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Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats

Resveratrol butyrate esters (RBE) are derivatives of resveratrol (RSV) and butyric acid and exhibit biological activity similar to that of RSV but with higher bioavailability. The aim of this study was designed as an animal experiment to explore the effects of RBE on the serum biochemistry, and fat...

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Autores principales: Shih, Ming-Kuei, Tain, You-Lin, Chen, Yu-Wei, Hsu, Wei-Hsuan, Yeh, Yao-Tsung, Chang, Sam K. C., Liao, Jin-Xian, Hou, Chih-Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271435/
https://www.ncbi.nlm.nih.gov/pubmed/34209270
http://dx.doi.org/10.3390/molecules26134010
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author Shih, Ming-Kuei
Tain, You-Lin
Chen, Yu-Wei
Hsu, Wei-Hsuan
Yeh, Yao-Tsung
Chang, Sam K. C.
Liao, Jin-Xian
Hou, Chih-Yao
author_facet Shih, Ming-Kuei
Tain, You-Lin
Chen, Yu-Wei
Hsu, Wei-Hsuan
Yeh, Yao-Tsung
Chang, Sam K. C.
Liao, Jin-Xian
Hou, Chih-Yao
author_sort Shih, Ming-Kuei
collection PubMed
description Resveratrol butyrate esters (RBE) are derivatives of resveratrol (RSV) and butyric acid and exhibit biological activity similar to that of RSV but with higher bioavailability. The aim of this study was designed as an animal experiment to explore the effects of RBE on the serum biochemistry, and fat deposits in the offspring rats exposed to bisphenol A (BPA), along with the growth and decline of gut microbiota. We constructed an animal model of perinatal Bisphenol A (BPA) exposure to observe the effects of RBE supplementation on obesity, blood lipids, and intestinal microbiota in female offspring rats. Perinatal exposure to BPA led to weight gain, lipid accumulation, high levels of blood lipids, and deterioration of intestinal microbiota in female offspring rats. RBE supplementation reduced the weight gain and lipid accumulation caused by BPA, optimised the levels of blood lipids, significantly reduced the Firmicutes/Bacteroidetes (F/B) ratio, and increased and decreased the abundance of S24-7 and Lactobacillus, respectively. The analysis of faecal short-chain fatty acid (SCFA) levels revealed that BPA exposure increased the faecal concentration of acetate, which could be reduced via RBE supplementation. However, the faecal concentrations of propionate and butyrate were not only significantly lower than that of acetate, but also did not significantly change in response to BPA exposure or RBE supplementation. Hence, RBE can suppress BPA-induced obesity in female offspring rats, and it demonstrates excellent modulatory activity on intestinal microbiota, with potential applications in perinatological research.
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spelling pubmed-82714352021-07-11 Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats Shih, Ming-Kuei Tain, You-Lin Chen, Yu-Wei Hsu, Wei-Hsuan Yeh, Yao-Tsung Chang, Sam K. C. Liao, Jin-Xian Hou, Chih-Yao Molecules Article Resveratrol butyrate esters (RBE) are derivatives of resveratrol (RSV) and butyric acid and exhibit biological activity similar to that of RSV but with higher bioavailability. The aim of this study was designed as an animal experiment to explore the effects of RBE on the serum biochemistry, and fat deposits in the offspring rats exposed to bisphenol A (BPA), along with the growth and decline of gut microbiota. We constructed an animal model of perinatal Bisphenol A (BPA) exposure to observe the effects of RBE supplementation on obesity, blood lipids, and intestinal microbiota in female offspring rats. Perinatal exposure to BPA led to weight gain, lipid accumulation, high levels of blood lipids, and deterioration of intestinal microbiota in female offspring rats. RBE supplementation reduced the weight gain and lipid accumulation caused by BPA, optimised the levels of blood lipids, significantly reduced the Firmicutes/Bacteroidetes (F/B) ratio, and increased and decreased the abundance of S24-7 and Lactobacillus, respectively. The analysis of faecal short-chain fatty acid (SCFA) levels revealed that BPA exposure increased the faecal concentration of acetate, which could be reduced via RBE supplementation. However, the faecal concentrations of propionate and butyrate were not only significantly lower than that of acetate, but also did not significantly change in response to BPA exposure or RBE supplementation. Hence, RBE can suppress BPA-induced obesity in female offspring rats, and it demonstrates excellent modulatory activity on intestinal microbiota, with potential applications in perinatological research. MDPI 2021-06-30 /pmc/articles/PMC8271435/ /pubmed/34209270 http://dx.doi.org/10.3390/molecules26134010 Text en © 2021 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
Shih, Ming-Kuei
Tain, You-Lin
Chen, Yu-Wei
Hsu, Wei-Hsuan
Yeh, Yao-Tsung
Chang, Sam K. C.
Liao, Jin-Xian
Hou, Chih-Yao
Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats
title Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats
title_full Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats
title_fullStr Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats
title_full_unstemmed Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats
title_short Resveratrol Butyrate Esters Inhibit Obesity Caused by Perinatal Exposure to Bisphenol A in Female Offspring Rats
title_sort resveratrol butyrate esters inhibit obesity caused by perinatal exposure to bisphenol a in female offspring rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271435/
https://www.ncbi.nlm.nih.gov/pubmed/34209270
http://dx.doi.org/10.3390/molecules26134010
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