JN Miami Valley Hospital
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 76: 1405-1412, 1996;
0022-3077/96 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Huang, W. X.
Right arrow Articles by He, Q.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Huang, W. X.
Right arrow Articles by He, Q.

Journal of Neurophysiology, Vol 76, Issue 3 1405-1412, Copyright © 1996 by APS


ARTICLES

High-frequency oscillations in membrane potentials of medullary inspiratory and expiratory neurons (including laryngeal motoneurons)

W. X. Huang, M. I. Cohen, Q. Yu, W. R. See and Q. He
Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

1. In midcollicular decerebrate, unanesthetized, paralyzed cats ventilated with a cycle-triggered pump system, the properties of high-frequency oscillations (HFOs, 50-100 Hz) in membrane potentials (MPs) of medullary inspiratory (I) and expiratory (E) cells were studied. Simultaneous recordings were taken from bilateral phrenic and recurrent laryngeal (RL) nerves and from cells in the intermediate ventral respiratory group (intVRG, 0-1 mm rostral to the obex) or the caudal ventral respiratory group (cVRG, 2-4 mm caudal to the obex). 2. Spectral coherence analyses were used to detect the presence of HFOs during I in I and E cell MPs. Cross-correlation histograms (CCHs) between the cell and phrenic signals were used to ascertain cell-nerve HFO phase relations and to identify cells as RL motoneurons. Of the 103 cells that had significant HFOs (cell-phrenic coherences > or = 0.1), measurable HFO peak lags in the CCH were seen in 53 cells: 1) RL cells (9 I cells and 7 E cells); and 2) other types of cell (8 intVRG I cells, 18 intVRG E cells, and 11 cVRG E cells). These cells had high HFO correlations; the cell-phrenic coherence range was 0.35-0.94, with a mean HFO frequency of 58 Hz. 3. The cell-phrenic HFO lag (in ms) was measured in the CCH as the lag of the primary peak (peak located nearest to 0 lag). The phase lag was defined as (lag of primary peak in ms)/(HFO period in ms). The phase lags differed markedly between two subsets of cells: 1) RL I cells had HFO depolarization peaks that lagged the phrenic HFO peaks (average cell-phrenic phase lag = -0.18); and 2) the non-RL cells, regardless of location (intVRG or cVRG) and type (I or E), had HFO depolarization peaks leading (preceding) the phrenic HFO peaks (average cell-phrenic phase lag = 0.28). In addition, the cVRG E cells had significantly shorter cell-phrenic phase lags than the intVRG E cells (0.23 vs. 0.31, respectively). 4. These lags can be compared with the (I unit)-phrenic phase lags (average approximately 0.3) found in earlier extracellular studies. 1) There is a transmission delay of about one half HFO cycle from excitatory I cells to RL I cells. 2) Because a depolarization peak in the MP of an E cell corresponds to the start of a hyperpolarizing wave, the excitatory bulbospinal pathways from I cells have transmission times comparable with those of the inhibitory intramedullary pathways from I cells to E cells. 5. These results indicate that study of HFO phase relations can furnish useful information on functional connectivity of medullary respiratory neurons during the I phase.


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
S. Erimaki and C. N. Christakos
Coherent Motor Unit Rhythms in the 6-10 Hz Range During Time-Varying Voluntary Muscle Contractions: Neural Mechanism and Relation to Rhythmical Motor Control
J Neurophysiol, February 1, 2008; 99(2): 473 - 483.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. N. Christakos, N. A. Papadimitriou, and S. Erimaki
Parallel Neuronal Mechanisms Underlying Physiological Force Tremor in Steady Muscle Contractions of Humans
J Neurophysiol, January 1, 2006; 95(1): 53 - 66.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Haji, M. Okazaki, H. Yamazaki, and R. Takeda
Physiological Properties of Late Inspiratory Neurons and Their Possible Involvement in Inspiratory Off-Switching in Cats
J Neurophysiol, February 1, 2002; 87(2): 1057 - 1067.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
S. Erimaki and C. N. Christakos
Occurrence of Widespread Motor-Unit Firing Correlations in Muscle Contractions: Their Role in the Generation of Tremor and Time-Varying Voluntary Force
J Neurophysiol, November 1, 1999; 82(5): 2839 - 2846.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. N. Christakos
On the Detection and Measurement of Synchrony in Neural Populations by Coherence Analysis
J Neurophysiol, December 1, 1997; 78(6): 3453 - 3459.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online