JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 70: 1401-1411, 1993;
0022-3077/93 $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 Nunez-Abades, P. A.
Right arrow Articles by Cameron, W. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nunez-Abades, P. A.
Right arrow Articles by Cameron, W. E.

Journal of Neurophysiology, Vol 70, Issue 4 1401-1411, Copyright © 1993 by APS


ARTICLES

In vitro electrophysiology of developing genioglossal motoneurons in the rat

P. A. Nunez-Abades, J. M. Spielmann, G. Barrionuevo and W. E. Cameron
Department of Behavioral Neuroscience, University of Pittsburgh, Pennsylvania 15260.

1. Experiments were performed to determine the change in membrane properties of genioglossal (GG) motoneurons during development. Intracellular recordings were made in 127 GG motoneurons from rats postnatal ages 1-30 days. 2. The input resistance (R(in)) and the membrane time constant (t(aum)) decreased between 5-6 and 13-15 days from 84.8 +/- 25.4 (SD) to 47.0 +/- 18.9 M omega (P < 0.01) and from 10.0 +/- 4.2 to 7.3 +/- 3.3 ms (P < 0.05), respectively. During this period, the rheobase (Irh) increased (P < 0.01) from 0.13 +/- 0.07 to 0.27 +/- 0.14 nA, and the percentage of cells exhibiting inward rectification increased from 5 to 40%. Voltage threshold (Vthr) of the action potential remained unchanged postnatally. 3. There was also a postnatal change in the shape of the action potential. Specifically, between 1-2 and 5-6 days, there was a decrease (P < 0.05) in the spike half-width from 2.23 +/- 0.53 to 1.45 +/- 0.44 ms, resulting, in part, from a steepening (P < 0.05) of the slope of the falling phase of the action potential from 21.6 +/- 10.1 to 32.9 +/- 13.1 mV/ms. The slope of the rising phase also increased significantly (P < 0.01) between 1-2 and 13-15 days from 68.4 +/- 31.0 to 91.4 +/- 44.3 mV/ms. 4. The average duration of the medium afterhyperpolarization (mAHPdur) decreased (P < 0.05) between 1-2 (193 +/- 53 ms) and 5-6 days (159 +/- 43 ms). Whereas the mAHPdur was found to be independent of membrane potential, there was a linear relationship between the membrane potential and the amplitude of the medium AHP (mAHPamp). From this latter relationship, a reversal potential for the mAHPamp was extrapolated to be -87 mV. No evidence for the existence of a slow AHP was found in these developing motoneurons. 5. All cells analyzed (n = 74) displayed adaptation during the first three spikes. The subsequent firing pattern was classified into two groups, adapting and nonadapting. Cells at birth were all adapting, whereas all cells but two from animals 13 days and older were nonadapting. At the intermediate age (5-6 days), the minority (27%) was adapting and the majority (73%) was nonadapting. 6. The mean slope of primary range for the first interspike interval (1st ISI) was approximately 90 Hz/nA. This value was similar for both adapting and nonadapting cells and did not change postnatally.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Physiol.Home page
G. Z. Mentis, E. Diaz, L. B. Moran, and R. Navarrete
Early alterations in the electrophysiological properties of rat spinal motoneurones following neonatal axotomy
J. Physiol., August 1, 2007; 582(3): 1141 - 1161.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
F. Brocard, D. Verdier, I. Arsenault, J. P. Lund, and A. Kolta
Emergence of Intrinsic Bursting in Trigeminal Sensory Neurons Parallels the Acquisition of Mastication in Weanling Rats
J Neurophysiol, November 1, 2006; 96(5): 2410 - 2424.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Zeng, R. K. Powers, G. Newkirk, M. Yonkers, and M. D. Binder
Contribution of Persistent Sodium Currents to Spike-Frequency Adaptation in Rat Hypoglossal Motoneurons
J Neurophysiol, February 1, 2005; 93(2): 1035 - 1041.
[Abstract] [Full Text] [PDF]


Home page
Crit. Rev. Oral Biol. Med.Home page
A.J. Miller
ORAL AND PHARYNGEAL REFLEXES IN THE MAMMALIAN NERVOUS SYSTEM: THEIR DIVERSE RANGE IN COMPLEXITY AND THE PIVOTAL ROLE OF THE TONGUE
Crit. Rev. Oral. Biol. Med., September 1, 2002; 13(5): 409 - 425.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
F.-S. Lo and R. S. Erzurumlu
Neonatal Deafferentation Does Not Alter Membrane Properties of Trigeminal Nucleus Principalis Neurons
J Neurophysiol, March 1, 2001; 85(3): 1088 - 1096.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
P. A. Nunez-Abades, J. M. Pattillo, T. M. Hodgson, and W. E. Cameron
Role of Synaptic Inputs in Determining Input Resistance of Developing Brain Stem Motoneurons
J Neurophysiol, November 1, 2000; 84(5): 2317 - 2329.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
W. E. Cameron, P. A. Nunez-Abades, I. A. Kerman, and T. M. Hodgson
Role of Potassium Conductances in Determining Input Resistance of Developing Brain Stem Motoneurons
J Neurophysiol, November 1, 2000; 84(5): 2330 - 2339.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. W. Robinson and W. E. Cameron
Time-Dependent Changes in Input Resistance of Rat Hypoglossal Motoneurons Associated with Whole-Cell Recording
J Neurophysiol, May 1, 2000; 83(5): 3160 - 3164.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. M. Horn, G. H. Dillon, Y.-P. Fan, and T. G. Waldrop
Developmental Aspects and Mechanisms of Rat Caudal Hypothalamic Neuronal Responses to Hypoxia
J Neurophysiol, April 1, 1999; 81(4): 1949 - 1959.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
G. Hilaire and B. Duron
Maturation of the Mammalian Respiratory System
Physiol Rev, April 1, 1999; 79(2): 325 - 360.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Martin-Caraballo and J. J. Greer
Electrophysiological Properties of Rat Phrenic Motoneurons During Perinatal Development
J Neurophysiol, March 1, 1999; 81(3): 1365 - 1378.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B.-X. Gao and L. Ziskind-Conhaim
Development of Ionic Currents Underlying Changes in Action Potential Waveforms in Rat Spinal Motoneurons
J Neurophysiol, December 1, 1998; 80(6): 3047 - 3061.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. H. Singer, E. M. Talley, D. A. Bayliss, and A. J. Berger
Development of Glycinergic Synaptic Transmission to Rat Brain Stem Motoneurons
J Neurophysiol, November 1, 1998; 80(5): 2608 - 2620.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Sawczuk, R. K. Powers, and M. D. Binder
Contribution of Outward Currents to Spike-Frequency Adaptation in Hypoglossal Motoneurons of the Rat
J Neurophysiol, November 1, 1997; 78(5): 2246 - 2253.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
E. M. Talley, N. N. Sadr, and D. A. Bayliss
Postnatal Development of Serotonergic Innervation, 5-HT1A Receptor Expression, and 5-HT Responses in Rat Motoneurons
J. Neurosci., June 1, 1997; 17(11): 4473 - 4485.
[Abstract] [Full Text] [PDF]




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