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Adiponectin and the regulation of gastric content volume in the newborn rat
BACKGROUND: Oral intake is dependent on the gastric ability to accommodate the food bolus. Comparatively, neonates have a smaller gastric capacity than adults and this may limit the volume of their milk intake. Yet, we previously reported that the newborn rat gastric milk volume is greatest after bi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433619/ https://www.ncbi.nlm.nih.gov/pubmed/34588752 http://dx.doi.org/10.3748/wjg.v27.i33.5566 |
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author | Wang, Huanhuan Esemu-Ezewu, Paul Pan, Jingyi Ivanovska, Julijana Gauda, Estelle B Belik, Jaques |
author_facet | Wang, Huanhuan Esemu-Ezewu, Paul Pan, Jingyi Ivanovska, Julijana Gauda, Estelle B Belik, Jaques |
author_sort | Wang, Huanhuan |
collection | PubMed |
description | BACKGROUND: Oral intake is dependent on the gastric ability to accommodate the food bolus. Comparatively, neonates have a smaller gastric capacity than adults and this may limit the volume of their milk intake. Yet, we previously reported that the newborn rat gastric milk volume is greatest after birth and, when normalized to body weight, decreases with postnatal age. Such age-dependent changes are not the result of intake differences, but greater gastric accommodation and reduced emptying rate. AIM: Hypothesizing that breastmilk-derived adiponectin is the factor regulating gastric accommodation in neonates, we comparatively evaluated its effects on the rat fundic muscle tone at different postnatal ages. METHODS: In freshly dispersed smooth muscle cells (SMC), we measured the adiponectin effect on the carbachol-induced length changes. RESULTS: Adiponectin significantly reduced the carbachol-stimulated SMC shortening independently of age. In the presence of the inhibitor iberiotoxin, the adiponectin effect on SMC shortening was suppressed, suggesting that it is mediated via large-conductance Ca(2+) sensitive K(+) channel activation. Lastly, we comparatively measured the newborn rat gastric milk curd adiponectin content in one- and two-week-old rats and found a 50% lower value in the latter. CONCLUSION: Adiponectin, a major component of breastmilk, downregulates fundic smooth muscle contraction potential, thus facilitating gastric volume accommodation. This rodent’s adaptive response maximizes breastmilk intake volume after birth. |
format | Online Article Text |
id | pubmed-8433619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-84336192021-09-28 Adiponectin and the regulation of gastric content volume in the newborn rat Wang, Huanhuan Esemu-Ezewu, Paul Pan, Jingyi Ivanovska, Julijana Gauda, Estelle B Belik, Jaques World J Gastroenterol Basic Study BACKGROUND: Oral intake is dependent on the gastric ability to accommodate the food bolus. Comparatively, neonates have a smaller gastric capacity than adults and this may limit the volume of their milk intake. Yet, we previously reported that the newborn rat gastric milk volume is greatest after birth and, when normalized to body weight, decreases with postnatal age. Such age-dependent changes are not the result of intake differences, but greater gastric accommodation and reduced emptying rate. AIM: Hypothesizing that breastmilk-derived adiponectin is the factor regulating gastric accommodation in neonates, we comparatively evaluated its effects on the rat fundic muscle tone at different postnatal ages. METHODS: In freshly dispersed smooth muscle cells (SMC), we measured the adiponectin effect on the carbachol-induced length changes. RESULTS: Adiponectin significantly reduced the carbachol-stimulated SMC shortening independently of age. In the presence of the inhibitor iberiotoxin, the adiponectin effect on SMC shortening was suppressed, suggesting that it is mediated via large-conductance Ca(2+) sensitive K(+) channel activation. Lastly, we comparatively measured the newborn rat gastric milk curd adiponectin content in one- and two-week-old rats and found a 50% lower value in the latter. CONCLUSION: Adiponectin, a major component of breastmilk, downregulates fundic smooth muscle contraction potential, thus facilitating gastric volume accommodation. This rodent’s adaptive response maximizes breastmilk intake volume after birth. Baishideng Publishing Group Inc 2021-09-07 2021-09-07 /pmc/articles/PMC8433619/ /pubmed/34588752 http://dx.doi.org/10.3748/wjg.v27.i33.5566 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Basic Study Wang, Huanhuan Esemu-Ezewu, Paul Pan, Jingyi Ivanovska, Julijana Gauda, Estelle B Belik, Jaques Adiponectin and the regulation of gastric content volume in the newborn rat |
title | Adiponectin and the regulation of gastric content volume in the newborn rat |
title_full | Adiponectin and the regulation of gastric content volume in the newborn rat |
title_fullStr | Adiponectin and the regulation of gastric content volume in the newborn rat |
title_full_unstemmed | Adiponectin and the regulation of gastric content volume in the newborn rat |
title_short | Adiponectin and the regulation of gastric content volume in the newborn rat |
title_sort | adiponectin and the regulation of gastric content volume in the newborn rat |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433619/ https://www.ncbi.nlm.nih.gov/pubmed/34588752 http://dx.doi.org/10.3748/wjg.v27.i33.5566 |
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