 |
Previous Article | Next Article 
The Journal of Neuroscience, November 1, 2001, 21(21):8680-8689
Altered Respiratory Motor Drive after Spinal Cord Injury:
Supraspinal and Bilateral Effects of a Unilateral Lesion
Francis J.
Golder1,
Paul J.
Reier2, and
Donald
C.
Bolser1
1 Department of Physiological Sciences, College of
Veterinary Medicine, and 2 Department of Neuroscience,
University of Florida, Gainesville, Florida 32610
Because some bulbospinal respiratory premotor neurons have
bilateral projections to the phrenic nuclei, we investigated whether changes in contralateral phrenic motoneuron function would occur after
unilateral axotomy via C2 hemisection. Phrenic neurograms were recorded under baseline conditions and during hypercapnic and
hypoxic challenge in C2 hemisected, normal, and
sham-operated rats at 1 and 2 months after injury. The rats were
anesthetized, vagotomized, and mechanically ventilated. No group
differences were seen in contralateral neurograms at 1 month after
injury. At 2 months, however, there was a statistically significant
decrease in respiratory rate (RR) at normocapnia, an elevated RR during hypoxia, and an attenuated increase in phrenic neurogram amplitude during hypercapnia in the C2-hemisected animals. To test
whether C2 hemisection had induced a supraspinal change in
respiratory motor drive, we recorded ipsilateral and contralateral
hypoglossal neurograms during hypercapnia. As with the phrenic motor
function data, no change in hypoglossal output was evident until 2 months had elapsed when hypoglossal amplitudes were significantly
decreased bilaterally. Last, the influence of serotonin-containing
neurons on the injury-induced change in phrenic motoneuron function was examined in rats treated with the serotonin neurotoxin,
5,7-dihydroxytryptamine. Pretreatment with 5,7-dihydroxytryptamine
prevented the effects of C2 hemisection on contralateral
phrenic neurogram amplitude and normalized the change in RR during
hypoxia. The results of this study show novel neuroplastic changes in
segmental and brainstem respiratory motor output after C2
hemisection that coincided with the spontaneous recovery of some
ipsilateral phrenic function. Some of these effects may be modulated by
serotonin-containing neurons.
Key words:
hypercapnia; hypoglossal; hypoxia; phrenic; rats; serotonin; spinal cord injury; ventilation
Copyright © 2001 Society for Neuroscience 0270-6474/01/21218680-10$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
D. D. Fuller, F. J. Golder, E. B. Olson Jr., and G. S. Mitchell
Recovery of phrenic activity and ventilation after cervical spinal hemisection in rats
J Appl Physiol,
March 1, 2006;
100(3):
800 - 806.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. M. Johnson and R. J. Creighton
Spinal cord injury-induced changes in breathing are not due to supraspinal plasticity in turtles (Pseudemys scripta)
Am J Physiol Regulatory Integrative Comp Physiol,
December 1, 2005;
289(6):
R1550 - R1561.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. Choi, W.-L. Liao, K. M. Newton, R. C. Onario, A. M. King, F. C. Desilets, E. J. Woodard, M. E. Eichler, W. R. Frontera, S. Sabharwal, et al.
Respiratory Abnormalities Resulting from Midcervical Spinal Cord Injury and their Reversal by Serotonin 1A Agonists in Conscious Rats
J. Neurosci.,
May 4, 2005;
25(18):
4550 - 4559.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. J. Golder and G. S. Mitchell
Spinal Synaptic Enhancement with Acute Intermittent Hypoxia Improves Respiratory Function after Chronic Cervical Spinal Cord Injury
J. Neurosci.,
March 16, 2005;
25(11):
2925 - 2932.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. D. Fuller, S. M. Johnson, E. B. Olson Jr, and G. S. Mitchell
Synaptic Pathways to Phrenic Motoneurons Are Enhanced by Chronic Intermittent Hypoxia after Cervical Spinal Cord Injury
J. Neurosci.,
April 1, 2003;
23(7):
2993 - 3000.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. J. Golder, D. D. Fuller, P. W. Davenport, R. D. Johnson, P. J. Reier, and D. C. Bolser
Respiratory Motor Recovery after Unilateral Spinal Cord Injury: Eliminating Crossed Phrenic Activity Decreases Tidal Volume and Increases Contralateral Respiratory Motor Output
J. Neurosci.,
March 15, 2003;
23(6):
2494 - 2501.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. B. Mantilla and G. C. Sieck
Plasticity in Respiratory Motor Control: Invited Review: Mechanisms underlying motor unit plasticity in the respiratory system
J Appl Physiol,
March 1, 2003;
94(3):
1230 - 1241.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
K. F. Morris, D. M. Baekey, S. C. Nuding, T. E. Dick, R. Shannon, and B. G. Lindsey
Plasticity in Respiratory Motor Control: Invited Review: Neural network plasticity in respiratory control
J Appl Physiol,
March 1, 2003;
94(3):
1242 - 1252.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
H. G. Goshgarian
Plasticity in Respiratory Motor Control: Invited Review: The crossed phrenic phenomenon: a model for plasticity in the respiratory pathways following spinal cord injury
J Appl Physiol,
February 1, 2003;
94(2):
795 - 810.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. S. Mitchell and S. M. Johnson
Plasticity in Respiratory Motor Control: Invited Review: Neuroplasticity in respiratory motor control
J Appl Physiol,
January 1, 2003;
94(1):
358 - 374.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|