AJP - GI Journal of Neurophysiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 279: G951-G960, 2000;
0193-1857/00 $5.00
This Article
Right arrow Full Text
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 Web of Science
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 Web of Science (5)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ji, J.
Right arrow Articles by Diamant, N. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ji, J.
Right arrow Articles by Diamant, N. E.
Vol. 279, Issue 5, G951-G960, November 2000

Inwardly rectifying K+ channels in esophageal smooth muscle

Junzhi Ji, Anne Marie F. Salapatek, and Nicholas E. Diamant

Departments of Medicine and Physiology, University of Toronto, and Playfair Neuroscience Unit, Toronto Western Hospital, Toronto, Ontario, Canada M5T 2S8

The whole cell patch-clamp technique was used to investigate whether there were inwardly rectifying K+ (Kir) channels in the longitudinal muscle of cat esophagus. Inward currents were observable on membrane hyperpolarization negative to the K+ equilibrium potential (Ek) in freshly isolated esophageal longitudinal muscle cells. The current-voltage relationship exhibited strong inward rectification with a reversal potential (Erev) of -76.5 mV. Elevation of external K+ increased the inward current amplitude and positively shifted its Erev after the Ek, suggesting that potassium ions carry this current. External Ba2+ and Cs+ inhibited this inward current, with hyperpolarization remarkably increasing the inhibition. The IC50 for Ba2+ and Cs+ at -60 mV was 2.9 and 1.6 mM, respectively. Furthermore, external Ba2+ of 10 µM moderately depolarized the resting membrane potential of the longitudinal muscle cells by 6.3 mV while inhibiting the inward rectification. We conclude that Kir channels are present in the longitudinal muscle of cat esophagus, where they contribute to its resting membrane potential.

esophageal longitudinal muscle; patch clamp; barium; cesium


This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
C. Cao, J. H. Goo, W. Lee-Kwon, and T. L. Pallone
Vasa recta pericytes express a strong inward rectifier K+ conductance
Am J Physiol Regulatory Integrative Comp Physiol, June 1, 2006; 290(6): R1601 - R1607.
[Abstract] [Full Text] [PDF]




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