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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 |
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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. |
doi_str_mv | 10.1046/j.1365-2982.2003.00405.x |
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K. ; Bywater, R. A. R.</creator><creatorcontrib>Powell, A. K. ; Bywater, R. A. R.</creatorcontrib><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. 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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). 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.</description><subject>Anesthetics, Local - pharmacology</subject><subject>Animals</subject><subject>CMMCs</subject><subject>colon</subject><subject>enteric nervous system</subject><subject>Free Radical Scavengers - pharmacology</subject><subject>Ganglionic Blockers - pharmacology</subject><subject>Gastrointestinal Motility - physiology</subject><subject>Hexamethonium - pharmacology</subject><subject>ileum</subject><subject>Intestines - drug effects</subject><subject>Intestines - physiology</subject><subject>longitudinal muscle</subject><subject>Mice</subject><subject>Morphine - pharmacology</subject><subject>mouse</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - physiology</subject><subject>Myoelectric Complex, Migrating - drug effects</subject><subject>Myoelectric Complex, Migrating - physiology</subject><subject>Nifedipine - pharmacology</subject><subject>Nitric Oxide - metabolism</subject><subject>Organ Culture Techniques</subject><subject>Serotonin - pharmacology</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Vasodilator Agents - pharmacology</subject><issn>1350-1925</issn><issn>1365-2982</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkMtOwzAQRS0EoqXwCygrdgl-xY0RG1SeUks3sLYSZ1y5SuJiJ6L9e5K2gi2ruRqfmbEOQhHBCcFc3K4TwkQaU5nRhGLMEow5TpPtCRr_PpwOOcUxkTQdoYsQ1hhjQbk4RyNCp9mUMT5Gj4vO2wYi27QQWtvkVVTblc_7uIpq1zofaVdvKthCuIsq16xs25V7bui7Bpo2XKIzk1cBro51gj6fnz5mr_F8-fI2e5jHOiUkjYHlU8GgKKmmBeiCc0M1yRiWhpmCgClZyVJaSCFNwQlwxkAyELnQ2pSpYRN0c9i78e6r6_-rahs0VFXegOuCojijkjDZg9kB1N6F4MGojbd17neKYDUYVGs1iFKDKDUYVHuDatuPXh9vdEUN5d_gUVkP3B-Ab1vB7t-L1fti2Qf2A0ZJgQg</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Powell, A. K.</creator><creator>Bywater, R. A. R.</creator><general>Blackwell Science Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>200306</creationdate><title>Murine intestinal migrating motor complexes: longitudinal components</title><author>Powell, A. K. ; Bywater, R. A. R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5115-e3a763ebd2c2becb44f2c18309f3fb1efd3d352b969fb41e433e93e6a6ccfd5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Anesthetics, Local - pharmacology</topic><topic>Animals</topic><topic>CMMCs</topic><topic>colon</topic><topic>enteric nervous system</topic><topic>Free Radical Scavengers - pharmacology</topic><topic>Ganglionic Blockers - pharmacology</topic><topic>Gastrointestinal Motility - physiology</topic><topic>Hexamethonium - pharmacology</topic><topic>ileum</topic><topic>Intestines - drug effects</topic><topic>Intestines - physiology</topic><topic>longitudinal muscle</topic><topic>Mice</topic><topic>Morphine - pharmacology</topic><topic>mouse</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle, Smooth - drug effects</topic><topic>Muscle, Smooth - physiology</topic><topic>Myoelectric Complex, Migrating - drug effects</topic><topic>Myoelectric Complex, Migrating - physiology</topic><topic>Nifedipine - pharmacology</topic><topic>Nitric Oxide - metabolism</topic><topic>Organ Culture Techniques</topic><topic>Serotonin - pharmacology</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Powell, A. K.</creatorcontrib><creatorcontrib>Bywater, R. A. R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Neurogastroenterology and motility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Powell, A. K.</au><au>Bywater, R. A. 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. 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.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>12787334</pmid><doi>10.1046/j.1365-2982.2003.00405.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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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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