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
Hauptverfasser: Fourcade, Laurent, Mousseau, Yoanne, Jaubert, Francis, Sturtz, Franck G.
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Mousseau, Yoanne
Jaubert, Francis
Sturtz, Franck G.
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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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 &lt; 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. 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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 &lt; 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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source MEDLINE; ScienceDirect Journals (5 years ago - present)
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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