J Physiol Society Meetings
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 552, Number 2, 483-497, October 15, 2003 DOI: 10.1113/jphysiol.2003.050120
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
552/2/483    most recent
jphysiol.2003.050120v1
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 Faber, E. S. L.
Right arrow Articles by Sah, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Faber, E. S. L.
Right arrow Articles by Sah, P.
J Physiol (2003), 552.2, pp. 483-497
© Copyright 2003 D 2003 The Physiological Society
DOI: 10.1113/jphysiol.2003.050120

Ca2+-activated K+ (BK) channel inactivation contributes to spike broadening during repetitive firing in the rat lateral amygdala

E. S. Louise Faber and Pankaj Sah

Queensland Brain Institute, University of Queensland, St Lucia, Queensland and Division of Neuroscience, John Curtin School of Medical Research, Australian National University, Canberra, Australia

In many neurons, trains of action potentials show frequency-dependent broadening. This broadening results from the voltage-dependent inactivation of K+ currents that contribute to action potential repolarisation. In different neuronal cell types these K+ currents have been shown to be either slowly inactivating delayed rectifier type currents or rapidly inactivating A-type voltage-gated K+ currents. Recent findings show that inactivation of a Ca2+-dependent K+ current, mediated by large conductance BK-type channels, also contributes to spike broadening. Here, using whole-cell recordings in acute slices, we examine spike broadening in lateral amygdala projection neurons. Spike broadening is frequency dependent and is reversed by brief hyperpolarisations. This broadening is reduced by blockade of voltage-gated Ca2+ channels and BK channels. In contrast, broadening is not blocked by high concentrations of 4-aminopyridine (4-AP) or alpha-dendrotoxin. We conclude that while inactivation of BK-type Ca2+-activated K+ channels contributes to spike broadening in lateral amygdala neurons, inactivation of another as yet unidentified outward current also plays a role.



This article has been cited by other articles:


Home page
J. Neurosci.Home page
Y. Fu and V. Neugebauer
Differential Mechanisms of CRF1 and CRF2 Receptor Functions in the Amygdala in Pain-Related Synaptic Facilitation and Behavior
J. Neurosci., April 9, 2008; 28(15): 3861 - 3876.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
D. J. Loane, P. A. Lima, and N. V. Marrion
Co-assembly of N-type Ca2+ and BK channels underlies functional coupling in rat brain
J. Cell Sci., March 15, 2007; 120(6): 985 - 995.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. Likhtik, J. G. Pelletier, A. T. Popescu, and D. Pare
Identification of Basolateral Amygdala Projection Cells and Interneurons Using Extracellular Recordings
J Neurophysiol, December 1, 2006; 96(6): 3257 - 3265.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
D. Oliver, A. M. Taberner, H. Thurm, M. Sausbier, C. Arntz, P. Ruth, B. Fakler, and M. C. Liberman
The role of BKCa channels in electrical signal encoding in the mammalian auditory periphery.
J. Neurosci., June 7, 2006; 26(23): 6181 - 6189.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
T. F. Finnegan, S.-R. Chen, and H.-L. Pan
{micro} Opioid Receptor Activation Inhibits GABAergic Inputs to Basolateral Amygdala Neurons Through Kv1.1/1.2 Channels
J Neurophysiol, April 1, 2006; 95(4): 2032 - 2041.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
J. Kim, D.-S. Wei, and D. A. Hoffman
Kv4 potassium channel subunits control action potential repolarization and frequency-dependent broadening in rat hippocampal CA1 pyramidal neurones
J. Physiol., November 15, 2005; 569(1): 41 - 57.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. K. Bahia, R. Suzuki, D. C. H. Benton, A. J. Jowett, M. X. Chen, Derek. J. Trezise, A. H. Dickenson, and G. W. J. Moss
A Functional Role for Small-Conductance Calcium-Activated Potassium Channels in Sensory Pathways Including Nociceptive Processes
J. Neurosci., April 6, 2005; 25(14): 3489 - 3498.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
W. Ouyang and H. C. Hemmings Jr.
Depression by Isoflurane of the Action Potential and Underlying Voltage-Gated Ion Currents in Isolated Rat Neurohypophysial Nerve Terminals
J. Pharmacol. Exp. Ther., February 1, 2005; 312(2): 801 - 808.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
X.-P. Sun, B. Yazejian, and A. D. Grinnell
Electrophysiological properties of BK channels in Xenopus motor nerve terminals
J. Physiol., May 15, 2004; 557(1): 207 - 228.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 The Physiological Society.