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Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications
Maternal high-fat (HF) diet exposure in utero may affect fetal development and cause metabolic problems throughout life due to lipid dysmetabolism and oxidative damage. Metformin has been suggested as a potential treatment for body weight reduction and nonalcoholic fatty liver disease, but its repro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694630/ https://www.ncbi.nlm.nih.gov/pubmed/36430717 http://dx.doi.org/10.3390/ijms232214239 |
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author | Huang, Chien-Fu Tiao, Mao-Meng Lin, I-Chun Huang, Li-Tung Sheen, Jiunn-Ming Tain, You-Lin Hsu, Chien-Ning Tsai, Ching-Chou Lin, Yu-Ju Yu, Hong-Ren |
author_facet | Huang, Chien-Fu Tiao, Mao-Meng Lin, I-Chun Huang, Li-Tung Sheen, Jiunn-Ming Tain, You-Lin Hsu, Chien-Ning Tsai, Ching-Chou Lin, Yu-Ju Yu, Hong-Ren |
author_sort | Huang, Chien-Fu |
collection | PubMed |
description | Maternal high-fat (HF) diet exposure in utero may affect fetal development and cause metabolic problems throughout life due to lipid dysmetabolism and oxidative damage. Metformin has been suggested as a potential treatment for body weight reduction and nonalcoholic fatty liver disease, but its reprogramming effect on offspring is undetermined. This study assesses the effects of maternal metformin treatment on hepatic steatosis in offspring caused by maternal HF diet. Female rats were fed either a control or an HF diet before conception, with or without metformin treatment during gestation, and placenta and fetal liver tissues were collected. In another experiment, the offspring were fed a control diet until 120 d (adult stage). Metformin treatment during pregnancy ameliorates placental oxidative stress and enhances placental glucose transporter 1 (GLUT1), GLUT3, and GLUT4 expression levels through 5’ adenosine monophosphate-activated protein kinase (AMPK) activation. Maternal metformin treatment was shown to reprogram maternal HF diet-induced changes in offspring fatty liver with the effects observed in adulthood as well. Further validation is required to develop maternal metformin therapy for clinical applications. |
format | Online Article Text |
id | pubmed-9694630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96946302022-11-26 Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications Huang, Chien-Fu Tiao, Mao-Meng Lin, I-Chun Huang, Li-Tung Sheen, Jiunn-Ming Tain, You-Lin Hsu, Chien-Ning Tsai, Ching-Chou Lin, Yu-Ju Yu, Hong-Ren Int J Mol Sci Article Maternal high-fat (HF) diet exposure in utero may affect fetal development and cause metabolic problems throughout life due to lipid dysmetabolism and oxidative damage. Metformin has been suggested as a potential treatment for body weight reduction and nonalcoholic fatty liver disease, but its reprogramming effect on offspring is undetermined. This study assesses the effects of maternal metformin treatment on hepatic steatosis in offspring caused by maternal HF diet. Female rats were fed either a control or an HF diet before conception, with or without metformin treatment during gestation, and placenta and fetal liver tissues were collected. In another experiment, the offspring were fed a control diet until 120 d (adult stage). Metformin treatment during pregnancy ameliorates placental oxidative stress and enhances placental glucose transporter 1 (GLUT1), GLUT3, and GLUT4 expression levels through 5’ adenosine monophosphate-activated protein kinase (AMPK) activation. Maternal metformin treatment was shown to reprogram maternal HF diet-induced changes in offspring fatty liver with the effects observed in adulthood as well. Further validation is required to develop maternal metformin therapy for clinical applications. MDPI 2022-11-17 /pmc/articles/PMC9694630/ /pubmed/36430717 http://dx.doi.org/10.3390/ijms232214239 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Huang, Chien-Fu Tiao, Mao-Meng Lin, I-Chun Huang, Li-Tung Sheen, Jiunn-Ming Tain, You-Lin Hsu, Chien-Ning Tsai, Ching-Chou Lin, Yu-Ju Yu, Hong-Ren Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications |
title | Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications |
title_full | Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications |
title_fullStr | Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications |
title_full_unstemmed | Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications |
title_short | Maternal Metformin Treatment Reprograms Maternal High-Fat Diet-Induced Hepatic Steatosis in Offspring Associated with Placental Glucose Transporter Modifications |
title_sort | maternal metformin treatment reprograms maternal high-fat diet-induced hepatic steatosis in offspring associated with placental glucose transporter modifications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694630/ https://www.ncbi.nlm.nih.gov/pubmed/36430717 http://dx.doi.org/10.3390/ijms232214239 |
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