Evidence that stimulation of ghrelin receptors in the spinal cord initiates propulsive activity in the colon of the rat
Previous studies have failed to reveal an effect of the gastrointestinal peptide hormone ghrelin on colonic motility. In the present work, ghrelin was applied into the lumbo-sacral spinal cord in the region of defecation control centres, and a synthetic ghrelin receptor agonist, CP464709, which cros...
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Veröffentlicht in: | The Journal of physiology 2006-10, Vol.576 (1), p.329-338 |
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creator | Shimizu, Yasutake Chang, Ed C. Shafton, Anthony D. Ferens, Dorota M. Sanger, Gareth J. Witherington, Jason Furness, John B. |
description | Previous studies have failed to reveal an effect of the gastrointestinal peptide hormone ghrelin on colonic motility. In the
present work, ghrelin was applied into the lumbo-sacral spinal cord in the region of defecation control centres, and a synthetic
ghrelin receptor agonist, CP464709, which crosses the bloodâbrain barrier, was applied intravenously or into the lumbo-sacral
cord. Both ghrelin and CP464709 elicited propulsive contractions and emptying of the colon in anaesthetized rats. In conscious
rats, subcutaneous CP464709 caused fecal expulsion. The sites of action and nerve pathways involved in the stimulation of
the colon by ghrelin receptor activation were investigated in anaesthetized rats. Intrathecal application of CP464709 at L6âS1,
but not application at ponto-medullary levels or to the thoracic spinal cord, elicited propulsive contractions. The stimulation
evoked by intravenous CP464709 was prevented if the pelvic nerve outflows were severed, but not if the spinal cord was cut
rostral to the defecation centre at L6âS3. The response was also blocked by hexamethonium. When ghrelin, applied intrathecally,
was used to desensitize its receptors, the effect of intravenous CP464709 was blocked. CP464709 did not affect small intestine
motility or the amplitudes of visceromotor reflexes caused by colorectal distension. It is concluded that activation of ghrelin
receptors in the lumbo-sacral spinal cord triggers co-ordinated propulsive contractions that empty the colo-rectum. The pathways
through which these responses are generated pass out of the spinal cord via the pelvic nerves and cause propulsive contractions
through activation of enteric neurons. |
doi_str_mv | 10.1113/jphysiol.2006.116160 |
format | Article |
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present work, ghrelin was applied into the lumbo-sacral spinal cord in the region of defecation control centres, and a synthetic
ghrelin receptor agonist, CP464709, which crosses the bloodâbrain barrier, was applied intravenously or into the lumbo-sacral
cord. Both ghrelin and CP464709 elicited propulsive contractions and emptying of the colon in anaesthetized rats. In conscious
rats, subcutaneous CP464709 caused fecal expulsion. The sites of action and nerve pathways involved in the stimulation of
the colon by ghrelin receptor activation were investigated in anaesthetized rats. Intrathecal application of CP464709 at L6âS1,
but not application at ponto-medullary levels or to the thoracic spinal cord, elicited propulsive contractions. The stimulation
evoked by intravenous CP464709 was prevented if the pelvic nerve outflows were severed, but not if the spinal cord was cut
rostral to the defecation centre at L6âS3. The response was also blocked by hexamethonium. When ghrelin, applied intrathecally,
was used to desensitize its receptors, the effect of intravenous CP464709 was blocked. CP464709 did not affect small intestine
motility or the amplitudes of visceromotor reflexes caused by colorectal distension. It is concluded that activation of ghrelin
receptors in the lumbo-sacral spinal cord triggers co-ordinated propulsive contractions that empty the colo-rectum. The pathways
through which these responses are generated pass out of the spinal cord via the pelvic nerves and cause propulsive contractions
through activation of enteric neurons.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.2006.116160</identifier><identifier>PMID: 16873401</identifier><language>eng</language><publisher>Oxford, UK: The Physiological Society</publisher><subject>Alimentary ; Animals ; Colon - innervation ; Colon - physiology ; Defecation - drug effects ; Defecation - physiology ; Evoked Potentials - drug effects ; Evoked Potentials - physiology ; Ganglionic Blockers - pharmacology ; Gastrointestinal Motility - drug effects ; Gastrointestinal Motility - physiology ; Ghrelin ; Hexamethonium - pharmacology ; Male ; Motor Neurons - drug effects ; Motor Neurons - physiology ; Peptide Hormones - physiology ; Rats ; Rats, Sprague-Dawley ; Receptors, G-Protein-Coupled - agonists ; Receptors, G-Protein-Coupled - physiology ; Receptors, Ghrelin ; Spinal Cord - physiology</subject><ispartof>The Journal of physiology, 2006-10, Vol.576 (1), p.329-338</ispartof><rights>2006 The Journal of Physiology © 2006 The Physiological Society</rights><rights>2006 The Authors. Journal compilation © 2006 The Physiological Society 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5190-834d2770326d0ce067eb34333d7296940ac24a8edee0071bb8ca9eae065c883a3</citedby><cites>FETCH-LOGICAL-c5190-834d2770326d0ce067eb34333d7296940ac24a8edee0071bb8ca9eae065c883a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995628/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995628/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1416,1432,27923,27924,45573,45574,46408,46832,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16873401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimizu, Yasutake</creatorcontrib><creatorcontrib>Chang, Ed C.</creatorcontrib><creatorcontrib>Shafton, Anthony D.</creatorcontrib><creatorcontrib>Ferens, Dorota M.</creatorcontrib><creatorcontrib>Sanger, Gareth J.</creatorcontrib><creatorcontrib>Witherington, Jason</creatorcontrib><creatorcontrib>Furness, John B.</creatorcontrib><title>Evidence that stimulation of ghrelin receptors in the spinal cord initiates propulsive activity in the colon of the rat</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>Previous studies have failed to reveal an effect of the gastrointestinal peptide hormone ghrelin on colonic motility. In the
present work, ghrelin was applied into the lumbo-sacral spinal cord in the region of defecation control centres, and a synthetic
ghrelin receptor agonist, CP464709, which crosses the bloodâbrain barrier, was applied intravenously or into the lumbo-sacral
cord. Both ghrelin and CP464709 elicited propulsive contractions and emptying of the colon in anaesthetized rats. In conscious
rats, subcutaneous CP464709 caused fecal expulsion. The sites of action and nerve pathways involved in the stimulation of
the colon by ghrelin receptor activation were investigated in anaesthetized rats. Intrathecal application of CP464709 at L6âS1,
but not application at ponto-medullary levels or to the thoracic spinal cord, elicited propulsive contractions. The stimulation
evoked by intravenous CP464709 was prevented if the pelvic nerve outflows were severed, but not if the spinal cord was cut
rostral to the defecation centre at L6âS3. The response was also blocked by hexamethonium. When ghrelin, applied intrathecally,
was used to desensitize its receptors, the effect of intravenous CP464709 was blocked. CP464709 did not affect small intestine
motility or the amplitudes of visceromotor reflexes caused by colorectal distension. It is concluded that activation of ghrelin
receptors in the lumbo-sacral spinal cord triggers co-ordinated propulsive contractions that empty the colo-rectum. The pathways
through which these responses are generated pass out of the spinal cord via the pelvic nerves and cause propulsive contractions
through activation of enteric neurons.</description><subject>Alimentary</subject><subject>Animals</subject><subject>Colon - innervation</subject><subject>Colon - physiology</subject><subject>Defecation - drug effects</subject><subject>Defecation - physiology</subject><subject>Evoked Potentials - drug effects</subject><subject>Evoked Potentials - physiology</subject><subject>Ganglionic Blockers - pharmacology</subject><subject>Gastrointestinal Motility - drug effects</subject><subject>Gastrointestinal Motility - physiology</subject><subject>Ghrelin</subject><subject>Hexamethonium - pharmacology</subject><subject>Male</subject><subject>Motor Neurons - drug effects</subject><subject>Motor Neurons - physiology</subject><subject>Peptide Hormones - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, G-Protein-Coupled - agonists</subject><subject>Receptors, G-Protein-Coupled - physiology</subject><subject>Receptors, Ghrelin</subject><subject>Spinal Cord - physiology</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9vFCEYh4nR2G31GxjDSU9T-TMDw8XENLXaNNFDPROWeXeHhh1GYHYz3142s1V764m88PyeAD-E3lFySSnlnx7Gfk4u-EtGiChbggryAq1oLVQlpeIv0YoQxiouG3qGzlN6IIRyotRrdEZFK3lN6Aodrveug8ECzr3JOGW3m7zJLgw4bPC2j-DdgCNYGHOICZch94DT6AbjsQ2xK1suO5Mh4TGGcfLJ7QEbm93e5fkxYINflMchmvwGvdoYn-Dtab1Av75e3199q-5-3Hy_-nJX2YYqUrW87piUhDPREQtESFjzmnPeSaaEqomxrDYtdACESLpet9YoMAVsbNtywy_Q58U7TusddBaGHI3XY3Q7E2cdjNNPTwbX623Ya6pUI1hbBB9Oghh-T5Cy3rlkwXszQJiSFq0qv_kMkCouuKSsgPUC2hhSirD5extK9LFa_VitPlarl2pL7P3_L_kXOnVZALUAB-dhfpZU39_-pJIf5R-XbO-2_cFF0AudgnWQZ93IEtGcKf4HstXFHg</recordid><startdate>200610</startdate><enddate>200610</enddate><creator>Shimizu, Yasutake</creator><creator>Chang, Ed C.</creator><creator>Shafton, Anthony D.</creator><creator>Ferens, Dorota M.</creator><creator>Sanger, Gareth J.</creator><creator>Witherington, Jason</creator><creator>Furness, John B.</creator><general>The Physiological Society</general><general>Blackwell Publishing Ltd</general><general>Blackwell Science Inc</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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200610</creationdate><title>Evidence that stimulation of ghrelin receptors in the spinal cord initiates propulsive activity in the colon of the rat</title><author>Shimizu, Yasutake ; Chang, Ed C. ; Shafton, Anthony D. ; Ferens, Dorota M. ; Sanger, Gareth J. ; Witherington, Jason ; Furness, John B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5190-834d2770326d0ce067eb34333d7296940ac24a8edee0071bb8ca9eae065c883a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Alimentary</topic><topic>Animals</topic><topic>Colon - innervation</topic><topic>Colon - physiology</topic><topic>Defecation - drug effects</topic><topic>Defecation - physiology</topic><topic>Evoked Potentials - drug effects</topic><topic>Evoked Potentials - physiology</topic><topic>Ganglionic Blockers - pharmacology</topic><topic>Gastrointestinal Motility - drug effects</topic><topic>Gastrointestinal Motility - physiology</topic><topic>Ghrelin</topic><topic>Hexamethonium - pharmacology</topic><topic>Male</topic><topic>Motor Neurons - drug effects</topic><topic>Motor Neurons - physiology</topic><topic>Peptide Hormones - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, G-Protein-Coupled - agonists</topic><topic>Receptors, G-Protein-Coupled - physiology</topic><topic>Receptors, Ghrelin</topic><topic>Spinal Cord - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimizu, Yasutake</creatorcontrib><creatorcontrib>Chang, Ed C.</creatorcontrib><creatorcontrib>Shafton, Anthony D.</creatorcontrib><creatorcontrib>Ferens, Dorota M.</creatorcontrib><creatorcontrib>Sanger, Gareth J.</creatorcontrib><creatorcontrib>Witherington, Jason</creatorcontrib><creatorcontrib>Furness, John B.</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimizu, Yasutake</au><au>Chang, Ed C.</au><au>Shafton, Anthony D.</au><au>Ferens, Dorota M.</au><au>Sanger, Gareth J.</au><au>Witherington, Jason</au><au>Furness, John B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence that stimulation of ghrelin receptors in the spinal cord initiates propulsive activity in the colon of the rat</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2006-10</date><risdate>2006</risdate><volume>576</volume><issue>1</issue><spage>329</spage><epage>338</epage><pages>329-338</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>Previous studies have failed to reveal an effect of the gastrointestinal peptide hormone ghrelin on colonic motility. In the
present work, ghrelin was applied into the lumbo-sacral spinal cord in the region of defecation control centres, and a synthetic
ghrelin receptor agonist, CP464709, which crosses the bloodâbrain barrier, was applied intravenously or into the lumbo-sacral
cord. Both ghrelin and CP464709 elicited propulsive contractions and emptying of the colon in anaesthetized rats. In conscious
rats, subcutaneous CP464709 caused fecal expulsion. The sites of action and nerve pathways involved in the stimulation of
the colon by ghrelin receptor activation were investigated in anaesthetized rats. Intrathecal application of CP464709 at L6âS1,
but not application at ponto-medullary levels or to the thoracic spinal cord, elicited propulsive contractions. The stimulation
evoked by intravenous CP464709 was prevented if the pelvic nerve outflows were severed, but not if the spinal cord was cut
rostral to the defecation centre at L6âS3. The response was also blocked by hexamethonium. When ghrelin, applied intrathecally,
was used to desensitize its receptors, the effect of intravenous CP464709 was blocked. CP464709 did not affect small intestine
motility or the amplitudes of visceromotor reflexes caused by colorectal distension. It is concluded that activation of ghrelin
receptors in the lumbo-sacral spinal cord triggers co-ordinated propulsive contractions that empty the colo-rectum. The pathways
through which these responses are generated pass out of the spinal cord via the pelvic nerves and cause propulsive contractions
through activation of enteric neurons.</abstract><cop>Oxford, UK</cop><pub>The Physiological Society</pub><pmid>16873401</pmid><doi>10.1113/jphysiol.2006.116160</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; IngentaConnect Free/Open Access Journals; Wiley Online Library All Journals; PubMed Central |
subjects | Alimentary Animals Colon - innervation Colon - physiology Defecation - drug effects Defecation - physiology Evoked Potentials - drug effects Evoked Potentials - physiology Ganglionic Blockers - pharmacology Gastrointestinal Motility - drug effects Gastrointestinal Motility - physiology Ghrelin Hexamethonium - pharmacology Male Motor Neurons - drug effects Motor Neurons - physiology Peptide Hormones - physiology Rats Rats, Sprague-Dawley Receptors, G-Protein-Coupled - agonists Receptors, G-Protein-Coupled - physiology Receptors, Ghrelin Spinal Cord - physiology |
title | Evidence that stimulation of ghrelin receptors in the spinal cord initiates propulsive activity in the colon of the rat |
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