Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model
The enteric nervous system maturation occurs during embryonic life and continues after birth. Some prenatal events on the digestive tract such as intestinal atresia have been shown to dramatically alter this maturation. Thus, we developed a fetal rat model of intestinal atresia by surgically obstruc...
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Veröffentlicht in: | Neuroscience letters 2009-09, Vol.461 (2), p.126-130 |
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description | The enteric nervous system maturation occurs during embryonic life and continues after birth. Some prenatal events on the digestive tract such as intestinal atresia have been shown to dramatically alter this maturation. Thus, we developed a fetal rat model of intestinal atresia by surgically obstructing the small bowel at embryonic day E18. Fetuses were removed at day E21, and small bowels sections were examined by immuno-histochemistry. Synaptophysin and smooth muscle actin staining was used to define the cellular aspect. Labeling revealed marked alterations of the myenteric plexus in the lower extremity of the occluded small bowel. At day E21, the myenteric plexus of the lower part and the 2 muscle layers surrounding it, retained the staining pattern observed at day E17. This cellular pattern was classified as: immature (aspect at day E17) vs. mature (aspect of day E21) by 3 pathologists not familiar with the study. The number of samples with an immature cellular pattern at the lower end of the occluded bowel was different from that observed for the upper end (Mac Nemar test,
p
<
0.008). Our study suggests that a prenatal obstruction induces a maturation delay of the myenteric plexus downstream of the obstruction. This might be important for pediatric purposes. |
doi_str_mv | 10.1016/j.neulet.2009.06.009 |
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p
<
0.008). Our study suggests that a prenatal obstruction induces a maturation delay of the myenteric plexus downstream of the obstruction. This might be important for pediatric purposes.</description><identifier>ISSN: 0304-3940</identifier><identifier>EISSN: 1872-7972</identifier><identifier>DOI: 10.1016/j.neulet.2009.06.009</identifier><identifier>PMID: 19539706</identifier><identifier>CODEN: NELED5</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Actins ; Actins - metabolism ; Animals ; Biochemistry, Molecular Biology ; Biological and medical sciences ; Enteric nervous system ; Female ; Fetal Diseases ; Fetal Diseases - pathology ; Fundamental and applied biological sciences. Psychology ; Genetics ; Genomics ; Human genetics ; Immunohistochemistry ; Intestinal Atresia ; Intestinal Atresia - complications ; Intestinal Atresia - embryology ; Intestinal motility ; Intestinal Obstruction ; Intestinal Obstruction - complications ; Intestinal Obstruction - embryology ; Intestine, Small ; Intestine, Small - embryology ; Intestine, Small - innervation ; Life Sciences ; Molecular biology ; Muscle, Smooth ; Muscle, Smooth - embryology ; Muscle, Smooth - innervation ; Myenteric Plexus ; Myenteric Plexus - abnormalities ; Myenteric Plexus - embryology ; Neurobiology ; Neurons and Cognition ; Pregnancy ; Pregnancy Complications ; Pregnancy Complications - pathology ; Rat ; Rats ; Smooth muscle actin ; Synaptophysin ; Synaptophysin - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience letters, 2009-09, Vol.461 (2), p.126-130</ispartof><rights>2009 Elsevier Ireland Ltd</rights><rights>2009 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-f6ef42867eacecc4b0e9cb0774ac744069ecaffe9f440ee5fd54a5241f73d3f53</citedby><cites>FETCH-LOGICAL-c455t-f6ef42867eacecc4b0e9cb0774ac744069ecaffe9f440ee5fd54a5241f73d3f53</cites><orcidid>0000-0002-8352-0786</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S030439400900809X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21728275$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19539706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://unilim.hal.science/hal-00627950$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Fourcade, Laurent</creatorcontrib><creatorcontrib>Mousseau, Yoanne</creatorcontrib><creatorcontrib>Jaubert, Francis</creatorcontrib><creatorcontrib>Sturtz, Franck G.</creatorcontrib><title>Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model</title><title>Neuroscience letters</title><addtitle>Neurosci Lett</addtitle><description>The enteric nervous system maturation occurs during embryonic life and continues after birth. Some prenatal events on the digestive tract such as intestinal atresia have been shown to dramatically alter this maturation. Thus, we developed a fetal rat model of intestinal atresia by surgically obstructing the small bowel at embryonic day E18. Fetuses were removed at day E21, and small bowels sections were examined by immuno-histochemistry. Synaptophysin and smooth muscle actin staining was used to define the cellular aspect. Labeling revealed marked alterations of the myenteric plexus in the lower extremity of the occluded small bowel. At day E21, the myenteric plexus of the lower part and the 2 muscle layers surrounding it, retained the staining pattern observed at day E17. This cellular pattern was classified as: immature (aspect at day E17) vs. mature (aspect of day E21) by 3 pathologists not familiar with the study. The number of samples with an immature cellular pattern at the lower end of the occluded bowel was different from that observed for the upper end (Mac Nemar test,
p
<
0.008). Our study suggests that a prenatal obstruction induces a maturation delay of the myenteric plexus downstream of the obstruction. This might be important for pediatric purposes.</description><subject>Actins</subject><subject>Actins - metabolism</subject><subject>Animals</subject><subject>Biochemistry, Molecular Biology</subject><subject>Biological and medical sciences</subject><subject>Enteric nervous system</subject><subject>Female</subject><subject>Fetal Diseases</subject><subject>Fetal Diseases - pathology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics</subject><subject>Genomics</subject><subject>Human genetics</subject><subject>Immunohistochemistry</subject><subject>Intestinal Atresia</subject><subject>Intestinal Atresia - complications</subject><subject>Intestinal Atresia - embryology</subject><subject>Intestinal motility</subject><subject>Intestinal Obstruction</subject><subject>Intestinal Obstruction - complications</subject><subject>Intestinal Obstruction - embryology</subject><subject>Intestine, Small</subject><subject>Intestine, Small - embryology</subject><subject>Intestine, Small - innervation</subject><subject>Life Sciences</subject><subject>Molecular biology</subject><subject>Muscle, Smooth</subject><subject>Muscle, Smooth - embryology</subject><subject>Muscle, Smooth - innervation</subject><subject>Myenteric Plexus</subject><subject>Myenteric Plexus - abnormalities</subject><subject>Myenteric Plexus - embryology</subject><subject>Neurobiology</subject><subject>Neurons and Cognition</subject><subject>Pregnancy</subject><subject>Pregnancy Complications</subject><subject>Pregnancy Complications - pathology</subject><subject>Rat</subject><subject>Rats</subject><subject>Smooth muscle actin</subject><subject>Synaptophysin</subject><subject>Synaptophysin - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0304-3940</issn><issn>1872-7972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS1ERZfCP0AoF5A4JB07dry-IFUV0EqLeoEjsrzOWHjlxIudlPbf4yircoPTeEbfG73xI-QNhYYC7S4PzYhzwKlhAKqBrinlGdnQrWS1VJI9Jxtogdet4nBOXuZ8AABBBX9BzqkSrZLQbciPr484Tpi8rY4BH-ZcmVBaM_k45qqPv8c8JTRD5VIcKlMdE45mMqHyRZUnP5Zn3BdmtoukjAtU5NUQewyvyJkzIePrU70g3z9_-nZ9U-_uvtxeX-1qy4WYateh42zbSTQWreV7QGX3ICU3VnIOnUJrnEPlSoMoXC-4EYxTJ9u-daK9IB_WvT9N0MfkB5MedTRe31zt9DID6JhUAu5pYd-v7DHFX3O5QQ8-WwzBjBjnrDvJJaet-C_IKEi6FbKAfAVtijkndE8WKOglK33Qa1Z6yUpDV_yoInt72j_vB-z_ik7hFODdCTDZmuCSGa3PTxyjkm2ZXIx-XDksX3zvMelsPY4We5_QTrqP_t9O_gDgwbWn</recordid><startdate>20090918</startdate><enddate>20090918</enddate><creator>Fourcade, Laurent</creator><creator>Mousseau, Yoanne</creator><creator>Jaubert, Francis</creator><creator>Sturtz, Franck G.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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>7TK</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-8352-0786</orcidid></search><sort><creationdate>20090918</creationdate><title>Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model</title><author>Fourcade, Laurent ; Mousseau, Yoanne ; Jaubert, Francis ; Sturtz, Franck G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-f6ef42867eacecc4b0e9cb0774ac744069ecaffe9f440ee5fd54a5241f73d3f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Actins</topic><topic>Actins - metabolism</topic><topic>Animals</topic><topic>Biochemistry, Molecular Biology</topic><topic>Biological and medical sciences</topic><topic>Enteric nervous system</topic><topic>Female</topic><topic>Fetal Diseases</topic><topic>Fetal Diseases - pathology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics</topic><topic>Genomics</topic><topic>Human genetics</topic><topic>Immunohistochemistry</topic><topic>Intestinal Atresia</topic><topic>Intestinal Atresia - complications</topic><topic>Intestinal Atresia - embryology</topic><topic>Intestinal motility</topic><topic>Intestinal Obstruction</topic><topic>Intestinal Obstruction - complications</topic><topic>Intestinal Obstruction - embryology</topic><topic>Intestine, Small</topic><topic>Intestine, Small - embryology</topic><topic>Intestine, Small - innervation</topic><topic>Life Sciences</topic><topic>Molecular biology</topic><topic>Muscle, Smooth</topic><topic>Muscle, Smooth - embryology</topic><topic>Muscle, Smooth - innervation</topic><topic>Myenteric Plexus</topic><topic>Myenteric Plexus - abnormalities</topic><topic>Myenteric Plexus - embryology</topic><topic>Neurobiology</topic><topic>Neurons and Cognition</topic><topic>Pregnancy</topic><topic>Pregnancy Complications</topic><topic>Pregnancy Complications - pathology</topic><topic>Rat</topic><topic>Rats</topic><topic>Smooth muscle actin</topic><topic>Synaptophysin</topic><topic>Synaptophysin - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fourcade, Laurent</creatorcontrib><creatorcontrib>Mousseau, Yoanne</creatorcontrib><creatorcontrib>Jaubert, Francis</creatorcontrib><creatorcontrib>Sturtz, Franck G.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Neuroscience letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fourcade, Laurent</au><au>Mousseau, Yoanne</au><au>Jaubert, Francis</au><au>Sturtz, Franck G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model</atitle><jtitle>Neuroscience letters</jtitle><addtitle>Neurosci Lett</addtitle><date>2009-09-18</date><risdate>2009</risdate><volume>461</volume><issue>2</issue><spage>126</spage><epage>130</epage><pages>126-130</pages><issn>0304-3940</issn><eissn>1872-7972</eissn><coden>NELED5</coden><abstract>The enteric nervous system maturation occurs during embryonic life and continues after birth. Some prenatal events on the digestive tract such as intestinal atresia have been shown to dramatically alter this maturation. Thus, we developed a fetal rat model of intestinal atresia by surgically obstructing the small bowel at embryonic day E18. Fetuses were removed at day E21, and small bowels sections were examined by immuno-histochemistry. Synaptophysin and smooth muscle actin staining was used to define the cellular aspect. Labeling revealed marked alterations of the myenteric plexus in the lower extremity of the occluded small bowel. At day E21, the myenteric plexus of the lower part and the 2 muscle layers surrounding it, retained the staining pattern observed at day E17. This cellular pattern was classified as: immature (aspect at day E17) vs. mature (aspect of day E21) by 3 pathologists not familiar with the study. The number of samples with an immature cellular pattern at the lower end of the occluded bowel was different from that observed for the upper end (Mac Nemar test,
p
<
0.008). Our study suggests that a prenatal obstruction induces a maturation delay of the myenteric plexus downstream of the obstruction. This might be important for pediatric purposes.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>19539706</pmid><doi>10.1016/j.neulet.2009.06.009</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-8352-0786</orcidid></addata></record> |
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subjects | Actins Actins - metabolism Animals Biochemistry, Molecular Biology Biological and medical sciences Enteric nervous system Female Fetal Diseases Fetal Diseases - pathology Fundamental and applied biological sciences. Psychology Genetics Genomics Human genetics Immunohistochemistry Intestinal Atresia Intestinal Atresia - complications Intestinal Atresia - embryology Intestinal motility Intestinal Obstruction Intestinal Obstruction - complications Intestinal Obstruction - embryology Intestine, Small Intestine, Small - embryology Intestine, Small - innervation Life Sciences Molecular biology Muscle, Smooth Muscle, Smooth - embryology Muscle, Smooth - innervation Myenteric Plexus Myenteric Plexus - abnormalities Myenteric Plexus - embryology Neurobiology Neurons and Cognition Pregnancy Pregnancy Complications Pregnancy Complications - pathology Rat Rats Smooth muscle actin Synaptophysin Synaptophysin - metabolism Vertebrates: nervous system and sense organs |
title | Myenteric plexus alterations downstream from a prenatal intestinal obstruction in a rat model |
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