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Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days

Reportedly, proteins involved in lipid metabolism change significantly in the jejunal crypt cells of early-weaned piglets, but the exact lipid profile change remains uncertain. In the present study, 32 piglets weaned at 21 d of age were randomly divided into 4 groups with 8 replicates. The jejunal c...

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Autores principales: Shao, Yirui, Xiong, Xia, Wang, Kexing, Cheng, Pi, Zou, Lijun, Zhou, Jian, Qi, Ming, Yin, Yulong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489526/
https://www.ncbi.nlm.nih.gov/pubmed/36189377
http://dx.doi.org/10.1016/j.aninu.2022.07.001
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author Shao, Yirui
Xiong, Xia
Wang, Kexing
Cheng, Pi
Zou, Lijun
Zhou, Jian
Qi, Ming
Yin, Yulong
author_facet Shao, Yirui
Xiong, Xia
Wang, Kexing
Cheng, Pi
Zou, Lijun
Zhou, Jian
Qi, Ming
Yin, Yulong
author_sort Shao, Yirui
collection PubMed
description Reportedly, proteins involved in lipid metabolism change significantly in the jejunal crypt cells of early-weaned piglets, but the exact lipid profile change remains uncertain. In the present study, 32 piglets weaned at 21 d of age were randomly divided into 4 groups with 8 replicates. The jejunal crypt cells of a group of piglets on the post-weaning day (PWD) 1, 3, 7, and 14 were isolated per time point. Crypt cell lipid profiles were analyzed using ultra-high-performance liquid chromatography coupled with hybrid quadrupole time-of-flight mass spectrometry. This study showed that piglets suffered the greatest weaning stress on PWD 3 in terms of the lowest relative weight of the small intestine, the highest relative weight of the spleen, and the highest levels of malondialdehyde, cholesterol, and low-density lipoprotein cholesterol. The lipid profile of jejunal crypt cells including carnitine, sulfatide, sphingomyelin, hexosylceramide, and ceramide greatly changed after weaning, especially between PWD 3 and 14 (P < 0.05). The differential lipid species between these 2 d were mainly involved in the glycerophospholipid metabolism pathway. In addition, potential lipid biomarkers for weaning stress in crypt cells such as phosphatidylcholine (PC) (9:0/26:1), PC (17:0/18:2), carnitine (24:0), carnitine (22:0), sphingomyelin (d14:1/22:0), PC (P-18:0/18:4), phosphatidylethanolamine (P-16:0/20:4), phosphatidylinositol (15:1/24:4), and dihexosylceramide (d14:1/26:1) were identified. The changes in lipid profile might be related to the inflammation caused by early weaning. These findings might provide new therapeutical targets for intestinal dysfunctions caused by weaning stress.
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spelling pubmed-94895262022-09-30 Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days Shao, Yirui Xiong, Xia Wang, Kexing Cheng, Pi Zou, Lijun Zhou, Jian Qi, Ming Yin, Yulong Anim Nutr Original Research Article Reportedly, proteins involved in lipid metabolism change significantly in the jejunal crypt cells of early-weaned piglets, but the exact lipid profile change remains uncertain. In the present study, 32 piglets weaned at 21 d of age were randomly divided into 4 groups with 8 replicates. The jejunal crypt cells of a group of piglets on the post-weaning day (PWD) 1, 3, 7, and 14 were isolated per time point. Crypt cell lipid profiles were analyzed using ultra-high-performance liquid chromatography coupled with hybrid quadrupole time-of-flight mass spectrometry. This study showed that piglets suffered the greatest weaning stress on PWD 3 in terms of the lowest relative weight of the small intestine, the highest relative weight of the spleen, and the highest levels of malondialdehyde, cholesterol, and low-density lipoprotein cholesterol. The lipid profile of jejunal crypt cells including carnitine, sulfatide, sphingomyelin, hexosylceramide, and ceramide greatly changed after weaning, especially between PWD 3 and 14 (P < 0.05). The differential lipid species between these 2 d were mainly involved in the glycerophospholipid metabolism pathway. In addition, potential lipid biomarkers for weaning stress in crypt cells such as phosphatidylcholine (PC) (9:0/26:1), PC (17:0/18:2), carnitine (24:0), carnitine (22:0), sphingomyelin (d14:1/22:0), PC (P-18:0/18:4), phosphatidylethanolamine (P-16:0/20:4), phosphatidylinositol (15:1/24:4), and dihexosylceramide (d14:1/26:1) were identified. The changes in lipid profile might be related to the inflammation caused by early weaning. These findings might provide new therapeutical targets for intestinal dysfunctions caused by weaning stress. KeAi Publishing 2022-07-15 /pmc/articles/PMC9489526/ /pubmed/36189377 http://dx.doi.org/10.1016/j.aninu.2022.07.001 Text en © 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Shao, Yirui
Xiong, Xia
Wang, Kexing
Cheng, Pi
Zou, Lijun
Zhou, Jian
Qi, Ming
Yin, Yulong
Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
title Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
title_full Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
title_fullStr Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
title_full_unstemmed Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
title_short Early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
title_sort early weaning leads to the remodeling of lipid profile in piglet jejunal crypt cells during post-weaning days
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489526/
https://www.ncbi.nlm.nih.gov/pubmed/36189377
http://dx.doi.org/10.1016/j.aninu.2022.07.001
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