help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Biophysical Journal 53: 919-934 (1988)
© 1988 the Biophysical Society

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
Services
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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Farley, J
Right arrow Articles by Rudy, B
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Farley, J
Right arrow Articles by Rudy, B

Multiple types of voltage-dependent Ca2+-activated K+ channels of large conductance in rat brain synaptosomal membranes.

J Farley and B Rudy

Department of Psychology, Princeton University, New Jersey 08544.

ABSTRACT

K+-selective ion channels from a mammalian brain synaptosomal membrane preparation were inserted into planar phospholipid bilayers on the tips of patch-clamp pipettes, and single-channel currents were measured. Multiple distinct classes of K+ channels were observed. We have characterized and described the properties of several types of voltage-dependent, Ca2+-activated K+ channels of large single-channel conductance (greater than 50 pS in symmetrical KCl solutions). One class of channels (Type I) has a 200-250-pS single-channel conductance. It is activated by internal calcium concentrations greater than 10(-7) M, and its probability of opening is increased by membrane depolarization. This channel is blocked by 1-3 mM internal concentrations of tetraethylammonium (TEA). These channels are similar to the BK channel described in a variety of tissues. A second novel group of voltage-dependent, Ca2+-activated K+ channels was also studied. These channels were more sensitive to internal calcium, but less sensitive to voltage than the large (Type I) channel. These channels were minimally affected by internal TEA concentrations of 10 mM, but were blocked by a 50 mM concentration. In this class of channels we found a wide range of relatively large unitary channel conductances (65-140 pS). Within this group we have characterized two types (75-80 pS and 120-125 pS) that also differ in gating kinetics. The various types of voltage-dependent, Ca2+-activated K+ channels described here were blocked by charybdotoxin added to the external side of the channel. The activity of these channels was increased by exposure to nanomolar concentrations of the catalytic subunit of cAMP-dependent protein kinase. These results indicate that voltage-dependent, charybdotoxin-sensitive Ca2+-activated K+ channels comprise a class of related, but distinguishable channel types. Although the Ca2+-activated (Type I and II) K+ channels can be distinguished by their single-channel properties, both could contribute to the voltage-dependent Ca2+-activated macroscopic K+ current (IC) that has been observed in several neuronal somata preparations, as well as in other cells. Some of the properties reported here may serve to distinguish which type contributes in each case. A third class of smaller (40-50 pS) channels was also studied. These channels were independent of calcium over the concentration range examined (10(-7)-10(-3) M), and were also independent of voltage over the range of pipette potentials of -60 to +60 mV.(ABSTRACT TRUNCATED AT 400 WORDS)




This article has been cited by other articles:


Home page
J. Physiol.Home page
D. Kang, C. Choe, E. Cavanaugh, and D. Kim
Properties of single two-pore domain TREK-2 channels expressed in mammalian cells
J. Physiol., August 15, 2007; 583(1): 57 - 69.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
D. Gebremedhin, K. Yamaura, C. Zhang, J. Bylund, R. C. Koehler, and D. R. Harder
Metabotropic Glutamate Receptor Activation Enhances the Activities of Two Types of Ca2+-Activated K+ Channels in Rat Hippocampal Astrocytes
J. Neurosci., March 1, 2003; 23(5): 1678 - 1687.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Huang and J. Farley
PP1 Inhibitors Depolarize Hermissenda Photoreceptors and Reduce K+ Currents
J Neurophysiol, September 1, 2001; 86(3): 1297 - 1311.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
A. Meir, S. Ginsburg, A. Butkevich, S. G. Kachalsky, I. Kaiserman, R. Ahdut, S. Demirgoren, and R. Rahamimoff
Ion Channels in Presynaptic Nerve Terminals and Control of Transmitter Release
Physiol Rev, July 1, 1999; 79(3): 1019 - 1088.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
R. N. Khan, S. K. Smith, J. J. Morrison, and M. L. J. Ashford
Ca2+ dependence and pharmacology of large-conductance K+ channels in nonlabor and labor human uterine myocytes
Am J Physiol Cell Physiol, November 1, 1997; 273(5): C1721 - C1731.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
L. E. Schechter
The Potassium Channel Blockers 4-Aminopyridine and Tetraethylammonium Increase the Spontaneous Basal Release of [3H]5-Hydroxytryptamine in Rat Hippocampal Slices
J. Pharmacol. Exp. Ther., July 1, 1997; 282(1): 262 - 270.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
X.-B. Zhou, P. Ruth, J. Schlossmann, F. Hofmann, and M. Korth
Protein Phosphatase 2A Is Essential for the Activation of Ca2+-activated K+ Currents by cGMP-dependent Protein Kinase in Tracheal Smooth Muscle and Chinese Hamster Ovary Cells
J. Biol. Chem., August 16, 1996; 271(33): 19760 - 19767.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 by the Biophysical Society.