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A functional study on small intestinal smooth muscles in jejunal atresia

AIM: The present study was aimed to assess the contractile status of neonatal small intestinal smooth muscle of dilated pre-atretic part of intestinal atresia to resolve debatable issues related to mechanisms of persistent dysmotility after surgical repair. MATERIALS AND METHODS: A total of 34 longi...

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Autores principales: Tyagi, Preeti, Mandal, Maloy B., Gangopadhyay, Ajay N., Patne, Shashikant C. U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721123/
https://www.ncbi.nlm.nih.gov/pubmed/26862290
http://dx.doi.org/10.4103/0971-9261.164639
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author Tyagi, Preeti
Mandal, Maloy B.
Gangopadhyay, Ajay N.
Patne, Shashikant C. U.
author_facet Tyagi, Preeti
Mandal, Maloy B.
Gangopadhyay, Ajay N.
Patne, Shashikant C. U.
author_sort Tyagi, Preeti
collection PubMed
description AIM: The present study was aimed to assess the contractile status of neonatal small intestinal smooth muscle of dilated pre-atretic part of intestinal atresia to resolve debatable issues related to mechanisms of persistent dysmotility after surgical repair. MATERIALS AND METHODS: A total of 34 longitudinally sectioned strips were prepared from pre-atretic dilated part of freshly excised 8 jejunal atresia type III a cases. Spontaneous as well as acetylcholine- and histamine-induced contractions were recorded in vitro by using organ bath preparations. Chemically evoked contractions were further evaluated after application of atropine (muscarinic blocker), pheniramine (H1 blocker), and lignocaine (neuronal blocker) to ascertain receptors and neuronal involvement. Histological examinations of strips were made by using Masson trichrome stain to assess the fibrotic changes. RESULTS: All 34 strips, except four showed spontaneous contractions with mean frequency and amplitude of 5.49 ± 0.26/min and 24.41 ± 5.26 g/g wet tissue respectively. The response to ACh was nearly twice as compared to histamine for equimolar concentrations (100 μM). ACh (100 μM) induced contractions were attenuated (by 60%) by atropine. Histamine (100 μM)-induced contractions was blocked by pheniramine (0.32 μM) and lignocaine (4 μM) by 74% and 78%, respectively. Histopathological examination showed varying degree of fibrotic changes in muscle layers. CONCLUSIONS: Pre-atretic dilated part of jejunal atresia retains functional activity but with definitive histopathologic abnormalities. It is suggested that excision of a length of pre-atretic part and early stimulation of peristalsis by locally acting cholinomimetic or H1 agonist may help in reducing postoperative motility problems in atresia patients.
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spelling pubmed-47211232016-02-09 A functional study on small intestinal smooth muscles in jejunal atresia Tyagi, Preeti Mandal, Maloy B. Gangopadhyay, Ajay N. Patne, Shashikant C. U. J Indian Assoc Pediatr Surg Original Article AIM: The present study was aimed to assess the contractile status of neonatal small intestinal smooth muscle of dilated pre-atretic part of intestinal atresia to resolve debatable issues related to mechanisms of persistent dysmotility after surgical repair. MATERIALS AND METHODS: A total of 34 longitudinally sectioned strips were prepared from pre-atretic dilated part of freshly excised 8 jejunal atresia type III a cases. Spontaneous as well as acetylcholine- and histamine-induced contractions were recorded in vitro by using organ bath preparations. Chemically evoked contractions were further evaluated after application of atropine (muscarinic blocker), pheniramine (H1 blocker), and lignocaine (neuronal blocker) to ascertain receptors and neuronal involvement. Histological examinations of strips were made by using Masson trichrome stain to assess the fibrotic changes. RESULTS: All 34 strips, except four showed spontaneous contractions with mean frequency and amplitude of 5.49 ± 0.26/min and 24.41 ± 5.26 g/g wet tissue respectively. The response to ACh was nearly twice as compared to histamine for equimolar concentrations (100 μM). ACh (100 μM) induced contractions were attenuated (by 60%) by atropine. Histamine (100 μM)-induced contractions was blocked by pheniramine (0.32 μM) and lignocaine (4 μM) by 74% and 78%, respectively. Histopathological examination showed varying degree of fibrotic changes in muscle layers. CONCLUSIONS: Pre-atretic dilated part of jejunal atresia retains functional activity but with definitive histopathologic abnormalities. It is suggested that excision of a length of pre-atretic part and early stimulation of peristalsis by locally acting cholinomimetic or H1 agonist may help in reducing postoperative motility problems in atresia patients. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4721123/ /pubmed/26862290 http://dx.doi.org/10.4103/0971-9261.164639 Text en Copyright: © Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Tyagi, Preeti
Mandal, Maloy B.
Gangopadhyay, Ajay N.
Patne, Shashikant C. U.
A functional study on small intestinal smooth muscles in jejunal atresia
title A functional study on small intestinal smooth muscles in jejunal atresia
title_full A functional study on small intestinal smooth muscles in jejunal atresia
title_fullStr A functional study on small intestinal smooth muscles in jejunal atresia
title_full_unstemmed A functional study on small intestinal smooth muscles in jejunal atresia
title_short A functional study on small intestinal smooth muscles in jejunal atresia
title_sort functional study on small intestinal smooth muscles in jejunal atresia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4721123/
https://www.ncbi.nlm.nih.gov/pubmed/26862290
http://dx.doi.org/10.4103/0971-9261.164639
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