Literature DB >> 3446220

Dendritic organization of phrenic motoneurons in the adult rat.

J V Furicchia, H G Goshgarian.   

Abstract

The dendritic organization of the phrenic nucleus as a whole was studied after injections of the B-subunit of cholera toxin conjugated to horseradish peroxidase were made into the diaphragm of adult rats. Transverse, sagittal, and horizontal sections through the phrenic nucleus (C3-C5) were incubated according to a modified tetramethylbenzidine HRP technique. The conjugated form of HRP used in this study has a special affinity for the GM1 ganglioside receptors on neuronal cell surfaces. As a result, extensive labeling of the terminal dendritic fields of a large number of phrenic motoneurons occurred simultaneously. The results showed that the majority of the dendrites of phrenic motoneurons were tightly organized rostrocaudally and confined to the boundaries of the column made up of the phrenic cell bodies. In addition, analysis of transverse and horizontal sections revealed dendritic bundles radiating at right angles to the long axis of the cell column in the following directions: dorsolateral into the dorsal half of the lateral funiculus, lateral into the lateral funiculus, ventromedial into the lateral half of the anterior funiculus, ventrolateral into the ventral half of the lateral funiculus, and dorsal into the intermediate gray matter. Some dendritic bundles were measured as far as 900 microns from phrenic cell bodies into the white matter. The horizontal sections also showed that there was a periodicity in the arrangement of the dendritic fascicles in that they were separated by distances ranging from 180 to 250 microns. From the analysis of phrenic dendritic distribution the present results suggest that the majority of synaptic input to phrenic motoneurons occurs within the column of the phrenic cell bodies. In addition, there is evidence to suggest that a synaptic input may also occur directly on distal phrenic dendrites in the lateral and ventral funiculi of the spinal cord white matter.

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Year:  1987        PMID: 3446220     DOI: 10.1016/0014-4886(87)90224-x

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  23 in total

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Authors:  Kathryn M Lenz; M Dean Graham; Mayte Parada; Alison S Fleming; Dale R Sengelaub; D Ashley Monks
Journal:  Dev Neurobiol       Date:  2008-03       Impact factor: 3.964

2.  Descending input from the hypothalamic paraventricular nucleus to sympathetic preganglionic neurons in the rat.

Authors:  Y Hosoya; Y Sugiura; N Okado; A D Loewy; K Kohno
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

Review 3.  Key aspects of phrenic motoneuron and diaphragm muscle development during the perinatal period.

Authors:  Carlos B Mantilla; Gary C Sieck
Journal:  J Appl Physiol (1985)       Date:  2008-04-10

4.  The role of spinal GABAergic circuits in the control of phrenic nerve motor output.

Authors:  Vitaliy Marchenko; Michael G Z Ghali; Robert F Rogers
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2015-04-01       Impact factor: 3.619

5.  Coupling multielectrode array recordings with silver labeling of recording sites to study cervical spinal network connectivity.

Authors:  K A Streeter; M D Sunshine; S R Patel; S S Liddell; L E Denholtz; P J Reier; D D Fuller; D M Baekey
Journal:  J Neurophysiol       Date:  2016-12-14       Impact factor: 2.714

6.  Phrenic motoneuron structural plasticity across models of diaphragm muscle paralysis.

Authors:  Carlos B Mantilla; Wen-Zhi Zhan; Heather M Gransee; Y S Prakash; Gary C Sieck
Journal:  J Comp Neurol       Date:  2018-11-08       Impact factor: 3.215

7.  The phrenic motor nucleus in the adult mouse.

Authors:  K Qiu; M A Lane; K Z Lee; P J Reier; D D Fuller
Journal:  Exp Neurol       Date:  2010-09-15       Impact factor: 5.330

8.  Glutamatergic input varies with phrenic motor neuron size.

Authors:  Sabhya Rana; Carlos B Mantilla; Gary C Sieck
Journal:  J Neurophysiol       Date:  2019-08-07       Impact factor: 2.714

9.  The pattern and extent of retrograde transsynaptic transport of WGA-Alexa 488 in the phrenic motor system is dependent upon the site of application.

Authors:  Harry G Goshgarian; Janelle L Buttry
Journal:  J Neurosci Methods       Date:  2013-11-12       Impact factor: 2.390

10.  Shedding light on restoring respiratory function after spinal cord injury.

Authors:  Warren J Alilain; Jerry Silver
Journal:  Front Mol Neurosci       Date:  2009-10-30       Impact factor: 5.639

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