J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 405 pp 677-697
Copyright © 1988 by The Physiological Society
This Article
Right arrow Full Text (PDF)
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 Quayle, J M
Right arrow Articles by Stanfield, P R
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Quayle, J M
Right arrow Articles by Stanfield, P R

The voltage-dependent block of ATP-sensitive potassium channels of frog skeletal muscle by caesium and barium ions.

J M Quayle, N B Standen and P R Stanfield

Department of Physiology, University of Leicester.

1. Patch clamp techniques were used to study the action of external Cs+ and Ba2+ on adenosine 5'-triphosphate (ATP)-dependent K+ channels in sarcolemmal vesicles from frog skeletal muscle. Both ions block channels in a voltage-dependent fashion, block increasing with hyperpolarization. 2. The Cs+ block is flickery, mean unitary current being reduced and open-level noise increased. The concentration dependence is consistent with 1:1 binding, with a dissociation constant (Kd) of 4.1 mM at -62 mV. The Kd increases e-fold for a 20 mV depolarization. 3. The kinetics of Cs+ block were analysed by amplitude distribution analysis, and by measurement of the excess open-level variance. Both methods gave similar rate constants for blocking and unblocking; about 20 mM-1 ms-1 and 75 ms-1 at -62 mV. 4. All the voltage dependence of the Cs+ block appears to lie in the blocking reaction; unblocking is independent of voltage. 5. Ba2+ blocks with slower kinetics, so that blocking events can be resolved in single-channel records. Ba2+ reduces mean open time and causes long closings. 6. The blocking rate constant for Ba2+ was measured from the open times. It was about 1.7 mM-1 ms-1 at -62 mV and increased e-fold for a 40 mV hyperpolarization. The unblocking rate, measured from closed times, yielded a Kd of about 0.1 mM at -62 mV, in agreement with that measured from the reduction in open-state probability. 7. Our results suggest that Cs+ and Ba2+ block at sites within the channel, and provide evidence that the channel is a multi-ion pore.




This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
G. W. deHart, T. Jin, D. E. McCloskey, A. E. Pegg, and D. Sheppard
The {alpha}9{beta}1 integrin enhances cell migration by polyamine-mediated modulation of an inward-rectifier potassium channel
PNAS, May 20, 2008; 105(20): 7188 - 7193.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
P. Tammaro and F. M. Ashcroft
A mutation in the ATP-binding site of the Kir6.2 subunit of the KATP channel alters coupling with the SUR2A subunit
J. Physiol., November 1, 2007; 584(3): 743 - 753.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
M. Dawes, C. Sieniawska, T. Delves, R. Dwivedi, P. J. Chowienczyk, and J. M. Ritter
Barium Reduces Resting Blood Flow and Inhibits Potassium-Induced Vasodilation in the Human Forearm
Circulation, March 19, 2002; 105(11): 1323 - 1328.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
N. Gondo, K. Kumagai, H. Nakashima, and K. Saku
Angiotensin II provokes cesium-induced ventricular tachyarrhythmias
Cardiovasc Res, February 1, 2001; 49(2): 381 - 390.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
G. A. Figtree, C. M. Webb, and P. Collins
Tamoxifen Acutely Relaxes Coronary Arteries by an Endothelium-, Nitric Oxide-, and Estrogen Receptor-Dependent Mechanism
J. Pharmacol. Exp. Ther., November 1, 2000; 295(2): 519 - 523.
[Abstract] [Full Text]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
J. Ji, A. M. F. Salapatek, and N. E. Diamant
Inwardly rectifying K+ channels in esophageal smooth muscle
Am J Physiol Gastrointest Liver Physiol, November 1, 2000; 279(5): G951 - G960.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
G. A. Figtree, H. Griffiths, Y.-Q. Lu, C. M. Webb, K. MacLeod, and P. Collins
Plant-derived estrogens relax coronary arteries in vitro by a calcium antagonistic mechanism
J. Am. Coll. Cardiol., June 1, 2000; 35(7): 1977 - 1985.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
G. A. Figtree, Y.-q. Lu, C. M. Webb, and P. Collins
Raloxifene Acutely Relaxes Rabbit Coronary Arteries In Vitro by an Estrogen Receptor–Dependent and Nitric Oxide–Dependent Mechanism
Circulation, September 7, 1999; 100(10): 1095 - 1101.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Lara, J. J. Acevedo, and C. G. Onetti
Large-Conductance Ca2+-Activated Potassium Channels in Secretory Neurons
J Neurophysiol, September 1, 1999; 82(3): 1317 - 1325.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. Jiang and G. G. Haddad
Modulation of K+ Channels by Intracellular ATP in Human Neocortical Neurons
J Neurophysiol, January 1, 1997; 77(1): 93 - 102.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
H. Ishizaka and L. Kuo
Acidosis-Induced Coronary Arteriolar Dilation Is Mediated by ATP-Sensitive Potassium Channels in Vascular Smooth Muscle
Circ. Res., January 1, 1996; 78(1): 50 - 57.
[Abstract] [Full Text]


Home page
CirculationHome page
P. Yue, K. Chatterjee, C. Beale, P. A. Poole-Wilson, and P. Collins
Testosterone Relaxes Rabbit Coronary Arteries and Aorta
Circulation, February 15, 1995; 91(4): 1154 - 1160.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 The Physiological Society.