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Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter
BACKGROUND: This study aims to explore the role of lysophosphatidic acid receptors in the regulation mechanisms of contraction and relaxation of human lower esophageal sphincter. METHODS: Between July 2015 and March 2016, muscle strips were collected from a total of 30 patients (19 males, 11 females...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bayçınar Medical Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580277/ https://www.ncbi.nlm.nih.gov/pubmed/36303683 http://dx.doi.org/10.5606/tgkdc.dergisi.2022.22084 |
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author | Feng, Yong Wei, Wei Chen, Liang Liu, Jun-Feng |
author_facet | Feng, Yong Wei, Wei Chen, Liang Liu, Jun-Feng |
author_sort | Feng, Yong |
collection | PubMed |
description | BACKGROUND: This study aims to explore the role of lysophosphatidic acid receptors in the regulation mechanisms of contraction and relaxation of human lower esophageal sphincter. METHODS: Between July 2015 and March 2016, muscle strips were collected from a total of 30 patients (19 males, 11 females; mean age: 62±9.9 years; range, 52 to 68 years) who underwent an esophagectomy for mid-third esophageal carcinomas. The specimens were maintained in oxygenated Krebs solution. Muscle tension measurement technique in vitro was used to examine the effects of non-selective lysophosphatidic acid receptors agonists and antagonists, as well as selective lysophosphatidic acid receptors agonists on the clasp and sling fibers of human lower esophageal sphincter. RESULTS: The non-selective dopamine receptor agonist lysophosphatidic acid induced the contraction of the clasp and sling fibers of the human lower esophageal sphincter. The response induced by nonselective lysophosphatidic acid receptor agonist was inhibited completely by non-selective lysophosphatidic acid receptor antagonist. The selective lysophosphatidic acid 1 and 2 receptor agonist and the selective lysophosphatidic acid 3 receptor agonist induced a concentration-dependent contractile response of the clasp and sling fibers of the human lower esophageal sphincter. There was no significant difference in contraction rates between the clasp and sling fibers (p>0.05). CONCLUSION: This study indicates that lysophosphatidic acid regulates the lower esophageal sphincter is through its receptor; the lysophosphatidic acid receptors may be involved in the contractile response of the human lower esophageal sphincter. |
format | Online Article Text |
id | pubmed-9580277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Bayçınar Medical Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-95802772022-10-26 Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter Feng, Yong Wei, Wei Chen, Liang Liu, Jun-Feng Turk Gogus Kalp Damar Cerrahisi Derg Original Article BACKGROUND: This study aims to explore the role of lysophosphatidic acid receptors in the regulation mechanisms of contraction and relaxation of human lower esophageal sphincter. METHODS: Between July 2015 and March 2016, muscle strips were collected from a total of 30 patients (19 males, 11 females; mean age: 62±9.9 years; range, 52 to 68 years) who underwent an esophagectomy for mid-third esophageal carcinomas. The specimens were maintained in oxygenated Krebs solution. Muscle tension measurement technique in vitro was used to examine the effects of non-selective lysophosphatidic acid receptors agonists and antagonists, as well as selective lysophosphatidic acid receptors agonists on the clasp and sling fibers of human lower esophageal sphincter. RESULTS: The non-selective dopamine receptor agonist lysophosphatidic acid induced the contraction of the clasp and sling fibers of the human lower esophageal sphincter. The response induced by nonselective lysophosphatidic acid receptor agonist was inhibited completely by non-selective lysophosphatidic acid receptor antagonist. The selective lysophosphatidic acid 1 and 2 receptor agonist and the selective lysophosphatidic acid 3 receptor agonist induced a concentration-dependent contractile response of the clasp and sling fibers of the human lower esophageal sphincter. There was no significant difference in contraction rates between the clasp and sling fibers (p>0.05). CONCLUSION: This study indicates that lysophosphatidic acid regulates the lower esophageal sphincter is through its receptor; the lysophosphatidic acid receptors may be involved in the contractile response of the human lower esophageal sphincter. Bayçınar Medical Publishing 2022-07-29 /pmc/articles/PMC9580277/ /pubmed/36303683 http://dx.doi.org/10.5606/tgkdc.dergisi.2022.22084 Text en Copyright © 2022, Turkish Society of Cardiovascular Surgery https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Article Feng, Yong Wei, Wei Chen, Liang Liu, Jun-Feng Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
title | Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
title_full | Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
title_fullStr | Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
title_full_unstemmed | Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
title_short | Effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
title_sort | effects of lysophosphatidic acid on sling and clasp fibers of the human lower esophageal sphincter |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580277/ https://www.ncbi.nlm.nih.gov/pubmed/36303683 http://dx.doi.org/10.5606/tgkdc.dergisi.2022.22084 |
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