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Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring

Obesity during pregnancy increases the risk of cardiovascular problems, diabetes, asthma, and cognitive impairments, affecting the offspring. It is important to reduce the negative effects of obesity and high-fat (HF) diet during pregnancy. We employed a rat model of maternal HF diet to evaluate the...

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Autores principales: Tsai, Ti-An, Tsai, Chang-Ku, Huang, Li-Tung, Sheen, Jiunn-Ming, Tiao, Mao-Meng, Tain, You-Lin, Chen, Chih-Cheng, Lin, I-Chun, Lai, Yun-Ju, Tsai, Ching-Chou, Lin, Yu-Ju, Yu, Hong-Ren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215689/
https://www.ncbi.nlm.nih.gov/pubmed/32316577
http://dx.doi.org/10.3390/ijerph17082780
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author Tsai, Ti-An
Tsai, Chang-Ku
Huang, Li-Tung
Sheen, Jiunn-Ming
Tiao, Mao-Meng
Tain, You-Lin
Chen, Chih-Cheng
Lin, I-Chun
Lai, Yun-Ju
Tsai, Ching-Chou
Lin, Yu-Ju
Yu, Hong-Ren
author_facet Tsai, Ti-An
Tsai, Chang-Ku
Huang, Li-Tung
Sheen, Jiunn-Ming
Tiao, Mao-Meng
Tain, You-Lin
Chen, Chih-Cheng
Lin, I-Chun
Lai, Yun-Ju
Tsai, Ching-Chou
Lin, Yu-Ju
Yu, Hong-Ren
author_sort Tsai, Ti-An
collection PubMed
description Obesity during pregnancy increases the risk of cardiovascular problems, diabetes, asthma, and cognitive impairments, affecting the offspring. It is important to reduce the negative effects of obesity and high-fat (HF) diet during pregnancy. We employed a rat model of maternal HF diet to evaluate the possible de-programming effects of resveratrol in rodent male offspring with maternal HF diet/obesity. Male rat offspring were randomized into four groups: maternal control diet/postnatal control diet, maternal HF diet/postnatal control diet, maternal control diet plus maternal resveratrol treatment/postnatal control diet, and maternal HF diet plus maternal resveratrol treatment/postnatal control diet. Maternal HF diet during pregnancy plus lactation resulted in retroperitoneal adiposity in the male offspring. Maternal resveratrol treatment re-programmed maternal HF exposure-induced visceral adiposity. Offspring that received prenatal HF diet showed higher leptin/soluble leptin receptor (sOB-R) ratio than offspring that received prenatal control diet. Maternal resveratrol treatment ameliorated maternal HF exposure-induced increase in leptin/sOB-R ratio and altered the expression of genes for crucial fatty acid synthesis enzymes in the offspring. Thus, maternal resveratrol administration reduces retroperitoneal adiposity in rat offspring exposed to prenatal HF diet/obesity and could be used to ameliorate negative effects of maternal HF diet in the offspring.
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spelling pubmed-72156892020-05-22 Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring Tsai, Ti-An Tsai, Chang-Ku Huang, Li-Tung Sheen, Jiunn-Ming Tiao, Mao-Meng Tain, You-Lin Chen, Chih-Cheng Lin, I-Chun Lai, Yun-Ju Tsai, Ching-Chou Lin, Yu-Ju Yu, Hong-Ren Int J Environ Res Public Health Article Obesity during pregnancy increases the risk of cardiovascular problems, diabetes, asthma, and cognitive impairments, affecting the offspring. It is important to reduce the negative effects of obesity and high-fat (HF) diet during pregnancy. We employed a rat model of maternal HF diet to evaluate the possible de-programming effects of resveratrol in rodent male offspring with maternal HF diet/obesity. Male rat offspring were randomized into four groups: maternal control diet/postnatal control diet, maternal HF diet/postnatal control diet, maternal control diet plus maternal resveratrol treatment/postnatal control diet, and maternal HF diet plus maternal resveratrol treatment/postnatal control diet. Maternal HF diet during pregnancy plus lactation resulted in retroperitoneal adiposity in the male offspring. Maternal resveratrol treatment re-programmed maternal HF exposure-induced visceral adiposity. Offspring that received prenatal HF diet showed higher leptin/soluble leptin receptor (sOB-R) ratio than offspring that received prenatal control diet. Maternal resveratrol treatment ameliorated maternal HF exposure-induced increase in leptin/sOB-R ratio and altered the expression of genes for crucial fatty acid synthesis enzymes in the offspring. Thus, maternal resveratrol administration reduces retroperitoneal adiposity in rat offspring exposed to prenatal HF diet/obesity and could be used to ameliorate negative effects of maternal HF diet in the offspring. MDPI 2020-04-17 2020-04 /pmc/articles/PMC7215689/ /pubmed/32316577 http://dx.doi.org/10.3390/ijerph17082780 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tsai, Ti-An
Tsai, Chang-Ku
Huang, Li-Tung
Sheen, Jiunn-Ming
Tiao, Mao-Meng
Tain, You-Lin
Chen, Chih-Cheng
Lin, I-Chun
Lai, Yun-Ju
Tsai, Ching-Chou
Lin, Yu-Ju
Yu, Hong-Ren
Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring
title Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring
title_full Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring
title_fullStr Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring
title_full_unstemmed Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring
title_short Maternal Resveratrol Treatment Re-Programs and Maternal High-Fat Diet-Induced Retroperitoneal Adiposity in Male Offspring
title_sort maternal resveratrol treatment re-programs and maternal high-fat diet-induced retroperitoneal adiposity in male offspring
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215689/
https://www.ncbi.nlm.nih.gov/pubmed/32316577
http://dx.doi.org/10.3390/ijerph17082780
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