tecto-tegmento-spinal pathway.

Authors:  T Masino; P Grobstein
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

3.  Plasticity of auditory medullary-midbrain connectivity across metamorphic development in the bullfrog, Rana catesbeiana.

Authors:  Seth S Horowitz; Judith A Chapman; Andrea Megela Simmons
Journal:  Brain Behav Evol       Date:  2006-08-14       Impact factor: 1.808

4.  Observations on the development of cerebellar afferents in Xenopus laevis.

Authors:  J A van der Linden; H J ten Donkelaar
Journal:  Anat Embryol (Berl)       Date:  1987

5.  Cerebellar afferents in the frogs, Rana esculenta and Rana temporaria.

Authors:  B G Grover; U Grüsser-Cornehls
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

6.  [The origin of efferent fibers to the inner ear on reptiles. A HRP study in Caiman crocodilus (author's transl)].

Authors:  J Strutz; C Beck; C L Schmidt
Journal:  Arch Otorhinolaryngol       Date:  1981

7.  Immunohistochemical demonstration of the serotonin neuron system in the central nervous system of the bullfrog, Rana catesbeiana.

Authors:  S Ueda; Y Nojyo; Y Sano
Journal:  Anat Embryol (Berl)       Date:  1984

8.  Location of efferent neurons to the labyrinth of the green tree frog (Hyla cinerea). A horseradish peroxidase study.

Authors:  J Strutz; K Bielenberg; W B Spatz
Journal:  Arch Otorhinolaryngol       Date:  1982

9.  Growth patterns in the lateral wall of the mouse telencephalon. II. Histological changes during and subsequent to the period of isocortical neuron production.

Authors:  I H Smart; G M McSherry
Journal:  J Anat       Date:  1982-05       Impact factor: 2.610

10.  Dynamic visualization of the developing nervous system of the bullfrog, Rana catesbeiana.

Authors:  Seth S Horowitz; Andrea Megela Simmons
Journal:  Brain Res       Date:  2007-05-06       Impact factor: 3.252

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