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Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice
Estrogens protect against diet-induced obesity in women and female rodents. For example, a lack of estrogens in postmenopausal women is associated with an increased risk of weight gain, cardiovascular diseases, low-grade inflammation, and cancer. Estrogens act with leptin to regulate energy homeosta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934844/ https://www.ncbi.nlm.nih.gov/pubmed/31882890 http://dx.doi.org/10.1038/s41598-019-56723-1 |
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author | Acharya, Kalpana D. Gao, Xing Bless, Elizabeth P. Chen, Jun Tetel, Marc J. |
author_facet | Acharya, Kalpana D. Gao, Xing Bless, Elizabeth P. Chen, Jun Tetel, Marc J. |
author_sort | Acharya, Kalpana D. |
collection | PubMed |
description | Estrogens protect against diet-induced obesity in women and female rodents. For example, a lack of estrogens in postmenopausal women is associated with an increased risk of weight gain, cardiovascular diseases, low-grade inflammation, and cancer. Estrogens act with leptin to regulate energy homeostasis in females. Leptin-deficient mice (ob/ob) exhibit morbid obesity and insulin resistance. The gut microbiome is also critical in regulating metabolism. The present study investigates whether estrogens and leptin modulate gut microbiota in ovariectomized ob/ob (obese) or heterozygote (lean) mice fed high-fat diet (HFD) that received either 17β-Estradiol (E2) or vehicle implants. E2 attenuated weight gain in both genotypes. Moreover, both obesity (ob/ob mice) and E2 were associated with reduced gut microbial diversity. ob/ob mice exhibited lower species richness than control mice, while E2-treated mice had reduced evenness compared with vehicle mice. Regarding taxa, E2 was associated with an increased abundance of the S24-7 family, while leptin was associated with increases in Coriobacteriaceae, Clostridium and Lactobacillus. Some taxa were affected by both E2 and leptin, suggesting these hormones alter gut microbiota of HFD-fed female mice. Understanding the role of E2 and leptin in regulating gut microbiota will provide important insights into hormone-dependent metabolic disorders in women. |
format | Online Article Text |
id | pubmed-6934844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69348442019-12-31 Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice Acharya, Kalpana D. Gao, Xing Bless, Elizabeth P. Chen, Jun Tetel, Marc J. Sci Rep Article Estrogens protect against diet-induced obesity in women and female rodents. For example, a lack of estrogens in postmenopausal women is associated with an increased risk of weight gain, cardiovascular diseases, low-grade inflammation, and cancer. Estrogens act with leptin to regulate energy homeostasis in females. Leptin-deficient mice (ob/ob) exhibit morbid obesity and insulin resistance. The gut microbiome is also critical in regulating metabolism. The present study investigates whether estrogens and leptin modulate gut microbiota in ovariectomized ob/ob (obese) or heterozygote (lean) mice fed high-fat diet (HFD) that received either 17β-Estradiol (E2) or vehicle implants. E2 attenuated weight gain in both genotypes. Moreover, both obesity (ob/ob mice) and E2 were associated with reduced gut microbial diversity. ob/ob mice exhibited lower species richness than control mice, while E2-treated mice had reduced evenness compared with vehicle mice. Regarding taxa, E2 was associated with an increased abundance of the S24-7 family, while leptin was associated with increases in Coriobacteriaceae, Clostridium and Lactobacillus. Some taxa were affected by both E2 and leptin, suggesting these hormones alter gut microbiota of HFD-fed female mice. Understanding the role of E2 and leptin in regulating gut microbiota will provide important insights into hormone-dependent metabolic disorders in women. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934844/ /pubmed/31882890 http://dx.doi.org/10.1038/s41598-019-56723-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Acharya, Kalpana D. Gao, Xing Bless, Elizabeth P. Chen, Jun Tetel, Marc J. Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
title | Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
title_full | Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
title_fullStr | Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
title_full_unstemmed | Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
title_short | Estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
title_sort | estradiol and high fat diet associate with changes in gut microbiota in female ob/ob mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934844/ https://www.ncbi.nlm.nih.gov/pubmed/31882890 http://dx.doi.org/10.1038/s41598-019-56723-1 |
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