AJP - GI Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 256: G265-G274, 1989;
0193-1857/89 $5.00
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 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 Publicover, N. G.
Right arrow Articles by Sanders, K. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Publicover, N. G.
Right arrow Articles by Sanders, K. M.

AJP - Gastrointestinal and Liver Physiology, Vol 256, Issue 2 265-G274, Copyright © 1989 by American Physiological Society


ARTICLES

Are relaxation oscillators an appropriate model of gastrointestinal electrical activity?

N. G. Publicover and K. M. Sanders
Department of Physiology, University of Nevada School of Medicine, Reno 89557.

Mathematical models based on relaxation oscillators have heavily influenced the terminology and experimental designs of investigations in gastrointestinal motility for nearly two decades. Relaxation oscillator equations have been used to stimulate the electrical activities of the esophagus, stomach, small intestine, colon, and rectosigmoid region. It has been suggested that many attributes of gastrointestinal electrical activity cannot be adequately explained by classic "core-conductor" or "cable" models of excitation and conduction. This article critically reviews the relaxation oscillator model and provides an explanation for each of the putative inadequacies of core-conductor theory. Furthermore, we question whether relaxation oscillator equations are able to simulate the waveforms of gastrointestinal slow waves, alterations in waveform in response to drugs or electrical stimulation, patterns of slow-wave activity when stimulated at physiological frequencies, prolonged periods of constant resting membrane potential between gastric slow waves and electrotonic spread into inactive regions. We conclude that the relaxation oscillator equations do not fully describe gastrointestinal electrical activity; excitation and propagation can be modeled by a theory that provides for morphological features, ionic conductances, and other elements included in the cable equations.


This article has been cited by other articles:


Home page
J. Physiol.Home page
S. Nakayama, K. Shimono, H.-N. Liu, H. Jiko, N. Katayama, T. Tomita, and K. Goto
Pacemaker phase shift in the absence of neural activity in guinea-pig stomach: a microelectrode array study
J. Physiol., November 1, 2006; 576(3): 727 - 738.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
K. J. Park, G. W. Hennig, H.-T. Lee, N. J. Spencer, S. M. Ward, T. K. Smith, and K. M. Sanders
Spatial and temporal mapping of pacemaker activity in interstitial cells of Cajal in mouse ileum in situ
Am J Physiol Cell Physiol, May 1, 2006; 290(5): C1411 - C1427.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
R. J. Stevens, J. S. Weinert, and N. G. Publicover
Visualization of origins and propagation of excitation in canine gastric smooth muscle
Am J Physiol Cell Physiol, September 1, 1999; 277(3): C448 - C460.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
H. G. Preiksaitis and N. E. Diamant
Myogenic mechanism for peristalsis in the cat esophagus
Am J Physiol Gastrointest Liver Physiol, August 1, 1999; 277(2): G306 - G313.
[Abstract] [Full Text] [PDF]




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