Electrical transmission of slow waves from longitudinal to circular intestinal muscle

1965 ◽  
Vol 209 (6) ◽  
pp. 1254-1260 ◽  
Author(s):  
Alex Bortoff
Keyword(s):  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Complete Removal ◽  
Intestinal Wall ◽  
Slow Waves ◽  
Electrical Transmission ◽  
Circular Layer ◽  
Spontaneous Rhythmicity ◽  
Longitudinal Layer ◽  
Rhythmical Contractions

Circular muscle from cat intestine exhibits spontaneous rhythmical contractions only when it is attached to longitudinal muscle. Under these conditions electrical slow waves can be recorded from circular muscle, but they disappear following complete removal of the longitudinal layer. If a small patch of longitudinal muscle remains, slow waves can be recorded from adjacent circular muscle. Those recorded lateral to the longitudinal layer are synchronized with slow waves recorded directly from this layer. Their amplitude decreases exponentially with distance, approaching zero at about 12 mm from the lateral edges and about 3 mm from the oral or aboral edge of the longitudinal layer. Slow waves can also be recorded across the entire intestinal wall or across a longitudinal-circular muscle preparation. With this method of recording, the amplitude of the slow waves decreases as the thickness of the circular layer is reduced by stripping away its innermost layers. The amplitude is not increased by replacing these layers. These results indicate that slow waves may be transmitted electrotonically from longitudinal to circular muscle, implying the existence of electrical continuity between the two muscle layers. The transmission of slow waves can account for the coordinated spontaneous rhythmicity exhibited by circular muscle under normal conditions, i.e., when attached to the longitudinal layer.

Electrical and mechanical interactions between the muscle layers of canine proximal colon

1990 ◽  
Vol 258 (3) ◽  
pp. G484-G491 ◽  
Author(s):  
P. J. Sabourin ◽  
Y. J. Kingma ◽  
K. L. Bowes
Keyword(s):  
Membrane Potential ◽  
Circular Muscle ◽  
Longitudinal Direction ◽  
Proximal Colon ◽  
Slow Waves ◽  
The Other ◽  
Potential Oscillations ◽  
Circular Layer ◽  
Longitudinal Layer ◽  
Membrane Potential Oscillations

Electrical and mechanical interactions between the two smooth muscle layers of canine colon have been studied using a dual sucrose gap apparatus. Muscle samples were dissected into an L-shape, with one leg cut in the circular direction and the other cut in the longitudinal direction. Longitudinal muscle was removed from the circular leg and circular muscle was removed from the longitudinal leg. The bend of the L contained both layers. The activity of the two layers was studied simultaneously under basal conditions, after stimulation by neostigmine and carbachol, and in the presence of tetrodotoxin. Interactions were more common after stimulation and were marked by modification of one layer's mechanical and electrical activity during increased activity in the other layer. Two patterns were commonly observed. First, during a burst of membrane potential oscillations and spike potentials in the longitudinal layer, slow waves in the circular layer developed spike potentials and some slow waves were also prolonged. Second, during a slow-wave cycle in the circular layer, the amplitude of membrane potential oscillations in the longitudinal layer was increased with an associated increase in the incidence of spike potentials. These interactions were associated with contractions of increased strength, which were similar in both layers. All interactions continued after nerve-conduction blockade by tetrodotoxin.

Origin and propagation of electrical slow waves in circular muscle of canine proximal colon

1987 ◽  
Vol 252 (2) ◽  
pp. C215-C224 ◽  
Author(s):  
T. K. Smith ◽  
J. B. Reed ◽  
K. M. Sanders
Keyword(s):  
Slow Wave ◽  
Circular Muscle ◽  
Proximal Colon ◽  
Slow Waves ◽  
Thin Strip ◽  
Colon Cells ◽  
Cable Properties ◽  
Wave Event ◽  
Circular Layer ◽  
Longitudinal Layer

Experiments to determine the site of slow-wave origin and the mechanism of propagation were performed on muscles of the canine proximal colon. Cells along the submucosal border of the circular layer had resting membrane potentials (RMP) averaging -78 mV, and slow waves, 40 mV in amplitude. The RMP of cells through the thickness of the circular layer decreased exponentially with distance from the submucosal border, such that RMPs of circular cells at the myenteric border were only -43 mV. Slow waves decreased in amplitude through the thickness such that slow waves could not be detected adjacent to the myenteric border. When a thin strip of muscle along the submucosal border was removed, slow waves were not recorded from the bulk of the circular layer and could not be evoked by acetylcholine. Slow waves were still present in the excised strip. Experiments to determine the rate of slow-wave propagation were also performed. Two cells were impaled, one at the submucosal surface, and another at some distance through the circular layer. Slow waves occurred nearly simultaneously at both sites. What latency was observed could be explained on the basis of electrotonic conduction. The results support the hypothesis that in the canine proximal colon slow waves are generated at the extreme submucosal surface of the circular layer. The bulk of the circular layer does not possess either pacemaker or regenerative mechanisms, and slow waves propagate passively toward the myenteric border. The cable properties of the circular muscle syncytium furnish a barrier to invasion of the longitudinal layer by the slow wave event.

The Morphology of the Gut of the Brown Trout (Salmo trutta)

1959 ◽  
Vol s3-100 (50) ◽  
pp. 183-198
Author(s):  
G. BURNSTOCK
Keyword(s):  
Smooth Muscle ◽  
Salmo Trutta ◽  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Living System ◽  
Cardiac Stomach ◽  
Longitudinal Smooth Muscle ◽  
Brown Trout Salmo Trutta ◽  
Pyloric Stomach ◽  
Longitudinal Layer

1. In the trout gut a short oesophagus containing only striated circular muscles opens into a large cardiac stomach possessing inner circular and outer longitudinal smooth muscle-coats, as well as a musculsris mucosse. Ahout 45 pyloric caeca come off the intestine, which, while containing muscle-coats, does not possess a muscularis mucosae. In the rectum, the longitudinal muscle is as thick as the circular muscle-coat, hut in other regions the circular muscle is dominant, especially in the pyloric stomach where it is over 10 times as thick ss the longitudinal layer. 2. The mucosa is distinguished by the presence of a prominent layer of dense collagen, the stratum compactum, which is perforated only by nerves and blood-vessels. This layer forms a firm and relatively inextensible (approximately 10% extensibility) basis to the gut-wall. It limits the extensibility of the smooth muscle to 75% radially in the stomach and 25% radially and longitudinally in the intestine. In contrast, the stomachs of the pike and perch, which do not possess a stratum compactum, extend up so 200%. 3. A detailed description of the regional junctions and sphincters gives a basis for the interpretation of events occurring in the living system. Valves at the junction of the pneumatic duct with the oesophagus, and between the duodenum and pyloric stomach, serve to prevent the regurgitation of gas and semi-digested food respectively. A complex sphincter mechanism exists at the pylorus, and to a lesser extent at the antrum. A series of about five circular muscle-constrictors represents the anus. 4. It is suggested that the cells forming the stratum granulosum, a layer closely associated with the stratum compactum, are composed of active fibroblast cells producing collagen. 5. The rectum contains a muscular annulo-spiral septum of unknown function which protrudes into the lumen.

scholarly journals The three muscle layers in the pyloric sphincter and their possible function during antropyloroduodenal motility

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mi-Sun Hur ◽  
Seunggyu Lee ◽  
Tong Mook Kang ◽  
Chang-Seok Oh
Keyword(s):  
Outer Layer ◽  
Longitudinal Muscle ◽  
Middle Layer ◽  
Comprehensive Approach ◽  
Pyloric Sphincter ◽  
Muscular Tissue ◽  
Micro Ct ◽  
Circular Layer ◽  
Korean Adult ◽  
Longitudinal Layer

AbstractThis study was conducted to determine the muscular arrangement of the human pyloric sphincter using a comprehensive approach that involved microdissection, histology, and microcomputed tomography (micro‐CT). The stomachs of 80 embalmed Korean adult cadavers were obtained. In all specimens, loose muscular tissue of the innermost aspect of the sphincter wall ran aborally, forming the newly found inner longitudinal muscle bundles, entered the duodenum, and connected with the nearby circular bundles. In all specimens, approximately one-third of the outer longitudinal layer of the sphincter entered its inner circular layer, divided the circular layer into several parts, and finally connected with the circular bundles. Anatomical findings around the sphincter were confirmed in micro-CT images. The sphincter wall comprised three layers: an inner layer of longitudinal bundles, a middle layer of major circular and minor longitudinal bundles, and an outer layer of longitudinal bundles. The stomach outer longitudinal bundles were connected to the sphincter circular bundles. The inner longitudinal bundles of the sphincter were connected to the adjacent circular bundles of the duodenum.

Pacemaker activity in septal structures of canine colonic circular muscle

1990 ◽  
Vol 259 (2) ◽  
pp. G264-G273 ◽  
Author(s):  
S. M. Ward ◽  
K. M. Sanders
Keyword(s):  
Slow Wave ◽  
Electrical Coupling ◽  
Circular Muscle ◽  
Proximal Colon ◽  
Slow Waves ◽  
Pacemaker Activity ◽  
Electrical Measurements ◽  
Morphological Studies ◽  
Circular Layer ◽  
And Function

Morphological and electrophysiological experiments were performed to characterize the pacemaker areas of the circular muscle in the canine proximal colon. Morphological studies showed interstitial cells of Cajal lining the submucosal surface of the circular layer and the septal structures that separate the circular layer into bundles. Electrical measurements suggested that slow waves may propagate into the thickness of the circular muscle in a regenerative manner along the surface of these septa. Removal of the submucosal pacemaker region blocked generation of slow waves in nonseptal regions of the circular muscle, but slow-wave activity continued in the circular muscle near septa. These data suggest that slow-wave pacemaker activity is not limited to a two-dimensional surface at the submucosal surface but extends into the interior of the circular layer along septal invaginations. Experiments were also performed to determine the dominance of pacemaker activity (i.e., septal vs. submucosal), and examples were found in which both areas appeared to initiate slow waves in intact muscles. Other studies showed that slow waves could propagate across septa, suggesting some form of electrical coupling between circular muscle bundles. This study provides a more complete view of the structure and function of pacemaker areas in the canine proximal colon.

Cholinergic nerve-mediated excitation in the guinea pig choledochoduodenal junction activated by distension

1994 ◽  
Vol 267 (5) ◽  
pp. G938-G946 ◽  
Author(s):  
F. Vogalis ◽  
R. R. Bywater ◽  
G. S. Taylor
Keyword(s):  
Smooth Muscle ◽  
Guinea Pig ◽  
Action Potential ◽  
Action Potentials ◽  
Discharge Rate ◽  
Circular Muscle ◽  
Muscle Layer ◽  
Circular Muscle Layer ◽  
Circular Layer ◽  
Longitudinal Layer

The electrical basis of propulsive contractions in the guinea pig choledochoduodenal junction (CDJ), which are triggered by distension, was investigated using intracellular microelectrode recording techniques. The isolated CDJ was placed in a continuously perfused tissue chamber at 37 degrees C. Membrane potential was recorded from smooth muscle cells in either the ampulla or in the upper CDJ (upper junction) regions, which were immobilized by pinning. Distension of the upper junction (20-30 s) by increasing intraductal hydrostatic pressure (mean elevation: 2.0 +/- 0.3 kPa, n = 13) triggered "transient depolarizations" (TDs: < 5 mV in amplitude and 2-5 s in duration) and action potentials in the circular muscle layer of the ampulla. The frequency of TDs in the ampulla was increased from 2.2 +/- 0.2 to 15.9 +/- 2.2 min-1 (n = 13) during distension. Simultaneous impalements of cells in the longitudinal and circular muscle layers in the ampulla revealed that subthreshold TDs in the circular layer were associated with an increased rate of action potential discharge in the longitudinal layer. Atropine (Atr; 1.4 x 10(-6) M) and tetrodotoxin (TTX; 3.1 x 10(-6) M blocked the distension-evoked increase in TD frequency, without affecting the frequency of ongoing TDs. The sulfated octapeptide of cholecystokinin (1-5 x 10(-8) M) increased the amplitude of TDs recorded in the circular muscle layer of the ampulla and increased action potential discharge rate. In separate recordings, radial stretch of the ampulla region increased the rate of discharge of action potentials in the smooth muscle of the upper junction.(ABSTRACT TRUNCATED AT 250 WORDS)

Electrical coupling of longitudinal and circular intestinal muscle

1984 ◽  
Vol 246 (5) ◽  
pp. G618-G626 ◽  
Author(s):  
L. Elden ◽  
A. Bortoff
Keyword(s):  
Longitudinal Muscle ◽  
Electrical Coupling ◽  
Circular Muscle ◽  
Muscle Cells ◽  
Methyl Blue ◽  
Current Spread ◽  
Hyperpolarizing Response ◽  
Partition Method ◽  
High Degree ◽  
Longitudinal Layer

Space constants (lambda) were determined for longitudinal-circular muscle strips of cat jejunum by the partition method. Pulses of hyperpolarizing current spread along the major axes of circular muscle cells. In the absence of electrical coupling lambda measured from the longitudinal side of the strips should have been approximately 20 times shorter than lambda measured from the circular side. Median values were found to be statistically the same, 2.4 mm for the longitudinal side (n = 13) and 2.9 mm for the circular (n = 25). Methyl blue, iontophoretically injected into cells on the longitudinal side after recording large hyperpolarizing responses, was found in muscle cells located superficially in the longitudinal layer. The radial lambda for longitudinal muscle, determined from the change in magnitude of the hyperpolarizing response as the microelectrode was advanced through the layer, was 0.27 mm. This is too large to cause differences in depth of recording to significantly affect the circumferential lambda in this layer. These data provide evidence for a high degree of electrical coupling between the two muscle layers of cat jejunum.

Excitatory and inhibitory neural regulation of canine pyloric smooth muscle

1990 ◽  
Vol 259 (1) ◽  
pp. G125-G133 ◽  
Author(s):  
F. Vogalis ◽  
K. M. Sanders
Keyword(s):  
Action Potentials ◽  
Slow Component ◽  
Circular Muscle ◽  
Muscle Layer ◽  
Slow Waves ◽  
Cross Sectional ◽  
Intrinsic Innervation ◽  
Circular Layer ◽  
Neuromuscular Apparatus ◽  
Excitatory Junction Potentials

Studies were performed to characterize the intrinsic innervation of the circular muscle layer of the canine pylorus. Cross-sectional strips of muscle were studied with intracellular recording techniques, and junction potentials were elicited with transmural nerve stimulation. Neurally mediated responses were recorded from cells at several points through the thickness of the circular layer. Excitatory junction potentials (EJPs) increased and inhibitory junction potentials (IJPs) decreased in amplitude with distance from the myenteric border of the circular muscle. Atropine blocked EJPs throughout the circular layer, demonstrating that excitatory inputs are primarily cholinergic. The gradient in IJP amplitude persisted after blockade of EJPs. Three components of IJPs were identified: 1) a fast, apamin-sensitive component that reached a peak and decayed within approximately 1 s; 2) a slower, apamin-insensitive component that reached a peak within 800 ms but decayed slowly over 5 s; and 3) a very slow component that reached a maximum in 7-10 s. Junctional potentials affected the pattern of myogenic electrical activity. Transmural stimulation could evoke premature slow waves in the myenteric portion of the circular layer but when excitatory inputs were blocked, IJPs greatly reduced the amplitude of slow waves. EJPs elicited action potentials in submucosal portion of circular muscles, and IJPs hyperpolarized these cells. The influence of intrinsic nerves on contractile patterns of pyloric muscles was also characterized. These data demonstrate that a neuromuscular apparatus exists within the gastroduodenal junction for 1) local regulation of slow waves and 2) independent control of the myenteric and submucosal regions of the circular layer.

scholarly journals Electrophysiological Studies of the Antrum Muscle Fibers of the Guinea Pig Stomach

1970 ◽  
Vol 55 (1) ◽  
pp. 48-62 ◽  
Author(s):  
H. Kuriyama ◽  
T. Osa ◽  
H. Tasaki
Keyword(s):  
Slow Wave ◽  
Longitudinal Muscle ◽  
Muscle Fibers ◽  
Circular Muscle ◽  
Slow Waves ◽  
The Other ◽  
Spike Generation ◽  
High K ◽  
Electrophysiological Studies ◽  
Guinea Pig Stomach

The membrane potentials of single smooth muscle fibers of various regions of the stomach were measured, and do not differ from those measured in intestinal muscle. Spontaneous slow waves with superimposed spikes could be recorded from the longitudinal and circular muscle of the antrum. The development of tension was preceded by spikes but often tension appeared only when the slow waves were generated. Contracture in high K solution developed at a critical membrane potential of -42 mv. MnCl2 blocked the spike generation, then lowered the amplitude of the slow wave. On the other hand, withdrawal of Na+, or addition of atropine and tetrodotoxin inhibited the generation of most of the slow waves but a spike could still be elicited by electrical stimulation. Prostigmine enhanced and prolonged the slow wave; acetylcholine depolarized the membrane without change in the frequency of the slow waves. Chronaxie for the spike generation in the longitudinal muscle of the antrum was 30 msec and conduction velocity was 1.2 cm/sec. The time constant of the foot of the propagated spike was 28 msec. The space constants measured from the longitudinal and circular muscles of the antrum were 1.1 mm and 1.4 mm, respectively.

Longitudinal contractions in the duodenum: their fluid-mechanical function

1975 ◽  
Vol 228 (6) ◽  
pp. 1887-1892 ◽  
Author(s):  
J Melville ◽  
E Macagno ◽  
J Christensen
Keyword(s):  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Muscle Layer ◽  
Slow Waves ◽  
Longitudinal Muscle Layer ◽  
Circular Muscle Layer ◽  
Model Flow ◽  
Displacement Wave ◽  
Marked Points

The hypothesis examined was that contractions of the longitudinal muscle layer occurin the duodenum which are independent of those of the circular muscle layer and that they induce flow of duodenal contents. A segment of opossum duodenum isolated in vitro was marked and photographed during periods of longitudinal muscle contraction, when the circular muscle layer appeared inactive. The prequency of longitudinal oscillation of the marked points was 20.5 cycles/min. The longitudinal displacement wave spread caudad with an average velocity of 3.27 cm/s. Frequency and velocity of electrical slow waves were determined in similiar duodenal segments. Slow-wave frquencywas 18.9 cycles/min. In a two-dimensional mechanical model, flow induced by simulatedlongitudinal muscle layer appear to be driven by the electrical slow waves of the duodenum. They are capable of inducing a pattern of flow in which ocntents flow betweenthe core and the periphery of the intestinal conduit.

Sign in / Sign up

Export Citation Format

Share Document