Literature DB >> 17913982

Spatial and functional architecture of the mammalian brain stem respiratory network: a hierarchy of three oscillatory mechanisms.

J C Smith1, A P L Abdala, H Koizumi, I A Rybak, J F R Paton.   

Abstract

Mammalian central pattern generators (CPGs) producing rhythmic movements exhibit extremely robust and flexible behavior. Network architectures that enable these features are not well understood. Here we studied organization of the brain stem respiratory CPG. By sequential rostral to caudal transections through the pontine-medullary respiratory network within an in situ perfused rat brain stem-spinal cord preparation, we showed that network dynamics reorganized and new rhythmogenic mechanisms emerged. The normal three-phase respiratory rhythm transformed to a two-phase and then to a one-phase rhythm as the network was reduced. Expression of the three-phase rhythm required the presence of the pons, generation of the two-phase rhythm depended on the integrity of Bötzinger and pre-Bötzinger complexes and interactions between them, and the one-phase rhythm was generated within the pre-Bötzinger complex. Transformation from the three-phase to a two-phase pattern also occurred in intact preparations when chloride-mediated synaptic inhibition was reduced. In contrast to the three-phase and two-phase rhythms, the one-phase rhythm was abolished by blockade of persistent sodium current (I(NaP)). A model of the respiratory network was developed to reproduce and explain these observations. The model incorporated interacting populations of respiratory neurons within spatially organized brain stem compartments. Our simulations reproduced the respiratory patterns recorded from intact and sequentially reduced preparations. Our results suggest that the three-phase and two-phase rhythms involve inhibitory network interactions, whereas the one-phase rhythm depends on I(NaP). We conclude that the respiratory network has rhythmogenic capabilities at multiple levels of network organization, allowing expression of motor patterns specific for various physiological and pathophysiological respiratory behaviors.

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Year:  2007        PMID: 17913982      PMCID: PMC2225347          DOI: 10.1152/jn.00985.2007

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  69 in total

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2.  Opioid-induced quantal slowing reveals dual networks for respiratory rhythm generation.

Authors:  Nicholas M Mellen; Wiktor A Janczewski; Christopher M Bocchiaro; Jack L Feldman
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Review 3.  Functional and structural models of pontine modulation of mechanoreceptor and chemoreceptor reflexes.

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Journal:  Respir Physiol Neurobiol       Date:  2004-11-15       Impact factor: 1.931

Review 4.  Biological pattern generation: the cellular and computational logic of networks in motion.

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Journal:  Neuron       Date:  2006-12-07       Impact factor: 17.173

5.  A decerebrate, artificially-perfused in situ preparation of rat: utility for the study of autonomic and nociceptive processing.

Authors:  Anthony E Pickering; Julian F R Paton
Journal:  J Neurosci Methods       Date:  2006-02-23       Impact factor: 2.390

6.  A model of respiratory rhythm generation.

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Journal:  Neuroreport       Date:  1991-10       Impact factor: 1.837

7.  The Kölliker-Fuse nucleus gates the postinspiratory phase of the respiratory cycle to control inspiratory off-switch and upper airway resistance in rat.

Authors:  Mathias Dutschmann; Horst Herbert
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8.  Evidence for glycinergic respiratory neurons: Bötzinger neurons express mRNA for glycinergic transporter 2.

Authors:  A M Schreihofer; R L Stornetta; P G Guyenet
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9.  Primary respiratory rhythm generator in the medulla of brainstem-spinal cord preparation from newborn rat.

Authors:  H Onimaru; A Arata; I Homma
Journal:  Brain Res       Date:  1988-04-05       Impact factor: 3.252

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  171 in total

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Journal:  J Comput Neurosci       Date:  2010-10-07       Impact factor: 1.621

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Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-04       Impact factor: 11.205

3.  Preinspiratory calcium rise in putative pre-Botzinger complex astrocytes.

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Journal:  J Neurophysiol       Date:  2010-09-08       Impact factor: 2.714

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Journal:  Brain Struct Funct       Date:  2012-01-28       Impact factor: 3.270

6.  Pre- and post-inspiratory neurons change their firing properties in female rats exposed to chronic intermittent hypoxia.

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Journal:  Neuroscience       Date:  2019-03-28       Impact factor: 3.590

7.  Eupnea, tachypnea, and autoresuscitation in a closed-loop respiratory control model.

Authors:  Casey O Diekman; Peter J Thomas; Christopher G Wilson
Journal:  J Neurophysiol       Date:  2017-07-19       Impact factor: 2.714

8.  Generation of active expiration by serotoninergic mechanisms of the ventral medulla of rats.

Authors:  Eduardo V Lemes; Eduardo Colombari; Daniel B Zoccal
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Review 9.  Brainstem respiratory networks: building blocks and microcircuits.

Authors:  Jeffrey C Smith; Ana P L Abdala; Anke Borgmann; Ilya A Rybak; Julian F R Paton
Journal:  Trends Neurosci       Date:  2012-12-17       Impact factor: 13.837

10.  Increased sympathetic outflow in juvenile rats submitted to chronic intermittent hypoxia correlates with enhanced expiratory activity.

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Journal:  J Physiol       Date:  2008-05-01       Impact factor: 5.182

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