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Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis

A maternal high-fat diet (HFD) can impact the offspring’s development of liver steatosis, with fetal development in utero being a crucial period. Therefore, this study investigated the mechanism and whether butyrate can rescue liver injury caused by maternal HFD in the fetus. Pregnant female Sprague...

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Autores principales: Huang, Yu-Jyun, Wang, Pei-Ming, Tang, Kuo-Shu, Chen, Chih-Jen, Huang, Ying-Hsien, Tiao, Mao-Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258878/
https://www.ncbi.nlm.nih.gov/pubmed/35793323
http://dx.doi.org/10.1371/journal.pone.0270657
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author Huang, Yu-Jyun
Wang, Pei-Ming
Tang, Kuo-Shu
Chen, Chih-Jen
Huang, Ying-Hsien
Tiao, Mao-Meng
author_facet Huang, Yu-Jyun
Wang, Pei-Ming
Tang, Kuo-Shu
Chen, Chih-Jen
Huang, Ying-Hsien
Tiao, Mao-Meng
author_sort Huang, Yu-Jyun
collection PubMed
description A maternal high-fat diet (HFD) can impact the offspring’s development of liver steatosis, with fetal development in utero being a crucial period. Therefore, this study investigated the mechanism and whether butyrate can rescue liver injury caused by maternal HFD in the fetus. Pregnant female Sprague Dawley rats were randomly divided into two groups, prenatal HFD (58% fat) exposure or normal control diet (4.5% fat). The HFD group was fed an HFD 7 weeks before mating and during gestation until sacrifice at gestation 21 days. After confirmation of mating, the other HFD group was supplemented with sodium butyrate (HFSB). The results showed that maternal liver histology showed lipid accumulation with steatosis and shortened ileum villi in HFD, which was ameliorated in the HFSB group (P<0.05). There was increased fetal liver and ileum TUNEL staining and IL-6 expression with increased fetal liver TNF-α and malondialdehyde expression in the HFD group (P<0.05), which decreased in the HFSB group (P<0.05). The fetal liver expression of phospho-AKT/AKT and GPX1 decreased in the HFD group but increased in the HFSB group (P<0.05). In conclusion that oxidative stress with inflammation and apoptosis plays a vital role after maternal HFD in the fetus liver that can be ameliorated with butyrate supplementation.
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spelling pubmed-92588782022-07-07 Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis Huang, Yu-Jyun Wang, Pei-Ming Tang, Kuo-Shu Chen, Chih-Jen Huang, Ying-Hsien Tiao, Mao-Meng PLoS One Research Article A maternal high-fat diet (HFD) can impact the offspring’s development of liver steatosis, with fetal development in utero being a crucial period. Therefore, this study investigated the mechanism and whether butyrate can rescue liver injury caused by maternal HFD in the fetus. Pregnant female Sprague Dawley rats were randomly divided into two groups, prenatal HFD (58% fat) exposure or normal control diet (4.5% fat). The HFD group was fed an HFD 7 weeks before mating and during gestation until sacrifice at gestation 21 days. After confirmation of mating, the other HFD group was supplemented with sodium butyrate (HFSB). The results showed that maternal liver histology showed lipid accumulation with steatosis and shortened ileum villi in HFD, which was ameliorated in the HFSB group (P<0.05). There was increased fetal liver and ileum TUNEL staining and IL-6 expression with increased fetal liver TNF-α and malondialdehyde expression in the HFD group (P<0.05), which decreased in the HFSB group (P<0.05). The fetal liver expression of phospho-AKT/AKT and GPX1 decreased in the HFD group but increased in the HFSB group (P<0.05). In conclusion that oxidative stress with inflammation and apoptosis plays a vital role after maternal HFD in the fetus liver that can be ameliorated with butyrate supplementation. Public Library of Science 2022-07-06 /pmc/articles/PMC9258878/ /pubmed/35793323 http://dx.doi.org/10.1371/journal.pone.0270657 Text en © 2022 Huang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Huang, Yu-Jyun
Wang, Pei-Ming
Tang, Kuo-Shu
Chen, Chih-Jen
Huang, Ying-Hsien
Tiao, Mao-Meng
Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
title Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
title_full Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
title_fullStr Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
title_full_unstemmed Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
title_short Butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
title_sort butyrate ameliorates maternal high-fat diet-induced fetal liver cellular apoptosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258878/
https://www.ncbi.nlm.nih.gov/pubmed/35793323
http://dx.doi.org/10.1371/journal.pone.0270657
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