Literature DB >> 6163797

Distribution of dendrites from biventer cervicis and complexus motoneurons stained intracellularly with horseradish peroxidase in the adult cat.

P K Rose.   

Abstract

The three-dimensional distribution of dendrites from the dorsal neck muscles biventer cervicis (BC) and complexus (CM) was examined in the adult cat using intracellular staining techniques. Motoneurons were electrophysiologically identified, stained with injection of horseradish peroxidase, and reconstructed from serial histological sections. The dendritic distributions of all motoneurons examined followed an orderly pattern. Many dendrites extended rostrally and caudally to form of complex parallel collection of dendrites in the ventromedial nucleus. Other dendrites projected dorsolaterally into the spinal accessory nucleus and lateral parts of lamina VII and VIII. Dorsomedial dendrites followed a path parallel to the medial border of the ventral horn are frequently terminated near the central canal. A new scattered dendrites were usually found directly dorsal to the soma in lamina VIII. This pattern of dendritic distribution differed distinctly from the dendritic distribution of motoneurons in other spinal regions. However, in all spinal regions, including the upper cervical spinal cord where BC and CM motoneurons were found, the pattern of dendritic distribution from different motoneurons was similar if their somata were located in the same region. For 15 motoneurons with well-stained dendrites, the mean rostral-caudal extent of the dendritic tree was 2,860 micrometers. The mean total dendritic length of three of these motoneurons measured 73,100 micrometers, almost four times larger than hindlimb motoneurons involved in planter reflexes. Despite the large size of the dendritic trees of BC and CM motoneurons, the surface areas of BC and CM cell bodies were smaller than most large hindlimb motoneurons. These quantitative differences in motoneuron dimensions may in turn be reflected by differences in the electrotonic properties of motoneurons in different motoneuron nuclei.

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Year:  1981        PMID: 6163797     DOI: 10.1002/cne.901970304

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


  13 in total

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Journal:  Anat Rec (Hoboken)       Date:  2008-02       Impact factor: 2.064

2.  Integration in descending motor pathways controlling the forelimb in the cat. 18. Morphology, axonal projection and termination of collaterals from C3-C4 propriospinal neurones in the segment of origin.

Authors:  B Alstermark; T Isa; B Tantisira
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  Light microscopical study of dendrites and perikarya of interneurones mediating la reciprocal inhibition of cat lumbar alpha-motoneurones.

Authors:  J Rastad; P Gad; E Jankowska; D McCrea; J Westman
Journal:  Anat Embryol (Berl)       Date:  1990

4.  Projections from the rostral mesencephalic reticular formation to the spinal cord. An HRP and autoradiographical tracing study in the cat.

Authors:  G Holstege; R J Cowie
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

5.  An intracellular HRP-study of cat tensor tympani motoneurons.

Authors:  E Friauf; R Baker
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

6.  A morphometric study of the soma, first-order dendrites and proximal axon of cat lumbar alpha-motoneurones intracellularly labelled with HRP.

Authors:  B Ulfhake
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

7.  Distribution patterns of dendrites in motor neuron pools of lumbosacral spinal cord of the chicken.

Authors:  N Okado; S Homma; R Ishihara; K Kohno
Journal:  Anat Embryol (Berl)       Date:  1990

8.  Electromyographic studies of neck muscles in the intact cat. I. Patterns of recruitment underlying posture and movement during natural behaviors.

Authors:  F J Richmond; D B Thomson; G E Loeb
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

9.  Tracing of frog sensory-motor synapses by intracellular injection of horseradish peroxidase.

Authors:  R Grantyn; A I Shapovalov; B I Shiriaev
Journal:  J Physiol       Date:  1984-04       Impact factor: 5.182

10.  The Subprimary Range of Firing Is Present in Both Cat and Mouse Spinal Motoneurons and Its Relationship to Force Development Is Similar for the Two Species.

Authors:  Dennis Bo Jensen; Katinka Stecina; Jacob Wienecke; Anne Hedegaard; Natalya Sukiasyan; Hans R Hultborn; Claire Francesca Meehan
Journal:  J Neurosci       Date:  2018-09-24       Impact factor: 6.167

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