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Murine intestinal migrating motor complexes: longitudinal components

Spontaneous migrating contractions have been described in the circular muscle of the isolated mouse colon and terminal ileum, however, spontaneous events equivalent to these have not been reported in the longitudinal muscle. The longitudinal muscle shortenings in the colon and ileum, which are of si...

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Published in:Neurogastroenterology and motility 2003-06, Vol.15 (3), p.245-256
Main Authors: Powell, A. K., Bywater, R. A. R.
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Bywater, R. A. R.
description Spontaneous migrating contractions have been described in the circular muscle of the isolated mouse colon and terminal ileum, however, spontaneous events equivalent to these have not been reported in the longitudinal muscle. The longitudinal muscle shortenings in the colon and ileum, which are of similar form, frequency and pharmacology to the circular muscle colonic and ileal migrating motor complexes (CMMCs and IMMCs), are recorded in the present study. The spontaneous ileal and colonic longitudinal muscle shortenings appear to be neurally organized as they are abolished by tetrodotoxin (1 μmol L−1), hexamethonium (500 μmol L−1) and morphine (1 μmol L−1). Endogenously released nitric oxide slowed the frequency of spontaneous ileal and colonic longitudinal muscle shortenings and 5‐hydroxytryptamine increased their frequency. Hyoscine (1 μmol L−1) abolished longitudinal shortenings in the ileum and reduced the amplitude of longitudinal shortening by ∼44% in the colon. Shortenings were effectively abolished by nifedipine (1 μmol L−1). Surgical sectioning of the colon identified that each region of the colon contracted longitudinally in an independent fashion; the distal colon contracted to the greatest amplitude and lowest frequency. The longitudinal preparation is suitable to initially assess the actions of novel pharmacological agents on spontaneous, neurally coordinated, CMMCs and IMMCs in emptied isolated murine intestines.
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K.</creatorcontrib><creatorcontrib>Bywater, R. A. R.</creatorcontrib><title>Murine intestinal migrating motor complexes: longitudinal components</title><title>Neurogastroenterology and motility</title><addtitle>Neurogastroenterol Motil</addtitle><description>Spontaneous migrating contractions have been described in the circular muscle of the isolated mouse colon and terminal ileum, however, spontaneous events equivalent to these have not been reported in the longitudinal muscle. The longitudinal muscle shortenings in the colon and ileum, which are of similar form, frequency and pharmacology to the circular muscle colonic and ileal migrating motor complexes (CMMCs and IMMCs), are recorded in the present study. The spontaneous ileal and colonic longitudinal muscle shortenings appear to be neurally organized as they are abolished by tetrodotoxin (1 μmol L−1), hexamethonium (500 μmol L−1) and morphine (1 μmol L−1). 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R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Murine intestinal migrating motor complexes: longitudinal components</atitle><jtitle>Neurogastroenterology and motility</jtitle><addtitle>Neurogastroenterol Motil</addtitle><date>2003-06</date><risdate>2003</risdate><volume>15</volume><issue>3</issue><spage>245</spage><epage>256</epage><pages>245-256</pages><issn>1350-1925</issn><eissn>1365-2982</eissn><abstract>Spontaneous migrating contractions have been described in the circular muscle of the isolated mouse colon and terminal ileum, however, spontaneous events equivalent to these have not been reported in the longitudinal muscle. The longitudinal muscle shortenings in the colon and ileum, which are of similar form, frequency and pharmacology to the circular muscle colonic and ileal migrating motor complexes (CMMCs and IMMCs), are recorded in the present study. The spontaneous ileal and colonic longitudinal muscle shortenings appear to be neurally organized as they are abolished by tetrodotoxin (1 μmol L−1), hexamethonium (500 μmol L−1) and morphine (1 μmol L−1). Endogenously released nitric oxide slowed the frequency of spontaneous ileal and colonic longitudinal muscle shortenings and 5‐hydroxytryptamine increased their frequency. Hyoscine (1 μmol L−1) abolished longitudinal shortenings in the ileum and reduced the amplitude of longitudinal shortening by ∼44% in the colon. Shortenings were effectively abolished by nifedipine (1 μmol L−1). Surgical sectioning of the colon identified that each region of the colon contracted longitudinally in an independent fashion; the distal colon contracted to the greatest amplitude and lowest frequency. 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subjects Anesthetics, Local - pharmacology
Animals
CMMCs
colon
enteric nervous system
Free Radical Scavengers - pharmacology
Ganglionic Blockers - pharmacology
Gastrointestinal Motility - physiology
Hexamethonium - pharmacology
ileum
Intestines - drug effects
Intestines - physiology
longitudinal muscle
Mice
Morphine - pharmacology
mouse
Muscle Contraction - drug effects
Muscle Contraction - physiology
Muscle, Smooth - drug effects
Muscle, Smooth - physiology
Myoelectric Complex, Migrating - drug effects
Myoelectric Complex, Migrating - physiology
Nifedipine - pharmacology
Nitric Oxide - metabolism
Organ Culture Techniques
Serotonin - pharmacology
Tetrodotoxin - pharmacology
Vasodilator Agents - pharmacology
title Murine intestinal migrating motor complexes: longitudinal components
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