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Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep
OBJECTIVE: Fetal cardiopulmonary bypass (CPB) is essential to fetal heart surgery, while its development is limited by vital organ dysfunction after CPB. Studying organ metabolism may help to solve this problem. The objective of this study was to describe the tissue-specific metabolic fingerprints o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791045/ https://www.ncbi.nlm.nih.gov/pubmed/36578834 http://dx.doi.org/10.3389/fcvm.2022.1009165 |
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author | Wu, Wentao Teng, Yun Tian, Miao Huang, Bingxin Deng, Yuhang Li, Huili Yuan, Haiyun Chen, Jimei Li, Xiaohong Zhou, Chengbin |
author_facet | Wu, Wentao Teng, Yun Tian, Miao Huang, Bingxin Deng, Yuhang Li, Huili Yuan, Haiyun Chen, Jimei Li, Xiaohong Zhou, Chengbin |
author_sort | Wu, Wentao |
collection | PubMed |
description | OBJECTIVE: Fetal cardiopulmonary bypass (CPB) is essential to fetal heart surgery, while its development is limited by vital organ dysfunction after CPB. Studying organ metabolism may help to solve this problem. The objective of this study was to describe the tissue-specific metabolic fingerprints of fetal sheep under CPB and to associate them with organ functions. METHODS: Ten pregnant ewes at 90–120 days of gestation were randomly divided into two groups. The bypass group underwent a 1-h fetal CPB, whereas the control group underwent only a fetal sternotomy. During bypass, echocardiography, blood gases, and blood biochemistry were measured. After bypass, lambs were sacrificed, and tissues of the heart, liver, brain, kidney, and placenta were harvested. The metabolites extracted from these tissues were analyzed using non-targeted metabolomics based on liquid chromatography-mass spectrometry techniques. RESULTS: All tissues except the placenta displayed significant metabolic changes, and the fetal heart displayed obvious functional changes. Fetal sheep that underwent CPB had common and tissue-specific metabolic signatures. These changes can be attributed to dysregulated lipid metabolism, altered amino acid metabolism, and the accumulation of plasticizer metabolism. CONCLUSION: Fetal CPB causes tissue-specific metabolic changes in fetal sheep. Studying these metabolic changes, especially cardiac metabolism, is of great significance for the study of fetal CPB. |
format | Online Article Text |
id | pubmed-9791045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97910452022-12-27 Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep Wu, Wentao Teng, Yun Tian, Miao Huang, Bingxin Deng, Yuhang Li, Huili Yuan, Haiyun Chen, Jimei Li, Xiaohong Zhou, Chengbin Front Cardiovasc Med Cardiovascular Medicine OBJECTIVE: Fetal cardiopulmonary bypass (CPB) is essential to fetal heart surgery, while its development is limited by vital organ dysfunction after CPB. Studying organ metabolism may help to solve this problem. The objective of this study was to describe the tissue-specific metabolic fingerprints of fetal sheep under CPB and to associate them with organ functions. METHODS: Ten pregnant ewes at 90–120 days of gestation were randomly divided into two groups. The bypass group underwent a 1-h fetal CPB, whereas the control group underwent only a fetal sternotomy. During bypass, echocardiography, blood gases, and blood biochemistry were measured. After bypass, lambs were sacrificed, and tissues of the heart, liver, brain, kidney, and placenta were harvested. The metabolites extracted from these tissues were analyzed using non-targeted metabolomics based on liquid chromatography-mass spectrometry techniques. RESULTS: All tissues except the placenta displayed significant metabolic changes, and the fetal heart displayed obvious functional changes. Fetal sheep that underwent CPB had common and tissue-specific metabolic signatures. These changes can be attributed to dysregulated lipid metabolism, altered amino acid metabolism, and the accumulation of plasticizer metabolism. CONCLUSION: Fetal CPB causes tissue-specific metabolic changes in fetal sheep. Studying these metabolic changes, especially cardiac metabolism, is of great significance for the study of fetal CPB. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9791045/ /pubmed/36578834 http://dx.doi.org/10.3389/fcvm.2022.1009165 Text en Copyright © 2022 Wu, Teng, Tian, Huang, Deng, Li, Yuan, Chen, Li and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Wu, Wentao Teng, Yun Tian, Miao Huang, Bingxin Deng, Yuhang Li, Huili Yuan, Haiyun Chen, Jimei Li, Xiaohong Zhou, Chengbin Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
title | Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
title_full | Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
title_fullStr | Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
title_full_unstemmed | Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
title_short | Tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
title_sort | tissue-specific metabolomic profiling after cardiopulmonary bypass in fetal sheep |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791045/ https://www.ncbi.nlm.nih.gov/pubmed/36578834 http://dx.doi.org/10.3389/fcvm.2022.1009165 |
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