The Role of 5-HT3 and 5-HT4 Receptors in the Adaptive Mechanism of Colonic Transit Following the Parasympathetic Denervation in Rats

Background Clinical studies show that disturbed colonic motility induced by extrinsic nerves damage is restored over time. We studied whether 5-HT3 and 5HT4 receptors are involved in mediating the adaptive mechanisms following parasympathetic denervation. Methods Parasympathetic denervation of the e...

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Veröffentlicht in:The Journal of surgical research 2011-12, Vol.171 (2), p.510-516
Hauptverfasser: Tong, Weidong, M.D, Kamiyama, Yoichi, M.D., Ph.D, Ridolfi, Tim J., M.D, Zietlow, Aaron, B.S, Zheng, Jun, M.D., Ph.D, Kosinski, Lauren, M.D, Ludwig, Kirk, M.D, Takahashi, Toku, M.D., Ph.D
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container_end_page 516
container_issue 2
container_start_page 510
container_title The Journal of surgical research
container_volume 171
creator Tong, Weidong, M.D
Kamiyama, Yoichi, M.D., Ph.D
Ridolfi, Tim J., M.D
Zietlow, Aaron, B.S
Zheng, Jun, M.D., Ph.D
Kosinski, Lauren, M.D
Ludwig, Kirk, M.D
Takahashi, Toku, M.D., Ph.D
description Background Clinical studies show that disturbed colonic motility induced by extrinsic nerves damage is restored over time. We studied whether 5-HT3 and 5HT4 receptors are involved in mediating the adaptive mechanisms following parasympathetic denervation. Methods Parasympathetic denervation of the entire colon was achieved by bilateral pelvic nerve transection and truncal vagotomy in rats. Colonic transit was measured by calculating the geometric center (GC) of51 Cr distribution. Expression of 5-HT3 and 5HT4 receptor mRNA was determined by real time RT-PCR. Results Parasympathetic denervation caused a significant delay in colonic transit (GC = 4.36) at postoperative day (POD) 1, compared with sham operation (GC = 6.31). Delayed transit was gradually restored by POD 7 (GC = 5.99) after the denervation. Restored colonic transit was antagonized by the administration of 5-HT3 and 5HT4 receptors antagonists at POD 7. 5-HT3 and 5HT4 receptors mRNA expression were significantly increased in the mucosal/submucosal layer at POD 3 or POD 7, whereas no significant difference was observed in the longitudinal muscle layers adherent with the myenteric plexus (LMMP). Conclusions It is suggested that up-regulation of 5-HT3 and 5-HT4 receptors expression in the mucosal/submucosal layer is involved to restore the delayed transit after the parasympathetic denervation in rats.
doi_str_mv 10.1016/j.jss.2010.05.002
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We studied whether 5-HT3 and 5HT4 receptors are involved in mediating the adaptive mechanisms following parasympathetic denervation. Methods Parasympathetic denervation of the entire colon was achieved by bilateral pelvic nerve transection and truncal vagotomy in rats. Colonic transit was measured by calculating the geometric center (GC) of51 Cr distribution. Expression of 5-HT3 and 5HT4 receptor mRNA was determined by real time RT-PCR. Results Parasympathetic denervation caused a significant delay in colonic transit (GC = 4.36) at postoperative day (POD) 1, compared with sham operation (GC = 6.31). Delayed transit was gradually restored by POD 7 (GC = 5.99) after the denervation. Restored colonic transit was antagonized by the administration of 5-HT3 and 5HT4 receptors antagonists at POD 7. 5-HT3 and 5HT4 receptors mRNA expression were significantly increased in the mucosal/submucosal layer at POD 3 or POD 7, whereas no significant difference was observed in the longitudinal muscle layers adherent with the myenteric plexus (LMMP). Conclusions It is suggested that up-regulation of 5-HT3 and 5-HT4 receptors expression in the mucosal/submucosal layer is involved to restore the delayed transit after the parasympathetic denervation in rats.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2010.05.002</identifier><identifier>PMID: 20691988</identifier><identifier>CODEN: JSGRA2</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>5-HT3 receptor ; 5-HT4 receptor ; Adaptation, Physiological - physiology ; Animals ; Biological and medical sciences ; colon ; Colon - innervation ; Colon - physiology ; denervation ; Gastrointestinal Motility - drug effects ; Gastrointestinal Motility - physiology ; General aspects ; Intestinal Mucosa - innervation ; Intestinal Mucosa - physiology ; Male ; Medical sciences ; Myenteric Plexus - physiology ; Nerve Regeneration - physiology ; Parasympathectomy ; parasympathetic ; Parasympathetic Nervous System - physiology ; Rats ; Rats, Sprague-Dawley ; Receptors, Serotonin, 5-HT3 - genetics ; Receptors, Serotonin, 5-HT3 - physiology ; Receptors, Serotonin, 5-HT4 - genetics ; Receptors, Serotonin, 5-HT4 - physiology ; RNA, Messenger - metabolism ; Serotonin 5-HT3 Receptor Antagonists - pharmacology ; Serotonin 5-HT4 Receptor Antagonists - pharmacology ; Surgery ; Up-Regulation - physiology</subject><ispartof>The Journal of surgical research, 2011-12, Vol.171 (2), p.510-516</ispartof><rights>2010</rights><rights>2015 INIST-CNRS</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c601t-6c406a603788e080b04f8a25e2cab6204a730b532b2bdc9cba9dade0044de72d3</citedby><cites>FETCH-LOGICAL-c601t-6c406a603788e080b04f8a25e2cab6204a730b532b2bdc9cba9dade0044de72d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S002248041000452X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=25229832$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20691988$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tong, Weidong, M.D</creatorcontrib><creatorcontrib>Kamiyama, Yoichi, M.D., Ph.D</creatorcontrib><creatorcontrib>Ridolfi, Tim J., M.D</creatorcontrib><creatorcontrib>Zietlow, Aaron, B.S</creatorcontrib><creatorcontrib>Zheng, Jun, M.D., Ph.D</creatorcontrib><creatorcontrib>Kosinski, Lauren, M.D</creatorcontrib><creatorcontrib>Ludwig, Kirk, M.D</creatorcontrib><creatorcontrib>Takahashi, Toku, M.D., Ph.D</creatorcontrib><title>The Role of 5-HT3 and 5-HT4 Receptors in the Adaptive Mechanism of Colonic Transit Following the Parasympathetic Denervation in Rats</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Background Clinical studies show that disturbed colonic motility induced by extrinsic nerves damage is restored over time. We studied whether 5-HT3 and 5HT4 receptors are involved in mediating the adaptive mechanisms following parasympathetic denervation. Methods Parasympathetic denervation of the entire colon was achieved by bilateral pelvic nerve transection and truncal vagotomy in rats. Colonic transit was measured by calculating the geometric center (GC) of51 Cr distribution. Expression of 5-HT3 and 5HT4 receptor mRNA was determined by real time RT-PCR. Results Parasympathetic denervation caused a significant delay in colonic transit (GC = 4.36) at postoperative day (POD) 1, compared with sham operation (GC = 6.31). Delayed transit was gradually restored by POD 7 (GC = 5.99) after the denervation. Restored colonic transit was antagonized by the administration of 5-HT3 and 5HT4 receptors antagonists at POD 7. 5-HT3 and 5HT4 receptors mRNA expression were significantly increased in the mucosal/submucosal layer at POD 3 or POD 7, whereas no significant difference was observed in the longitudinal muscle layers adherent with the myenteric plexus (LMMP). 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Kamiyama, Yoichi, M.D., Ph.D ; Ridolfi, Tim J., M.D ; Zietlow, Aaron, B.S ; Zheng, Jun, M.D., Ph.D ; Kosinski, Lauren, M.D ; Ludwig, Kirk, M.D ; Takahashi, Toku, M.D., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c601t-6c406a603788e080b04f8a25e2cab6204a730b532b2bdc9cba9dade0044de72d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>5-HT3 receptor</topic><topic>5-HT4 receptor</topic><topic>Adaptation, Physiological - physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>colon</topic><topic>Colon - innervation</topic><topic>Colon - physiology</topic><topic>denervation</topic><topic>Gastrointestinal Motility - drug effects</topic><topic>Gastrointestinal Motility - physiology</topic><topic>General aspects</topic><topic>Intestinal Mucosa - innervation</topic><topic>Intestinal Mucosa - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myenteric Plexus - physiology</topic><topic>Nerve Regeneration - physiology</topic><topic>Parasympathectomy</topic><topic>parasympathetic</topic><topic>Parasympathetic Nervous System - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Serotonin, 5-HT3 - genetics</topic><topic>Receptors, Serotonin, 5-HT3 - physiology</topic><topic>Receptors, Serotonin, 5-HT4 - genetics</topic><topic>Receptors, Serotonin, 5-HT4 - physiology</topic><topic>RNA, Messenger - metabolism</topic><topic>Serotonin 5-HT3 Receptor Antagonists - pharmacology</topic><topic>Serotonin 5-HT4 Receptor Antagonists - pharmacology</topic><topic>Surgery</topic><topic>Up-Regulation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tong, Weidong, M.D</creatorcontrib><creatorcontrib>Kamiyama, Yoichi, M.D., Ph.D</creatorcontrib><creatorcontrib>Ridolfi, Tim J., M.D</creatorcontrib><creatorcontrib>Zietlow, Aaron, B.S</creatorcontrib><creatorcontrib>Zheng, Jun, M.D., Ph.D</creatorcontrib><creatorcontrib>Kosinski, Lauren, M.D</creatorcontrib><creatorcontrib>Ludwig, Kirk, M.D</creatorcontrib><creatorcontrib>Takahashi, Toku, M.D., Ph.D</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of surgical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tong, Weidong, M.D</au><au>Kamiyama, Yoichi, M.D., Ph.D</au><au>Ridolfi, Tim J., M.D</au><au>Zietlow, Aaron, B.S</au><au>Zheng, Jun, M.D., Ph.D</au><au>Kosinski, Lauren, M.D</au><au>Ludwig, Kirk, M.D</au><au>Takahashi, Toku, M.D., Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Role of 5-HT3 and 5-HT4 Receptors in the Adaptive Mechanism of Colonic Transit Following the Parasympathetic Denervation in Rats</atitle><jtitle>The Journal of surgical research</jtitle><addtitle>J Surg Res</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>171</volume><issue>2</issue><spage>510</spage><epage>516</epage><pages>510-516</pages><issn>0022-4804</issn><eissn>1095-8673</eissn><coden>JSGRA2</coden><abstract>Background Clinical studies show that disturbed colonic motility induced by extrinsic nerves damage is restored over time. We studied whether 5-HT3 and 5HT4 receptors are involved in mediating the adaptive mechanisms following parasympathetic denervation. Methods Parasympathetic denervation of the entire colon was achieved by bilateral pelvic nerve transection and truncal vagotomy in rats. Colonic transit was measured by calculating the geometric center (GC) of51 Cr distribution. Expression of 5-HT3 and 5HT4 receptor mRNA was determined by real time RT-PCR. Results Parasympathetic denervation caused a significant delay in colonic transit (GC = 4.36) at postoperative day (POD) 1, compared with sham operation (GC = 6.31). Delayed transit was gradually restored by POD 7 (GC = 5.99) after the denervation. Restored colonic transit was antagonized by the administration of 5-HT3 and 5HT4 receptors antagonists at POD 7. 5-HT3 and 5HT4 receptors mRNA expression were significantly increased in the mucosal/submucosal layer at POD 3 or POD 7, whereas no significant difference was observed in the longitudinal muscle layers adherent with the myenteric plexus (LMMP). Conclusions It is suggested that up-regulation of 5-HT3 and 5-HT4 receptors expression in the mucosal/submucosal layer is involved to restore the delayed transit after the parasympathetic denervation in rats.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20691988</pmid><doi>10.1016/j.jss.2010.05.002</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects 5-HT3 receptor
5-HT4 receptor
Adaptation, Physiological - physiology
Animals
Biological and medical sciences
colon
Colon - innervation
Colon - physiology
denervation
Gastrointestinal Motility - drug effects
Gastrointestinal Motility - physiology
General aspects
Intestinal Mucosa - innervation
Intestinal Mucosa - physiology
Male
Medical sciences
Myenteric Plexus - physiology
Nerve Regeneration - physiology
Parasympathectomy
parasympathetic
Parasympathetic Nervous System - physiology
Rats
Rats, Sprague-Dawley
Receptors, Serotonin, 5-HT3 - genetics
Receptors, Serotonin, 5-HT3 - physiology
Receptors, Serotonin, 5-HT4 - genetics
Receptors, Serotonin, 5-HT4 - physiology
RNA, Messenger - metabolism
Serotonin 5-HT3 Receptor Antagonists - pharmacology
Serotonin 5-HT4 Receptor Antagonists - pharmacology
Surgery
Up-Regulation - physiology
title The Role of 5-HT3 and 5-HT4 Receptors in the Adaptive Mechanism of Colonic Transit Following the Parasympathetic Denervation in Rats
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