Separation of enkephalin-degrading enzymes from longitudinal muscle layer of bovine small intestine

1985 ◽  
Vol 34 (17) ◽  
pp. 3179-3183 ◽  
Author(s):  
Tadahiko Hazato ◽  
Mariko Shimamura ◽  
Ryoichi Kase ◽  
Mikio Iijima ◽  
Takashi Katayama
Keyword(s):  
Small Intestine ◽  
Longitudinal Muscle ◽  
Muscle Layer ◽  
Longitudinal Muscle Layer ◽  
Degrading Enzymes ◽  
Bovine Small Intestine

Responses of muscles of cat small intestine to autonomic nerve stimulation

1963 ◽  
Vol 204 (2) ◽  
pp. 352-358 ◽  
Author(s):  
Gordon L. Van Harn
Keyword(s):  
Small Intestine ◽  
Muscle Contraction ◽  
Nerve Stimulation ◽  
Sympathetic Nerve ◽  
Longitudinal Muscle ◽  
Muscle Layer ◽  
Slow Waves ◽  
Intraluminal Pressure ◽  
Sympathetic Nerve Stimulation ◽  
Longitudinal Muscle Layer

The externally recorded slow waves from the cat small intestine originate in the longitudinal muscle layer. In vitro the slow waves are recorded from all layers of the intestine if the segment is not immersed in a saline bath. When the longitudinal layer is removed from one region, the magnitude of the slow-wave potential in the other intestinal layers decreases as the distance from the intact longitudinal muscle layer is increased. An active intestine, in vivo, responds to sympathetic nerve stimulation by a hyperpolarization, cessation of spikes, and inhibition of muscle contraction. During inactivity of the intestine, either vagus or sympathetic nerve stimulation results in a depolarization, initiation of spikes, and muscle contraction. The nature of the response is influenced by the frequency of nerve stimulation and by the level of activity of the intestinal muscle, which is altered by intraluminal pressure changes. The effect of drugs on the response of the intestine to vagal and sympathetic nerve stimulation is such as to indicate that both inhibitory and excitatory nerve fibers are present in each of the autonomic nerves. The duration of the latent period of the response is long and highly variable, and a response requires 50–100 nerve volleys.

Proteolytic Inactivation of Substance P and Neurokinin A in the Longitudinal Muscle Layer of Guinea Pig Small Intestine

2006 ◽  
Vol 47 (3) ◽  
pp. 856-864 ◽  
Author(s):  
R. Nau ◽  
G. Schäfer ◽  
C. F. Deacon ◽  
T. Cole ◽  
D. V. Agoston ◽  
...  
Keyword(s):  
Small Intestine ◽  
Substance P ◽  
Guinea Pig ◽  
Longitudinal Muscle ◽  
Muscle Layer ◽  
Neurokinin A ◽  
Longitudinal Muscle Layer

Transmission of electrical activity through the gastroduodenal junction

1965 ◽  
Vol 208 (3) ◽  
pp. 531-536 ◽  
Author(s):  
Alex Bortoff ◽  
Noah Weg
Keyword(s):  
Small Intestine ◽  
Electrical Activity ◽  
Longitudinal Muscle ◽  
Muscle Layer ◽  
Slow Waves ◽  
Pyloric Antrum ◽  
Longitudinal Muscle Layer ◽  
Proximal Duodenum ◽  
Electrical And Mechanical Activities ◽  
Electrode Technique

The electrical and mechanical activities of the gastroduodenal junction were studied in isolated cat preparations, using the pressure-electrode technique. The spontaneous electrical activity of the pyloric antrum consists of periodic depolarizations, the configuration of which is somewhat more complex than that of comparable potentials recorded from the longitudinal muscle layer of the small intestine. Like their intestinal counterparts these antral slow waves may be associated with spike potentials which are thought to initiate contractions. The electrical activity at the gastroduodenal junction consists of a combination of antral and duodenal slow waves, sometimes accompanied by spike potentials. In the proximal duodenum, antral slow waves are represented by periodic depolarizations which may be associated with spike potentials followed by contractions. Because of the extension of the antral slow waves into the proximal duodenum, contractions initiated in the antrum may also extend into the proximal duodenum. It is concluded that the gastroduodenal junction is a transition zone, coordinating the electrical and corresponding mechanical activities of the antrum and proximal duodenum.

scholarly journals First reported case of per anal endoscopic myectomy (PAEM): A novel endoscopic technique for resection of lesions with severe fibrosis in the rectum

2017 ◽  
Vol 05 (03) ◽  
pp. E146-E150 ◽  
Author(s):  
David Rahni ◽  
Takashi Toyonaga ◽  
Yoshiko Ohara ◽  
Francesco Lombardo ◽  
Shinichi Baba ◽  
...  
Keyword(s):  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Muscle Layer ◽  
Rectal Tumor ◽  
Resection Margins ◽  
Submucosal Layer ◽  
Longitudinal Muscle Layer ◽  
Circular Muscle Layer ◽  
Tunneling Method ◽  
Severe Fibrosis

Background and study aims A 54-year-old man was diagnosed with a rectal tumor extending through the submucosal layer. The patient refused surgery and therefore endoscopic submucosal dissection (ESD) was pursued. The lesion exhibited the muscle retraction sign. After dissecting circumferentially around the fibrotic area by double tunneling method, a myotomy was performed through the internal circular muscle layer, creating a plane of dissection between the internal circular muscle layer and the external longitudinal muscle layer, and a myectomy was completed.The pathologic specimen verified T1b grade 1 sprouting adenocarcinoma with 4350 µm invasion into the submucosa with negative resection margins.

Sodium nitrite, a potent relaxant of rat stomach fundus: in vitro evidence

1998 ◽  
Vol 76 (10-11) ◽  
pp. 989-999 ◽  
Author(s):  
Michal Ceregrzyn ◽  
Tsuyoshi Ozaki ◽  
Atsukazu Kuwahara ◽  
Maria Wiechetek
Keyword(s):  
Methylene Blue ◽  
Potassium Channels ◽  
Guanylate Cyclase ◽  
Sodium Nitrite ◽  
Longitudinal Muscle ◽  
Circular Muscle ◽  
Muscle Layer ◽  
Rat Stomach ◽  
Longitudinal Muscle Layer ◽  
Stomach Fundus

The effects of sodium nitrite (0.1, 1, 10 mM) on mechanical activity of isolated rat stomach fundus muscle and the influence of guanylate cyclase activity inhibitor (methylene blue) and channel inhibitors (tetrodotoxin, charybdotoxin, apamin) were studied. Nitrite evoked dose-dependent relaxation in the longitudinal and circular muscle layers. The lowest effective concentration of sodium nitrite was 0.1 mM, which is comparable with the NOAEL (no observed adverse effect level). Tetrodotoxin (1 µM) markedly inhibited electrically induced contraction and rebound relaxation, but did not influence the nitrite-induced relaxation. Charybdotoxin (100 nM) decreased the relaxation evoked by 10 mM nitrite to 52.3 and 65.7% of control reaction in the circular and longitudinal muscle layer, respectively. Apamin (100 nM) did not influence the nitrite-induced relaxation. Methylene blue (10 µM) decreased relaxation induced by nitrite in the longitudinal and circular muscle layer, respectively, to 66.7 and 54.3% of the response to 1 mM nitrite alone. Relaxation induced by nitrite was decreased in the presence of L-cysteine (5 mM), and in the circular and longitudinal muscle layer reached 29.6 and 23.1%, respectively, of the response to 1 mM nitrite alone. We conclude that the relaxing effect of nitrite on gastric fundus results from its direct action on smooth muscle cells and probably the enteric nervous system is not involved in this action. The nitrite-elicited relaxation depends on activation of guanylate cyclase and high conductance Ca2+-activated potassium channels; however, activation of potassium channels might be a part of or might act in parallel with the mechanism involving the cyclic GMP system. Effects of nitrite observed in the presence of L-cysteine suggest that nitrosothiols are not responsible for nitrite-evoked activation of guanylate cyclase.Key words: nitrite, gastric motility, tetrodotoxin, methylene blue, charybdotoxin, L-cysteine.

Membrane currents recorded from a fragment of rabbit intestinal smooth muscle cell

1986 ◽  
Vol 251 (3) ◽  
pp. C335-C346 ◽  
Author(s):  
Y. Ohya ◽  
K. Terada ◽  
K. Kitamura ◽  
H. Kuriyama
Keyword(s):  
Smooth Muscle ◽  
Longitudinal Muscle ◽  
Outward Current ◽  
Ionic Currents ◽  
Muscle Layer ◽  
Dependent Manner ◽  
Rabbit Ileum ◽  
Longitudinal Muscle Layer ◽  
Inward Current ◽  
K Currents

Properties of ionic currents in smooth muscle membranes of the longitudinal muscle layer of the rabbit ileum were investigated using the single electrode voltage clamp method. In the present experiments, this method was applicable only to the smooth muscle ball (fragment) and not for the dispersed whole cell, because of incompleteness of the voltage clamping. A voltage step elicited a transient inward current followed by an outward current. This outward current was partly inhibited by Mn2+ or nisoldipine or by a reduction in the extracellular [Ca2+] ([Ca2+]o). Tetraethylammonium (TEA) reduced the delayed outward current in a dose-dependent manner, but 50 mM TEA did not produce a complete block of a residual current. When the pipette contained K+-free (Cs+ with TEA+) solution, the residual outward current was abolished. The inward current was elicited at -30 mV (holding potential of -60 mV) and reached the maximal value at +10 mV; the polarity was reversed at +60 mV. This inward current depended on the [Ca2+]o and was blocked by Mn2+ or nisoldipine. Ba2+ also permeated the membrane, and the inward current evoked by Ba2+ was also blocked by Mn2+ or nisoldipine. Reduction of [Na+]o in a solution containing 2.4 mM Ca2+ neither modified the current-voltage relation nor the decay of the inward current, but when [Ca2+]o was reduced to below 1 microM, Na+ permeated the membrane and was blocked by nisoldipine. In conclusion, ionic currents were recordable from the fragmented ball of the longitudinal muscle of rabbit ileum. There were at least two K+ currents as the outward current (Ca2+-dependent K+ and delayed K+ currents) and a Ca2+ current as the inward current. The property of the Ca2+ channel was similar to that observed with other preparations.

Motility of the small intestine: a look ahead

1985 ◽  
Vol 248 (5) ◽  
pp. G495-G500 ◽  
Author(s):  
J. R. Mathias ◽  
C. A. Sninsky
Keyword(s):  
Small Intestine ◽  
Action Potential ◽  
Muscle Layer ◽  
Control Mechanisms ◽  
Muscularis Mucosa ◽  
Longitudinal Muscle Layer ◽  
Look Ahead ◽  
Health And Disease ◽  
And Function ◽  
Contraction And Relaxation

Motility of the gastrointestinal tract has become an important discipline of gastroenterology. In this paper we review important observations made during the early development of this discipline, note the current level of knowledge, and look ahead to some of the questions we believe will be addressed in the near future. Is the slow wave the action potential equivalent of the longitudinal muscle layer? How does the migrating action potential complex interrelate with the migrating myoelectric complex--are they two separate complexes under different control mechanisms? How do the myenteric plexus neurons relate to these complexes? Does the muscularis mucosa control the contraction and relaxation of the villous tips? Is there a finite area in the small intestine that can function as the pacemaker? How important are substances within the lumen in controlling motility? Finally, we emphasize the importance of structure and function of the plexus neurons in motility studies. We also stress the importance of collaboration and a multidisciplinary approach for future understanding of the mechanisms of the small intestine in health and disease.

In vitro microelectrode study of the electrical properties of smooth muscle in equine ileum

2001 ◽  
Vol 149 (23) ◽  
pp. 707-711 ◽  
Author(s):  
N. P. H. Hudson ◽  
I. G. Mayhew ◽  
G. T. Pearson
Keyword(s):  
Smooth Muscle ◽  
Membrane Potential ◽  
Smooth Muscle Cells ◽  
Longitudinal Muscle ◽  
Muscle Cells ◽  
Muscle Layer ◽  
Potential Oscillations ◽  
Longitudinal Muscle Layer ◽  
Membrane Potential Oscillations

Intracellular microelectrode recordings were made from smooth muscle cells in cross-sectional preparations of equine ileum, superfused in vitro. Membrane potential oscillations and spike potentials were recorded in all preparations, but recordings were made more readily from cells in the longitudinal muscle layer than from cells in the circular layer. The mean (se) resting membrane potential (RMP) of smooth muscle cells in the longitudinal muscle layer was -51.9 (1.2) mV, and the membrane potential oscillations in this layer had a mean amplitude of 4.8 (0.4) mV, a frequency of 9.0 (0.1) cycles per minute and a duration of 5.8 (0.2) seconds. The membrane potential oscillations were preserved in the presence of tetrodotoxin. A waxing and waning pattern of membrane potential oscillation activity was observed. Nifedipine abolished the spiking contractile activity of the smooth muscle, did not abolish the membrane potential oscillations but did alter their temporal characteristics.

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