Melatonin as a modulator of the ileal brake mechanism

Objective The gastrointestinal tract represents the most important extrapineal source of melatonin. Intestinal melatonin release is induced by the ileal passage of nutrients and could play a part in the control of postprandial gut motility. The specific aim of this study was to determine the putativ...

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Veröffentlicht in:Scandinavian journal of gastroenterology 2005-05, Vol.40 (5), p.559-563
Hauptverfasser: Teresa Martín, Maria, Azpiroz, Fernando, Malagelada, Juan-R.
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container_issue 5
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container_title Scandinavian journal of gastroenterology
container_volume 40
creator Teresa Martín, Maria
Azpiroz, Fernando
Malagelada, Juan-R.
description Objective The gastrointestinal tract represents the most important extrapineal source of melatonin. Intestinal melatonin release is induced by the ileal passage of nutrients and could play a part in the control of postprandial gut motility. The specific aim of this study was to determine the putative role of melatonin in the "ileal brake" reflex, an important mechanism released by ileal lipids that regulates the gastric emptying of chyme. Material and methods Under general anaesthesia rats were fitted with ileal cannula exteriorized at the back of the neck. After a 1-week recovery, experiments were performed in conscious fasted animals. Rats were fed by gavage 1.5 ml casein hydrolyse plus 0.05% phenol red and either saline or Intralipid were continuously infused (2 ml/h) into the ileum. Gastric emptying was measured 50 min after ingestion by gastric lavage and determination of phenol red by spectrophotometry. The effects of melatonin (1 mg/kg) and melatonin antagonist S-22153 (dose-response study 0.2-25 mg/kg) were tested versus vehicle in paired experiments at 1-week intervals. Results Ileal infusion of lipids delayed gastric emptying. During ileal infusion of lipids, melatonin antagonist S-22153, but not melatonin, potentiated the delay in gastric emptying induced by the ileal brake mechanism. The inhibition of gastric emptying induced by S-22153 was dose related. Neither melatonin nor S-22153 had noticeable effects on gastric emptying during ileal infusion of saline. Conclusions Our data suggest that melatonin, released in response to ileal lipids, exerts a modulatory influence that decreases the inhibitory effects of the ileal brake on gastric emptying of nutrients.
doi_str_mv 10.1080/00365520510012316
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Intestinal melatonin release is induced by the ileal passage of nutrients and could play a part in the control of postprandial gut motility. The specific aim of this study was to determine the putative role of melatonin in the "ileal brake" reflex, an important mechanism released by ileal lipids that regulates the gastric emptying of chyme. Material and methods Under general anaesthesia rats were fitted with ileal cannula exteriorized at the back of the neck. After a 1-week recovery, experiments were performed in conscious fasted animals. Rats were fed by gavage 1.5 ml casein hydrolyse plus 0.05% phenol red and either saline or Intralipid were continuously infused (2 ml/h) into the ileum. Gastric emptying was measured 50 min after ingestion by gastric lavage and determination of phenol red by spectrophotometry. The effects of melatonin (1 mg/kg) and melatonin antagonist S-22153 (dose-response study 0.2-25 mg/kg) were tested versus vehicle in paired experiments at 1-week intervals. Results Ileal infusion of lipids delayed gastric emptying. During ileal infusion of lipids, melatonin antagonist S-22153, but not melatonin, potentiated the delay in gastric emptying induced by the ileal brake mechanism. The inhibition of gastric emptying induced by S-22153 was dose related. Neither melatonin nor S-22153 had noticeable effects on gastric emptying during ileal infusion of saline. Conclusions Our data suggest that melatonin, released in response to ileal lipids, exerts a modulatory influence that decreases the inhibitory effects of the ileal brake on gastric emptying of nutrients.</description><identifier>ISSN: 0036-5521</identifier><identifier>EISSN: 1502-7708</identifier><identifier>DOI: 10.1080/00365520510012316</identifier><identifier>PMID: 16036508</identifier><identifier>CODEN: SJGRA4</identifier><language>eng</language><publisher>Copenhagen: Informa UK Ltd</publisher><subject>Animals ; Biological and medical sciences ; Dose-Response Relationship, Drug ; Enterogastric reflexes ; Fat Emulsions, Intravenous - administration &amp; dosage ; Fundamental and applied biological sciences. Psychology ; Gastric Emptying ; Gastrointestinal Contents ; Gastrointestinal hormones ; ileal brake ; ileal lipids ; Ileum - physiology ; intestinal motility ; Male ; melatonin ; Melatonin - antagonists &amp; inhibitors ; Melatonin - physiology ; neural control ; Rats ; Rats, Sprague-Dawley ; Thiophenes - administration &amp; dosage ; Vertebrates: digestive system</subject><ispartof>Scandinavian journal of gastroenterology, 2005-05, Vol.40 (5), p.559-563</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-a26283397677366852c63fb47ce08b21ab22b0db1f9d51d8ecee2bb4f001058a3</citedby><cites>FETCH-LOGICAL-c434t-a26283397677366852c63fb47ce08b21ab22b0db1f9d51d8ecee2bb4f001058a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00365520510012316$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00365520510012316$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,59626,59732,60415,60521,61200,61235,61381,61416</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16756432$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16036508$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Teresa Martín, Maria</creatorcontrib><creatorcontrib>Azpiroz, Fernando</creatorcontrib><creatorcontrib>Malagelada, Juan-R.</creatorcontrib><title>Melatonin as a modulator of the ileal brake mechanism</title><title>Scandinavian journal of gastroenterology</title><addtitle>Scand J Gastroenterol</addtitle><description>Objective The gastrointestinal tract represents the most important extrapineal source of melatonin. Intestinal melatonin release is induced by the ileal passage of nutrients and could play a part in the control of postprandial gut motility. The specific aim of this study was to determine the putative role of melatonin in the "ileal brake" reflex, an important mechanism released by ileal lipids that regulates the gastric emptying of chyme. Material and methods Under general anaesthesia rats were fitted with ileal cannula exteriorized at the back of the neck. After a 1-week recovery, experiments were performed in conscious fasted animals. Rats were fed by gavage 1.5 ml casein hydrolyse plus 0.05% phenol red and either saline or Intralipid were continuously infused (2 ml/h) into the ileum. Gastric emptying was measured 50 min after ingestion by gastric lavage and determination of phenol red by spectrophotometry. The effects of melatonin (1 mg/kg) and melatonin antagonist S-22153 (dose-response study 0.2-25 mg/kg) were tested versus vehicle in paired experiments at 1-week intervals. Results Ileal infusion of lipids delayed gastric emptying. During ileal infusion of lipids, melatonin antagonist S-22153, but not melatonin, potentiated the delay in gastric emptying induced by the ileal brake mechanism. The inhibition of gastric emptying induced by S-22153 was dose related. Neither melatonin nor S-22153 had noticeable effects on gastric emptying during ileal infusion of saline. Conclusions Our data suggest that melatonin, released in response to ileal lipids, exerts a modulatory influence that decreases the inhibitory effects of the ileal brake on gastric emptying of nutrients.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Dose-Response Relationship, Drug</subject><subject>Enterogastric reflexes</subject><subject>Fat Emulsions, Intravenous - administration &amp; dosage</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastric Emptying</subject><subject>Gastrointestinal Contents</subject><subject>Gastrointestinal hormones</subject><subject>ileal brake</subject><subject>ileal lipids</subject><subject>Ileum - physiology</subject><subject>intestinal motility</subject><subject>Male</subject><subject>melatonin</subject><subject>Melatonin - antagonists &amp; inhibitors</subject><subject>Melatonin - physiology</subject><subject>neural control</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Thiophenes - administration &amp; dosage</subject><subject>Vertebrates: digestive system</subject><issn>0036-5521</issn><issn>1502-7708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUQIMoOj4-wI10o7vqTdI8Bt2I-IIRN7ouN2nKdEwbTVrEv7fDjKgIrgLJOZfcQ8ghhVMKGs4AuBSCgaAAlHEqN8iECmC5UqA3yWT5no8A3SG7KS0AQKhiuk12qFyaoCdEPDiPfeiaLsOUYdaGalhexCzUWT93WeMd-sxEfHFZ6-wcuya1-2SrRp_cwfrcI883109Xd_ns8fb-6nKW24IXfY5MMs35VEmluJRaMCt5bQplHWjDKBrGDFSG1tNK0Eo76xwzpqjHdUBo5HvkZDX3NYa3waW-bJtknffYuTCkUmqQSmo9gnQF2hhSiq4uX2PTYvwoKZTLVuWfVqNztB4-mNZV38Y6zggcrwFMFn0dsbNN-sEpIQvORu5ixTVdHWKL7yH6quzxw4f4JfH__nH-S5-Pwfu5xejKRRhiNwb-Z4tP73KT9A</recordid><startdate>20050501</startdate><enddate>20050501</enddate><creator>Teresa Martín, Maria</creator><creator>Azpiroz, Fernando</creator><creator>Malagelada, Juan-R.</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><general>Scandinavian University Press</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20050501</creationdate><title>Melatonin as a modulator of the ileal brake mechanism</title><author>Teresa Martín, Maria ; Azpiroz, Fernando ; Malagelada, Juan-R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-a26283397677366852c63fb47ce08b21ab22b0db1f9d51d8ecee2bb4f001058a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Dose-Response Relationship, Drug</topic><topic>Enterogastric reflexes</topic><topic>Fat Emulsions, Intravenous - administration &amp; dosage</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastric Emptying</topic><topic>Gastrointestinal Contents</topic><topic>Gastrointestinal hormones</topic><topic>ileal brake</topic><topic>ileal lipids</topic><topic>Ileum - physiology</topic><topic>intestinal motility</topic><topic>Male</topic><topic>melatonin</topic><topic>Melatonin - antagonists &amp; inhibitors</topic><topic>Melatonin - physiology</topic><topic>neural control</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Thiophenes - administration &amp; dosage</topic><topic>Vertebrates: digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Teresa Martín, Maria</creatorcontrib><creatorcontrib>Azpiroz, Fernando</creatorcontrib><creatorcontrib>Malagelada, Juan-R.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Scandinavian journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teresa Martín, Maria</au><au>Azpiroz, Fernando</au><au>Malagelada, Juan-R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Melatonin as a modulator of the ileal brake mechanism</atitle><jtitle>Scandinavian journal of gastroenterology</jtitle><addtitle>Scand J Gastroenterol</addtitle><date>2005-05-01</date><risdate>2005</risdate><volume>40</volume><issue>5</issue><spage>559</spage><epage>563</epage><pages>559-563</pages><issn>0036-5521</issn><eissn>1502-7708</eissn><coden>SJGRA4</coden><abstract>Objective The gastrointestinal tract represents the most important extrapineal source of melatonin. Intestinal melatonin release is induced by the ileal passage of nutrients and could play a part in the control of postprandial gut motility. The specific aim of this study was to determine the putative role of melatonin in the "ileal brake" reflex, an important mechanism released by ileal lipids that regulates the gastric emptying of chyme. Material and methods Under general anaesthesia rats were fitted with ileal cannula exteriorized at the back of the neck. After a 1-week recovery, experiments were performed in conscious fasted animals. Rats were fed by gavage 1.5 ml casein hydrolyse plus 0.05% phenol red and either saline or Intralipid were continuously infused (2 ml/h) into the ileum. Gastric emptying was measured 50 min after ingestion by gastric lavage and determination of phenol red by spectrophotometry. The effects of melatonin (1 mg/kg) and melatonin antagonist S-22153 (dose-response study 0.2-25 mg/kg) were tested versus vehicle in paired experiments at 1-week intervals. Results Ileal infusion of lipids delayed gastric emptying. During ileal infusion of lipids, melatonin antagonist S-22153, but not melatonin, potentiated the delay in gastric emptying induced by the ileal brake mechanism. The inhibition of gastric emptying induced by S-22153 was dose related. Neither melatonin nor S-22153 had noticeable effects on gastric emptying during ileal infusion of saline. Conclusions Our data suggest that melatonin, released in response to ileal lipids, exerts a modulatory influence that decreases the inhibitory effects of the ileal brake on gastric emptying of nutrients.</abstract><cop>Copenhagen</cop><cop>Oslo</cop><cop>Stockholm</cop><pub>Informa UK Ltd</pub><pmid>16036508</pmid><doi>10.1080/00365520510012316</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Taylor & Francis:Master (3349 titles); Taylor & Francis Medical Library - CRKN
subjects Animals
Biological and medical sciences
Dose-Response Relationship, Drug
Enterogastric reflexes
Fat Emulsions, Intravenous - administration & dosage
Fundamental and applied biological sciences. Psychology
Gastric Emptying
Gastrointestinal Contents
Gastrointestinal hormones
ileal brake
ileal lipids
Ileum - physiology
intestinal motility
Male
melatonin
Melatonin - antagonists & inhibitors
Melatonin - physiology
neural control
Rats
Rats, Sprague-Dawley
Thiophenes - administration & dosage
Vertebrates: digestive system
title Melatonin as a modulator of the ileal brake mechanism
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