Microcomputer analysis and display of canine small intestinal electrical activity

1987 ◽  
Vol 25 (6) ◽  
pp. 672-676 ◽  
Author(s):  
T. G. Barnett ◽  
T. H. Koeze ◽  
M. A. Pilot ◽  
X. Y. Qin
1975 ◽  
Vol 229 (5) ◽  
pp. 1268-1276 ◽  
Author(s):  
TY El-Sharkawy ◽  
EE Daniel

Some important features of the intracellularly recorded electrical control activity of rabbit jejunal smooth muscle and its temperature dependence are reported in this study. This activity consisted of repetitive 18-mV depolarizations (control potentials (CP) or slow waves), which at 37degreesC lasted 2 s and had a frequency of 18/min and arose from a membrane potential of --55 mV. In some cells periods between CP's exhibited "diastolic" progressive depolarizations (intercontrol-potential depolarization), which may be the trigger of the CP in driving cells. While CP was usually monophasic, some cells persistently exhibited a notch early in the plateau phase. We suggest that CP consists of two components, an "initial depolarization" and a "secondary depolarization," which are usually fused together to give a monophasic potential. Cooling reduced CP frequency and prolonged its duration and caused more cells to show notching. While amplitude and rate of CP initial depolarization had low Q10's, duration and rates of onset and offset of the secondary depolarization had higher Q10's. Thus, the process responsible for secondary depolarization is more sensitive to temperature thant that underlying initial depolarization of the CP.


1982 ◽  
Vol 242 (1) ◽  
pp. C36-C40 ◽  
Author(s):  
A. W. Mangel ◽  
D. O. Nelson ◽  
J. L. Rabovsky ◽  
C. L. Prosser ◽  
J. A. Connor

In calcium-free solution, strips of cat intestinal muscle developed slow, rhythmic electrical potential changes that triggered contractions. Some strips failed to develop spontaneous electrical activity in calcium-free solution but responded with contractions to depolarization by direct electrical stimulation or by treatment with barium chloride, potassium chloride, or acetylcholine. Similar results were obtained with segments of cat stomach, colon, esophagus, bladder, uterus, and vena cava, as well as with rabbit vena cava. In calcium-free saline, rat small intestinal muscle showed fast electrical activity with accompanying development of a tetanuslike contraction. After 60 min in calcium-free solution, cat small intestinal muscle retained 17.7% of its original concentration of calcium. It is concluded that in some smooth muscles, depolarization-triggered release of intracellular calcium does not require an associated influx of calcium.


1958 ◽  
Vol 195 (2) ◽  
pp. 505-515 ◽  
Author(s):  
Duncan A. Holaday ◽  
Herbert Volk ◽  
Julian Mandell

Unipolar recordings of small intestinal potentials were obtained from chronic dog preparations with exteriorized segments of bowel, from anesthetized dogs, cats and rabbits at laparotomy and from unanesthetized human subjects. Two dominant types of electrical activity were observed and correlated with function. The first type consisted of brief, nonpropagated, spike-like negative potentials which occurred only immediately preceding and during contraction and varied in frequency of occurrence proportionate to intensity of contraction. It is concluded that they represent the action potentials of contracting muscle fibers. The second type of electrical activity consisted of a recurring complex of slow potential changes, the configuration of which varied with the region of intestine and type of preparation. The complex was most stable and most clearly defined in transplanted segments of dog jejunum. The form of the complex was not altered by anesthetics or by sympathomimetic or parasympathomimetic drugs, and was the same during inactivity as during contractions. Initiation of contractions occurred only during the relatively positive phase of the slow complex. It is concluded that the slow complex is a cyclic alteration of the resting potential of the smooth muscle cells of the intestine which originates more or less synchronously in adjacent cells and is associated with a mechanism which renders the muscle alternately relatively excitable and absolutely refractory.


1978 ◽  
Vol 23 (s1) ◽  
pp. 50-51
Author(s):  
A. Pousse ◽  
C. Mendel ◽  
J. F. Grenier

2004 ◽  
Vol 22 (1) ◽  
Author(s):  
JK Lapido ◽  
LA Bradshaw ◽  
S Halter ◽  
WO Richards

1969 ◽  
Vol 45 (528) ◽  
pp. 655-658
Author(s):  
E. Q. Archampong ◽  
S. Reinis

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