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Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet
Obesity is a major driver of metabolic diseases such as nonalcoholic fatty liver disease, certain cancers, and insulin resistance. However, there are no effective drugs to treat obesity. Betaine is a nontoxic, chemically stable and naturally occurring molecule. This study shows that dietary betaine...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852707/ https://www.ncbi.nlm.nih.gov/pubmed/29373534 http://dx.doi.org/10.3390/nu10020131 |
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author | Du, Jingjing Shen, Linyuan Tan, Zhendong Zhang, Peiwen Zhao, Xue Xu, Yan Gan, Mailing Yang, Qiong Ma, Jideng Jiang, An’an Tang, Guoqing Jiang, Yanzhi Jin, Long Li, Mingzhou Bai, Lin Li, Xuewei Wang, Jinyong Zhang, Shunhua Zhu, Li |
author_facet | Du, Jingjing Shen, Linyuan Tan, Zhendong Zhang, Peiwen Zhao, Xue Xu, Yan Gan, Mailing Yang, Qiong Ma, Jideng Jiang, An’an Tang, Guoqing Jiang, Yanzhi Jin, Long Li, Mingzhou Bai, Lin Li, Xuewei Wang, Jinyong Zhang, Shunhua Zhu, Li |
author_sort | Du, Jingjing |
collection | PubMed |
description | Obesity is a major driver of metabolic diseases such as nonalcoholic fatty liver disease, certain cancers, and insulin resistance. However, there are no effective drugs to treat obesity. Betaine is a nontoxic, chemically stable and naturally occurring molecule. This study shows that dietary betaine supplementation significantly inhibits the white fat production in a high-fat diet (HFD)-induced obese mice. This might be due to betaine preventing the formation of new white fat (WAT), and guiding the original WAT to burn through stimulated mitochondrial biogenesis and promoting browning of WAT. Furthermore, dietary betaine supplementation decreases intramyocellular lipid accumulation in HFD-induced obese mice. Further analysis shows that betaine supplementation reduced intramyocellular lipid accumulation might be associated with increasing polyunsaturated fatty acids (PUFA), fatty acid oxidation, and the inhibition of fatty acid synthesis in muscle. Notably, by performing insulin-tolerance tests (ITTs) and glucose-tolerance tests (GTTs), dietary betaine supplementation could be observed for improvement of obesity and non-obesity induced insulin resistance. Together, these findings could suggest that inhibiting WAT production, intramyocellular lipid accumulation and inflammation, betaine supplementation limits HFD-induced obesity and improves insulin resistance. |
format | Online Article Text |
id | pubmed-5852707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58527072018-03-19 Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet Du, Jingjing Shen, Linyuan Tan, Zhendong Zhang, Peiwen Zhao, Xue Xu, Yan Gan, Mailing Yang, Qiong Ma, Jideng Jiang, An’an Tang, Guoqing Jiang, Yanzhi Jin, Long Li, Mingzhou Bai, Lin Li, Xuewei Wang, Jinyong Zhang, Shunhua Zhu, Li Nutrients Article Obesity is a major driver of metabolic diseases such as nonalcoholic fatty liver disease, certain cancers, and insulin resistance. However, there are no effective drugs to treat obesity. Betaine is a nontoxic, chemically stable and naturally occurring molecule. This study shows that dietary betaine supplementation significantly inhibits the white fat production in a high-fat diet (HFD)-induced obese mice. This might be due to betaine preventing the formation of new white fat (WAT), and guiding the original WAT to burn through stimulated mitochondrial biogenesis and promoting browning of WAT. Furthermore, dietary betaine supplementation decreases intramyocellular lipid accumulation in HFD-induced obese mice. Further analysis shows that betaine supplementation reduced intramyocellular lipid accumulation might be associated with increasing polyunsaturated fatty acids (PUFA), fatty acid oxidation, and the inhibition of fatty acid synthesis in muscle. Notably, by performing insulin-tolerance tests (ITTs) and glucose-tolerance tests (GTTs), dietary betaine supplementation could be observed for improvement of obesity and non-obesity induced insulin resistance. Together, these findings could suggest that inhibiting WAT production, intramyocellular lipid accumulation and inflammation, betaine supplementation limits HFD-induced obesity and improves insulin resistance. MDPI 2018-01-26 /pmc/articles/PMC5852707/ /pubmed/29373534 http://dx.doi.org/10.3390/nu10020131 Text en © 2018 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 Du, Jingjing Shen, Linyuan Tan, Zhendong Zhang, Peiwen Zhao, Xue Xu, Yan Gan, Mailing Yang, Qiong Ma, Jideng Jiang, An’an Tang, Guoqing Jiang, Yanzhi Jin, Long Li, Mingzhou Bai, Lin Li, Xuewei Wang, Jinyong Zhang, Shunhua Zhu, Li Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet |
title | Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet |
title_full | Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet |
title_fullStr | Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet |
title_full_unstemmed | Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet |
title_short | Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet |
title_sort | betaine supplementation enhances lipid metabolism and improves insulin resistance in mice fed a high-fat diet |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852707/ https://www.ncbi.nlm.nih.gov/pubmed/29373534 http://dx.doi.org/10.3390/nu10020131 |
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