Literature DB >> 7798382

Brainstem network controlling descending drive to phrenic motoneurons in rat.

E G Dobbins1, J L Feldman.   

Abstract

Contraction of the diaphragm is controlled by phrenic motoneurons that receive input from sources that are not fully established. Bulbospinal (second-order) neurons projecting to phrenic motoneurons and propriobulbar (third-order) neurons projecting to these bulbspinal neurons were investigated in rat by transsynaptic transport of the neuroinvasive pseudorabies virus. Bulbospinal neurons were located predominantly in the medullary lateral tegmental field in two functionally described regions, the ventral respiratory group and Bötzinger complex. An intervening region, the pre-Bötzinger complex, contained essentially no phrenic premotoneurons. Bulbospinal neurons were also located in ventral, interstitial, and ventrolateral subnuclei of the solitary tract, and gigantocellular, Kölliker-Fuse, parabrachial, and medullary raphe nuclei. A monosynaptic pathway to phrenic motoneurons from the nucleus of the solitary tract was confirmed; monosynaptic pathways from upper cervical spinal cord, spinal trigeminal nucleus, medical and lateral vestibular nuclei, and medial pontine tegmentum were not verified. Locations of third-order neurons were consistent with described projections to the ventral respiratory group, from contralateral ventral respiratory group, Bötzinger complex, A5 noradrenergic cell group, and the following nuclei; solitary, raphe, Kölliker-Fuse, parabrachial, retrotrapezoid, and paragigantocellular. Novel findings included a projection from locus coeruleus to respiratory premotoneurons and the lack of previously described pathways from area postrema and spinal trigeminal nucleus. These second- and third-order neurons from the output network for diphragm motor control which includes numerous behaviors (e.g., respiration, phonation, defecation). Of the premotoneurons, the rostral ventral respiratory group is the primary population controlling phrenic motoneurons.

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Mesh:

Year:  1994        PMID: 7798382     DOI: 10.1002/cne.903470106

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


  143 in total

1.  Transient, reversible apnoea following ablation of the pre-Bötzinger complex in rats.

Authors:  R St-Jacques; W M St-John
Journal:  J Physiol       Date:  1999-10-01       Impact factor: 5.182

2.  The pre-Bötzinger complex participates in generating the respiratory effects of thyroliberin.

Authors:  A N Inyushkin; N A Merkulova; S A Chepurnov
Journal:  Neurosci Behav Physiol       Date:  1999 May-Jun

Review 3.  Recent insights into hyperventilation from the study of Rett syndrome.

Authors:  A M Kerr; P O Julu
Journal:  Arch Dis Child       Date:  1999-04       Impact factor: 3.791

4.  Concurrent inhibition and excitation of phrenic motoneurons during inspiration: phase-specific control of excitability.

Authors:  M A Parkis; X Dong; J L Feldman; G D Funk
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

5.  Endogenous excitatory drive to the respiratory system in rapid eye movement sleep in cats.

Authors:  J Orem; A T Lovering; W Dunin-Barkowski; E H Vidruk
Journal:  J Physiol       Date:  2000-09-01       Impact factor: 5.182

Review 6.  Breathing: rhythmicity, plasticity, chemosensitivity.

Authors:  Jack L Feldman; Gordon S Mitchell; Eugene E Nattie
Journal:  Annu Rev Neurosci       Date:  2003-02-13       Impact factor: 12.449

7.  Synaptic pathways to phrenic motoneurons are enhanced by chronic intermittent hypoxia after cervical spinal cord injury.

Authors:  David D Fuller; Stephen M Johnson; E Burdette Olson; Gordon S Mitchell
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

8.  Projections of preBötzinger complex neurons in adult rats.

Authors:  Wenbin Tan; Silvia Pagliardini; Paul Yang; Wiktor A Janczewski; Jack L Feldman
Journal:  J Comp Neurol       Date:  2010-05-15       Impact factor: 3.215

9.  Defining ventral medullary respiratory compartments with a glutamate receptor agonist in the rat.

Authors:  A Monnier; G F Alheid; D R McCrimmon
Journal:  J Physiol       Date:  2003-03-14       Impact factor: 5.182

10.  Serotonergic projections from the caudal raphe nuclei to the hypoglossal nucleus in male and female rats.

Authors:  Jessica R Barker; Cathy F Thomas; Mary Behan
Journal:  Respir Physiol Neurobiol       Date:  2008-11-27       Impact factor: 1.931

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