|
|
||||||||
1 Department of Organismal Biology and Anatomy, The University of Chicago, Chicago, Illinois 60637; 2 Department of Neurology, University of Freiburg, D-79106 Freiburg; and 3 Department of Pediatric Neurology, University of Göttingen, D-37073 Gottingen, Germany
Ramirez, J. M., U.J.A. Quellmalz, and B. Wilken. Developmental changes in the hypoxic response of the hypoglossus respiratory motor output in vitro. J. Neurophysiol. 78: 383-392, 1997. The transverse brain stem slice of mice containing the pre-Bötzinger complex (PBC), a region essential for respiratory rhythm generation in vitro, was used to study developmental changes of the response of the in vitro respiratory network to severe hypoxia (anoxia). This preparation generates, at different postnatal stages [postnatal day (P)0-22], spontaneous rhythmic activity in hypoglossal (XII) rootlets that are known to occur in synchrony with periodic bursts of neurons in the PBC. It is assumed that this rhythmic activity reflects respiratory rhythmic activity. At all examined stages anoxia led to a biphasic response: the frequency of rhythmic XII activity initially increased ("primary augmentation") and then decreased ("secondary depression"). In neonates (P0-7), anoxia did not significantly affect the amplitude of integrated XII bursts. Secondary depression never led to a cessation of rhythmic activity. In mice older than P7, augmentation was accompanied by a significant increase in the amplitude of XII bursts. A significant decrease of the amplitude of XII bursts occurred during secondary depression. This depression led always to cessation of rhythmic activity in XII rootlets. The anoxia-induced response of the respiratory rhythmic XII motor output is biphasic and changes during development in a similar way to the in vivo respiratory network. Whether this biphasic response is due to a biphasic response of the respiratory rhythm generator and/or to a biphasic modulation of the XII motor nucleus remains unresolved and needs further cellular analysis. We propose that the transverse slice is a useful model system for examination of the mechanisms underlying the hypoxic response.
This article has been cited by other articles:
![]() |
M. K. Jaiswal and B. U. Keller Cu/Zn Superoxide Dismutase Typical for Familial Amyotrophic Lateral Sclerosis Increases the Vulnerability of Mitochondria and Perturbs Ca2+ Homeostasis in SOD1G93A Mice Mol. Pharmacol., March 1, 2009; 75(3): 478 - 489. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. R. Lorier, A. G. Huxtable, D. M. Robinson, J. Lipski, G. D. Housley, and G. D. Funk P2Y1 Receptor Modulation of the Pre-Botzinger Complex Inspiratory Rhythm Generating Network In Vitro J. Neurosci., January 31, 2007; 27(5): 993 - 1005. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Sharifullina, K. Ostroumov, and A. Nistri Metabotropic glutamate receptor activity induces a novel oscillatory pattern in neonatal rat hypoglossal motoneurones J. Physiol., February 15, 2005; 563(1): 139 - 159. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. K. Tryba and J.-M. Ramirez Hyperthermia Modulates Respiratory Pacemaker Bursting Properties J Neurophysiol, November 1, 2004; 92(5): 2844 - 2852. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. K. Kosmidis, O. Pierrefiche, and J.-F. Vibert Respiratory-Like Rhythmic Activity Can Be Produced by an Excitatory Network of Non-Pacemaker Neuron Models J Neurophysiol, August 1, 2004; 92(2): 686 - 699. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. K. Tryba and J.-M. Ramirez Response of the Respiratory Network of Mice to Hyperthermia J Neurophysiol, June 1, 2003; 89(6): 2975 - 2983. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Blitz and J.-M. Ramirez Long-Term Modulation of Respiratory Network Activity Following Anoxia In Vitro J Neurophysiol, June 1, 2002; 87(6): 2964 - 2971. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Bissonnette Mechanisms regulating hypoxic respiratory depression during fetal and postnatal life Am J Physiol Regulatory Integrative Comp Physiol, June 1, 2000; 278(6): R1391 - R1400. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. C. Solomon, N. H. Edelman, and J. A. Neubauer Pre-Botzinger Complex Functions as a Central Hypoxia Chemosensor for Respiration In Vivo J Neurophysiol, May 1, 2000; 83(5): 2854 - 2868. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. Robinson, H. Kwok, B. M. Adams, K. C. Peebles, and G. D. Funk Development of the ventilatory response to hypoxia in Swiss CD-1 mice J Appl Physiol, May 1, 2000; 88(5): 1907 - 1914. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. C. Gibson and A. J. Berger Effect of Ethanol Upon Respiratory-Related Hypoglossal Nerve Output of Neonatal Rat Brain Stem Slices J Neurophysiol, January 1, 2000; 83(1): 333 - 342. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Telgkamp and J.-M. Ramirez Differential Responses of Respiratory Nuclei to Anoxia in Rhythmic Brain Stem Slices of Mice J Neurophysiol, November 1, 1999; 82(5): 2163 - 2170. [Abstract] [Full Text] [PDF] |
||||
![]() |
S L Mironov and D W Richter L-type Ca2+ channels in inspiratory neurones of mice and their modulation by hypoxia J. Physiol., October 1, 1998; 512(1): 75 - 87. [Abstract] [Full Text] [PDF] |
||||
![]() |
J M Ramirez, U J A Quellmalz, B Wilken, and D W Richter The hypoxic response of neurones within the in vitro mammalian respiratory network J. Physiol., March 1, 1998; 507(2): 571 - 582. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |