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


     


J Neurophysiol 62: 810-820, 1989;
0022-3077/89 $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 Puil, E.
Right arrow Articles by Spigelman, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Puil, E.
Right arrow Articles by Spigelman, I.

Journal of Neurophysiology, Vol 62, Issue 3 810-820, Copyright © 1989 by APS


ARTICLES

Consequences of 4-aminopyridine applications to trigeminal root ganglion neurons

E. Puil, R. M. Miura and I. Spigelman
Department of Pharmacology and Therapeutics, Faculty of Medicine, University of British Columbia, Vancouver, Canada.

1. The effects of 4-aminopyridine (4-AP) on the electrical properties of 30 trigeminal root ganglion (TRG) neurons were determined from the membrane voltage responses to step and sinusoidal current injections using intracellular microelectrode techniques in in vitro slice preparations (guinea pigs). 2. Comparisons of results from 4-AP applications (0.05-5 mM) with those from tetraethylammonium (TEA) applications (0.1-10 mM) revealed very different actions of these agents. Both agents produced an increase in input resistance and a decrease in threshold for spike generation. Applications of 4-AP increased subthreshold oscillations of the membrane potential and enhanced the repetitive spike firing evoked by intracellular injections of current pulses. However, TEA applications blocked the potential oscillations and did not exaggerate repetitive spike discharges. Spontaneous spike activity or bursts were observed in four neurons that received 4-AP applications. 3. Membrane properties were determined in 20 of the 30 neurons by fitting impedance data in the frequency domain with a four-parameter membrane model by the use of computer-intensive techniques. In the majority of neurons, the time-invariant and time-dependent membrane conductances decreased during 4-AP application. The time constant for the time-dependent conductance also decreased, suggesting that the closing of K+-channels was facilitated in the membrane. 4. Applications of 4-AP in a dose range of 50 microM-5 mM produced rapid (approximately tens of seconds) responses of the neurons, resulting in a dose-dependent increase of the impedance magnitude functions and in a leftward shift of the resonant "humps" to lower frequencies. This shift indicates that the TRG neuronal membrane is capable of producing large voltage responses to current inputs at low frequencies. Recovery from the effects of 4-AP was slow (usually greater than 30 min). 5. Applications of 4-AP at high doses (greater than or equal to 1 mM) and at various imposed membrane potentials in four neurons resulted in poorly reversible unspecific changes in certain membrane parameters (increased input capacitance and conductance) and an insensitivity of the input conductance to the imposed membrane potential. These effects could be interpreted as membrane breakdown. 6. The tendencies of TRG neurons to fire repetitively and in bursts of spikes during 4-AP application result from the increased oscillatory behavior of their membrane potentials and changes in membrane resonance induced by presumed blockade of K+ channels.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
S. Yoshida and S. Matsumoto
Effects of {alpha}-Dendrotoxin on K+ Currents and Action Potentials in Tetrodotoxin-Resistant Adult Rat Trigeminal Ganglion Neurons
J. Pharmacol. Exp. Ther., July 1, 2005; 314(1): 437 - 445.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. Amir, J. D. Kocsis, and M. Devor
Multiple Interacting Sites of Ectopic Spike Electrogenesis in Primary Sensory Neurons
J. Neurosci., March 9, 2005; 25(10): 2576 - 2585.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. Cabanes, F. Viana, and C. Belmonte
Differential Thermosensitivity of Sensory Neurons in the Guinea Pig Trigeminal Ganglion
J Neurophysiol, October 1, 2003; 90(4): 2219 - 2231.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
R. Amir, C.-N. Liu, J. D. Kocsis, and M. Devor
Oscillatory mechanism in primary sensory neurones
Brain, February 1, 2002; 125(2): 421 - 435.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. Amir, M. Michaelis, and M. Devor
Burst Discharge in Primary Sensory Neurons: Triggered by Subthreshold Oscillations, Maintained by Depolarizing Afterpotentials
J. Neurosci., February 1, 2002; 22(3): 1187 - 1198.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. Wu, C.-F. Hsiao, and S. H. Chandler
Membrane Resonance and Subthreshold Membrane Oscillations in Mesencephalic V Neurons: Participants in Burst Generation
J. Neurosci., June 1, 2001; 21(11): 3729 - 3739.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. Amir, M. Michaelis, and M. Devor
Membrane Potential Oscillations in Dorsal Root Ganglion Neurons: Role in Normal Electrogenesis and Neuropathic Pain
J. Neurosci., October 1, 1999; 19(19): 8589 - 8596.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. M. Pedroarena, I. E. Pose, J. Yamuy, M. H. Chase, and F. R. Morales
Oscillatory Membrane Potential Activity in the Soma of a Primary Afferent Neuron
J Neurophysiol, September 1, 1999; 82(3): 1465 - 1476.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. A. D. Negro and S. H. Chandler
Physiological and Theoretical Analysis of K+ Currents Controlling Discharge in Neonatal Rat Mesencephalic Trigeminal Neurons
J Neurophysiol, February 1, 1997; 77(2): 537 - 553.
[Abstract] [Full Text] [PDF]




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