Swallowing induces sequential activation of esophageal longitudinal smooth muscle

1984 ◽  
Vol 247 (5) ◽  
pp. G515-G519 ◽  
Author(s):  
D. J. Sugarbaker ◽  
S. Rattan ◽  
R. K. Goyal
Keyword(s):  
Smooth Muscle ◽  
Muscle Contraction ◽  
Muscle Activation ◽  
Longitudinal Muscle ◽  
Vagal Stimulation ◽  
Circular Muscle ◽  
Mechanical Activity ◽  
Circular Smooth Muscle ◽  
Muscle Contract ◽  
Sequential Activation

We examined the mechanical activity of the longitudinal and circular muscles of the esophagus at three different levels (9, 5, and 1 cm above the lower esophageal sphincter) during peristalsis induced by swallows or vagal stimulation in anesthetized opossums with miniature strain gauges applied in the axis of muscle fibers. The onset of longitudinal muscle contraction occurred in an aboral sequence with swallows but simultaneously with vagal stimulation. The speed of longitudinal muscle activation with swallows was 7.6 +/- 1.7 cm/s. Circular muscle contraction occurred in an aboral sequence with vagal stimulation and swallowing with speeds of 4.1 +/- 0.8 and 2.3 +/- 0.1 cm/s, respectively. Longitudinal muscle contracted before the circular muscle at all sites. The duration of longitudinal muscle contraction increased aborally (P less than 0.05) with swallowing or vagal stimulation. These studies show that 1) during swallowing, esophageal longitudinal and circular smooth muscle contract in a sequential fashion, 2) the longitudinal muscle sequential contraction is due to central mechanisms, whereas circular muscle sequential contraction may be due to both central and peripheral mechanisms, and 3) peripheral neuromuscular mechanisms produce regional differences in the duration of longitudinal muscle contraction.

Mechanical and electrical activity of esophageal smooth muscle during peristalsis

1984 ◽  
Vol 246 (2) ◽  
pp. G145-G150 ◽  
Author(s):  
D. J. Sugarbaker ◽  
S. Rattan ◽  
R. K. Goyal
Keyword(s):  
Smooth Muscle ◽  
Membrane Potential ◽  
Longitudinal Muscle ◽  
Vagal Stimulation ◽  
Stimulus Frequency ◽  
Circular Muscle ◽  
Mechanical Activity ◽  
Pedicle Flap ◽  
Spike Burst ◽  
Suction Electrode

Mechanical events and membrane potential changes in response to evoked swallows and cervical vagal stimulation (10 and 40 Hz) were recorded in anesthetized opossums. Miniature strain-gauge transducers monitored the mechanical activity of the two layers. A suction electrode recorded from the intact esophagus, from a proximally based pedicle flap of longitudinal muscle (LM), and from circular muscle (CM). The onset of swallowing was marked by the onset of mylohyoid activity. During swallows LM contraction preceded CM contraction and was of longer duration. The latencies of LM and CM contraction were 1,980 +/- 38 and 2,250 +/- 101 ms, respectively. The durations of contraction of LM and CM were 5,590 +/- 260 and 3,330 +/- 67 ms, respectively. LM showed no hyperpolarization but showed depolarization and spike burst. The CM showed prompt hyperpolarization followed by depolarization and spike burst. Responses to vagal stimulation were qualitatively similar to swallows. The different components of the responses were quantitatively modified by changes in stimulus frequency. These studies show that, during peristalsis in response to swallows and vagal stimulation, 1) LM contraction occurs before CM and is of longer duration, and 2) unlike CM, LM does not hyperpolarize prior to depolarization.

Intercellular metabolic coupling in canine colon musculature

1995 ◽  
Vol 268 (6) ◽  
pp. C1492-C1502 ◽  
Author(s):  
L. Farraway ◽  
A. K. Ball ◽  
J. D. Huizinga
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Gap Junctions ◽  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Muscle Cells ◽  
Muscle Layer ◽  
Circular Smooth Muscle ◽  
Metabolic Coupling ◽  
Cells Of Cajal

Intercellular communication within the musculature of the canine colon was studied by examining the results of neurobiotin diffusion after injection of the tracer into smooth muscle cells at different locations within the muscle layer. Circular muscle at the submucosal surface, circular muscle adjacent to the myenteric plexus, and longitudinal muscle demonstrated different degrees of time-dependent tracer spread. At the submucosal surface, tracer spread was rapid, extensive, and unimpeded by connective tissue septa. At the myenteric side, tracer spread was also extensive but was much slower and confined to bundles of cells bordered by septa. In contrast to previous studies that suggest an absence of gap junctions at the myenteric side of the circular muscle, the neurobiotin spread indicates full metabolic coupling of all circular smooth muscle cells. Furthermore, in contrast to the belief that longitudinal muscle is completely devoid of gap junctions, tracer spread occurred between cells in this layer, although neurobiotin diffusion was very limited, nonuniform, and slow. In each area of the musculature studied, tracer spread was inhibited by octanol. When very long injection and wait times were implemented at the submucosal surface of the circular muscle, neurobiotin was observed to cross septa through the network of interstitial cells of Cajal, indicating that it is this network that provides communication between lamellae.

scholarly journals Jun kinase-induced overexpression of leukemia-associated Rho GEF (LARG) mediates sustained hypercontraction of longitudinal smooth muscle in inflammation

2014 ◽  
Vol 306 (12) ◽  
pp. C1129-C1141 ◽  
Author(s):  
Othman Al-Shboul ◽  
Ancy D. Nalli ◽  
Divya P. Kumar ◽  
Ruizhe Zhou ◽  
Sunila Mahavadi ◽  
...  
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Muscle Contraction ◽  
Longitudinal Muscle ◽  
Rho Kinase ◽  
Muscle Cells ◽  
Circular Smooth Muscle ◽  
Jun Kinase ◽  
Longitudinal Smooth Muscle ◽  
Tnf Α

The signaling pathways mediating sustained contraction of mouse colonic longitudinal smooth muscle and the mechanisms involved in hypercontractility of this muscle layer in response to cytokines and TNBS-induced colitis have not been fully explored. In control longitudinal smooth muscle cells, ACh acting via m3 receptors activated sequentially Gα12, RhoGEF (LARG), and the RhoA/Rho kinase pathway. There was abundant expression of MYPT1, minimal expression of CPI-17, and a notable absence of a PKC/CPI-17 pathway. LARG expression was increased in longitudinal muscle cells isolated from muscle strips cultured for 24 h with IL-1β or TNF-α or obtained from the colon of TNBS-treated mice. The increase in LARG expression was accompanied by a significant increase in ACh-stimulated Rho kinase and ZIP kinase activities, and sustained muscle contraction. The increase in LARG expression, Rho kinase and ZIP kinase activities, and sustained muscle contraction was abolished in cells pretreated with the Jun kinase inhibitor, SP600125 . Expression of the MLCP activator, telokin, and MLCP activity were also decreased in longitudinal muscle cells from TNBS-treated mice or from strips treated with IL-1β or TNF-α. In contrast, previous studies had shown that sustained contraction in circular smooth muscle is mediated by sequential activation of Gα13, p115RhoGEF, and dual RhoA-dependent pathways involving phosphorylation of MYPT1 and CPI-17. In colonic circular smooth muscle cells isolated from TNBS-treated mice or from strips treated with IL-1β or TNF-α, CPI-17 expression and sustained muscle contraction were decreased. The disparate changes in the two muscle layers contribute to intestinal dysmotility during inflammation.

Comparison of arteries with longitudinal and circular venous muscle from the rat

1977 ◽  
Vol 232 (2) ◽  
pp. H131-H139
Author(s):  
M. L. Cohen ◽  
K. S. Wiley
Keyword(s):  
Smooth Muscle ◽  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Rhythmic Activity ◽  
Vasoactive Agent ◽  
Circular Smooth Muscle ◽  
Maximal Force ◽  
Portal Veins ◽  
Muscle Responses

Rat portal, mesenteric, renal, and femoral veins possess functionally responsive circular and longitudinal smooth muscle layers in vitro. In contrast to the dominant rhythmically active longitudinal muscle of portal veins, rat longitudinal mesenteric veins lacked rhythmic activity and developed maximal force equivalent to that of mesenteric circular muscle. Renal and femoral veins exhibited predominantly circular smooth muscle responses. Rat veins must be subjected to between 1 g (renal and femoral) and 4 g (circular portal and mesenteric) of passive forse for optimal responsiveness. Contractile response to vasoactive agent including carbamylcholine, serotonin, and norepinephrine was quantitatively different among veins. Femoral veins developed greater maximal force in response to norepinephrine than to KCL, and the responses to norepinephrine were not altered by cocaine. In contrast, cocaine markedly potentiated responses to norepinephrine in portal, mesenteric, and renal veins and, to a lesser extent, in the mesenteric artery. These data demonstrate heterogeneity in rat venous tissue and suggest that neuronal innervation may markedly influence responses to norepinephrine in some, but not all, rat blood vessels.

Nitric oxide mediates outward potassium currents in opossum esophageal circular smooth muscle

1996 ◽  
Vol 270 (6) ◽  
pp. G932-G938 ◽  
Author(s):  
J. Jury ◽  
K. R. Boev ◽  
E. E. Daniel
Keyword(s):  
Nitric Oxide ◽  
Smooth Muscle ◽  
Circular Muscle ◽  
Outward Current ◽  
Equilibrium Potential ◽  
Patch Clamp Technique ◽  
Pipette Solution ◽  
Whole Cell ◽  
Circular Smooth Muscle ◽  
Outward Currents

Single smooth muscle cells from the opossum body circular muscle were isolated and whole cell currents were characterized by the whole cell patch-clamp technique. When the cells were held at -50 mV and depolarized to 70 mV in 20-mV increments, initial small inactivating inward currents were evoked (-30 to 30 mV) followed by larger sustained outward currents. Depolarization from a holding potential of -90 mV evoked an initial fast inactivating outward current sensitive to 4-aminopyridine but not to high levels of ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA). The outward currents reversed near K+ equilibrium potential and were abolished when KCl was replaced by CsCl in the pipette solution. The sustained outward current was inhibited by quinine and cesium. High EGTA in the pipette solution reduced but did not abolish the sustained outward currents, suggesting that both Ca(2+)-dependent and -independent currents were evoked. The nitric oxide (NO)-releasing agents Sin-1 and sodium nitroprusside increased outward K+ currents. High levels of EGTA in the pipette solution abolished the increase in outward current induced by Sin-1. The presence of cyclopiazonic acid, an inhibitor of the sarcoplasmic reticulum (SR) Ca2+ pump, blocked the effects of NO-releasing agents. We conclude that NO release activates K+ outward currents in opossum esophagus circular muscle, which may depend on Ca2+ release from the SR stores.

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.

Role of HERG-like K+ currents in opossum esophageal circular smooth muscle

1999 ◽  
Vol 277 (6) ◽  
pp. C1284-C1290 ◽  
Author(s):  
Hamid I. Akbarali ◽  
Hemant Thatte ◽  
Xue Dao He ◽  
Wayne R. Giles ◽  
Raj K. Goyal
Keyword(s):  
Smooth Muscle ◽  
Membrane Potential ◽  
Smooth Muscle Cells ◽  
Single Cells ◽  
Circular Muscle ◽  
Muscle Cells ◽  
Resting Membrane Potential ◽  
Channel Blockers ◽  
Circular Smooth Muscle ◽  
Inward Currents

An inwardly rectifying K+ conductance closely resembling the human ether-a-go-go-related gene (HERG) current was identified in single smooth muscle cells of opossum esophageal circular muscle. When cells were voltage clamped at 0 mV, in isotonic K+ solution (140 mM), step hyperpolarizations to −120 mV in 10-mV increments resulted in large inward currents that activated rapidly and then declined slowly (inactivated) during the test pulse in a time- and voltage- dependent fashion. The HERG K+ channel blockers E-4031 (1 μM), cisapride (1 μM), and La3+ (100 μM) strongly inhibited these currents as did millimolar concentrations of Ba2+. Immunoflourescence staining with anti-HERG antibody in single cells resulted in punctate staining at the sarcolemma. At membrane potentials near the resting membrane potential (−50 to −70 mV), this K+ conductance did not inactivate completely. In conventional microelectrode recordings, both E-4031 and cisapride depolarized tissue strips by 10 mV and also induced phasic contractions. In combination, these results provide direct experimental evidence for expression of HERG-like K+ currents in gastrointestinal smooth muscle cells and suggest that HERG plays an important role in modulating the resting membrane potential.

Electrophysiological analysis of responses to intrinsic nerves in circular muscle of opossum esophageal muscle

1988 ◽  
Vol 254 (1) ◽  
pp. G107-G116 ◽  
Author(s):  
R. Serio ◽  
E. E. Daniel
Keyword(s):  
Smooth Muscle ◽  
Circular Muscle ◽  
Electrical Field Stimulation ◽  
High Frequency Stimulation ◽  
Organ Bath ◽  
Circular Smooth Muscle ◽  
Time To Peak ◽  
Frequency Stimulation ◽  
Sucrose Gap ◽  
Cholinergic Agents

The nerve-mediated responses to electrical field stimulation (EFS) along the opossum esophageal circular smooth muscle were studied with the sucrose-gap recording technique. Strips from 1-2, 4-5, 7-8, and 10-11 cm above the lower esophageal sphincter were stimulated with short-train (300 ms) and long-train (3 s) durations at 29 degrees C. The response always consisted of a hyperpolarization [inhibitory junction potentials (IJP)] followed by an "off depolarization" often associated with spike potentials and mechanical contraction. Proximal to distal differences in the characteristics of the evoked responses were found, i.e., increasing amplitude, duration and time to peak hyperpolarization of the IJP, increasing latency, and amplitude of the off depolarization. Neither atropine, scopolamine, physostigmine, nor guanethidine altered these characteristics substantially. Circular strips of muscularis externa, studied in the organ bath at 37 degrees C using 10-s EFS trains at 5-40 pps, produced off contractions, enhanced by physostigmine and reduced by atropine. High-frequency stimulation occasionally initiated small persistent intrastimulus ("on") responses; some were sensitive to cholinergic agents, but there was no gradient in the delay in their onset. Atropine-insensitive and tetrodotoxin-potentiated transient on responses were occasionally detected. We conclude that only the noncholinergic, nonadrenergic innervation provides a functional intrinsic innervation directly to the opossum esophagus circular smooth muscle when nerves are activated by EFS.

Myogenic mechanism for peristalsis in the cat esophagus

1999 ◽  
Vol 277 (2) ◽  
pp. G306-G313 ◽  
Author(s):  
Harold G. Preiksaitis ◽  
Nicholas E. Diamant
Keyword(s):  
Muscle Contraction ◽  
Slow Wave ◽  
Circular Muscle ◽  
Smooth Muscle Contraction ◽  
Slow Waves ◽  
Mechanical Activity ◽  
Control Mechanisms ◽  
Slow Wave Oscillations

A myogenic control system (MCS) is a fundamental determinant of peristalsis in the stomach, small bowel, and colon. In the esophagus, attention has focused on neuronal control, the potential for a MCS receiving less attention. The myogenic properties of the cat esophagus were studied in vitro with and without nerves blocked by 1 μM TTX. Muscle contraction was recorded, while electrical activity was monitored by suction electrodes. Spontaneous, nonperistaltic, electrical, and mechanical activity was seen in the longitudinal muscle and persisted after TTX. Spontaneous circular muscle activity was minimal, and peristalsis was not observed without pharmacological activation. Direct electrical stimulation (ES) in the presence of bethanechol or tetraethylammonium chloride (TEA) produced slow-wave oscillations and spike potentials accompanying smooth muscle contraction that progressed along the esophagus. Increased concentrations of either drug in the presence of TTX produced slow waves and spike discharges, accompanied by peristalsis in 5 of 8 TEA- and 2 of 11 bethanechol-stimulated preparations without ES. Depolarization of the muscle by increasing K+ concentration also produced slow waves but no peristalsis. We conclude that the MCS in the esophagus requires specific activation and is manifest by slow-wave oscillations of the membrane potential, which appear to be necessary, but are not sufficient for myogenic peristalsis. In vivo, additional control mechanisms are likely supplied by nerves.

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