AJP - Regu Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol (September 27, 2002). doi:10.1152/ajpregu.00303.2002
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
284/2/R558    most recent
00303.2002v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 Nielsen, J. J.
Right arrow Articles by Juel, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nielsen, J. J.
Right arrow Articles by Juel, C.

Articles in PresS, published online ahead of print September 26, 2002
Am J Physiol Regu Physiol, 10.1152/ajpregu.00303.2002
Submitted on May 28, 2002
Accepted on September 23, 2002

Localization and function of ATP-sensitive potassium channels in human skeletal muscle

Jens Jung Nielsen1, Michael Kristensen2, Ylva Hellsten1, Jens Bangsbo1, and Carsten Juel2*

1 Institute of Exercise and Sports Sciences, Copenhagen Muscle Research Centre, Copenhagen, Denmark
2 August Krogh Institute, University of Copenhagen, Copenhagen Muscle Research Centre, Copenhagen, Denmark

* To whom correspondence should be addressed. E-mail: cjuel{at}aki.ku.dk.

The present study investigated the localization of ATP sensitive K+ channels (KATP channels) in human skeletal muscle and the functional importance of these channels for human muscle K+ distribution at rest and during muscle activity. Membrane fractionation based on either the giant vesicle technique or the sucrose-gradient technique in combination with Western blotting demonstrated that the KATP channels are mainly located in the sarcolemma. This localization was confirmed by immunohistochemical measurements. With the microdialysis technique it was demonstrated that local application of the KATP channel inhibitor glibenclamide reduced (P<0.05) interstitial K+ at rest from approximately 4.5 to 4.0 mM, whereas the concentration in the control leg remained constant. Glibenclamide had no effect on the interstitial K+ accumulation during knee-extensor exercise at a power output of 60 W. In contrast to what has been found during in vitro conditions, the present study demonstrated that under in vivo conditions the KATP channels are active at rest and contribute to the accumulation of interstitial K+.




This article has been cited by other articles:


Home page
Physiol. Rev.Home page
D. G. Allen, G. D. Lamb, and H. Westerblad
Skeletal Muscle Fatigue: Cellular Mechanisms
Physiol Rev, January 1, 2008; 88(1): 287 - 332.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
D. Zheng, A. Perianayagam, D. H. Lee, M. D. Brannan, L. E. Yang, D. Tellalian, P. Chen, K. Lemieux, A. Marette, J. H. Youn, et al.
AMPK activation with AICAR provokes an acute fall in plasma [K+]
Am J Physiol Cell Physiol, January 1, 2008; 294(1): C126 - C135.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
M. Broch-Lips, K. Overgaard, H. A. Praetorius, and O. B. Nielsen
Effects of extracellular HCO3 on fatigue, pHi, and K+ efflux in rat skeletal muscles
J Appl Physiol, August 1, 2007; 103(2): 494 - 503.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. J. McKenna, I. Medved, C. A. Goodman, M. J. Brown, A. R. Bjorksten, K. T. Murphy, A. C. Petersen, S. Sostaric, and X. Gong
N-acetylcysteine attenuates the decline in muscle Na+,K+-pump activity and delays fatigue during prolonged exercise in humans
J. Physiol., October 1, 2006; 576(1): 279 - 288.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
W. G. Schrage, N. M. Dietz, and M. J. Joyner
Effects of combined inhibition of ATP-sensitive potassium channels, nitric oxide, and prostaglandins on hyperemia during moderate exercise
J Appl Physiol, May 1, 2006; 100(5): 1506 - 1512.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
M. Kristensen, T. Hansen, and C. Juel
Membrane proteins involved in potassium shifts during muscle activity and fatigue
Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2006; 290(3): R766 - R772.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
D. Street, J.-J. Nielsen, J. Bangsbo, and C. Juel
Metabolic alkalosis reduces exercise-induced acidosis and potassium accumulation in human skeletal muscle interstitium
J. Physiol., July 15, 2005; 566(2): 481 - 489.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
M. Thabet, T. Miki, S. Seino, and J.-M. Renaud
Treadmill running causes significant fiber damage in skeletal muscle of KATP channel-deficient mice
Physiol Genomics, July 14, 2005; 22(2): 204 - 212.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. K. Hansen, T. Clausen, and O. B. Nielsen
Effects of lactic acid and catecholamines on contractility in fast-twitch muscles exposed to hyperkalemia
Am J Physiol Cell Physiol, July 1, 2005; 289(1): C104 - C112.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. R. Gosmanov, Z. Fan, X. Mi, E. G. Schneider, and D. B. Thomason
ATP-sensitive potassium channels mediate hyperosmotic stimulation of NKCC in slow-twitch muscle
Am J Physiol Cell Physiol, March 1, 2004; 286(3): C586 - C595.
[Abstract] [Full Text]


Home page
J. Physiol.Home page
J. J. Nielsen, M. Mohr, C. Klarskov, M. Kristensen, P. Krustrup, C. Juel, and J. Bangsbo
Effects of high-intensity intermittent training on potassium kinetics and performance in human skeletal muscle
J. Physiol., February 1, 2004; 554(3): 857 - 870.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2002 by the American Physiological Society.