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Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice
Bariatric surgeries such as the Vertical Sleeve Gastrectomy (VSG) are invasive but provide the most effective improvements in obesity and Type 2 diabetes. We hypothesized a potential role for the gut hormone Fibroblast-Growth Factor 15/19 which is increased after VSG and pharmacologically can improv...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346483/ https://www.ncbi.nlm.nih.gov/pubmed/34362888 http://dx.doi.org/10.1038/s41467-021-24914-y |
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author | Bozadjieva-Kramer, Nadejda Shin, Jae Hoon Shao, Yikai Gutierrez-Aguilar, Ruth Li, Ziru Heppner, Kristy M. Chiang, Samuel Vargo, Sara G. Granger, Katrina Sandoval, Darleen A. MacDougald, Ormond A. Seeley, Randy J. |
author_facet | Bozadjieva-Kramer, Nadejda Shin, Jae Hoon Shao, Yikai Gutierrez-Aguilar, Ruth Li, Ziru Heppner, Kristy M. Chiang, Samuel Vargo, Sara G. Granger, Katrina Sandoval, Darleen A. MacDougald, Ormond A. Seeley, Randy J. |
author_sort | Bozadjieva-Kramer, Nadejda |
collection | PubMed |
description | Bariatric surgeries such as the Vertical Sleeve Gastrectomy (VSG) are invasive but provide the most effective improvements in obesity and Type 2 diabetes. We hypothesized a potential role for the gut hormone Fibroblast-Growth Factor 15/19 which is increased after VSG and pharmacologically can improve energy homeostasis and glucose handling. We generated intestinal-specific FGF15 knockout (FGF15(INT-KO)) mice which were maintained on high-fat diet. FGF15(INT-KO) mice lost more weight after VSG as a result of increased lean tissue loss. FGF15(INT-KO) mice also lost more bone density and bone marrow adipose tissue after VSG. The effect of VSG to improve glucose tolerance was also absent in FGF15(INT-KO). VSG resulted in increased plasma bile acid levels but were considerably higher in VSG-FGF15(INT-KO) mice. These data point to an important role after VSG for intestinal FGF15 to protect the organism from deleterious effects of VSG potentially by limiting the increase in circulating bile acids. |
format | Online Article Text |
id | pubmed-8346483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83464832021-08-20 Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice Bozadjieva-Kramer, Nadejda Shin, Jae Hoon Shao, Yikai Gutierrez-Aguilar, Ruth Li, Ziru Heppner, Kristy M. Chiang, Samuel Vargo, Sara G. Granger, Katrina Sandoval, Darleen A. MacDougald, Ormond A. Seeley, Randy J. Nat Commun Article Bariatric surgeries such as the Vertical Sleeve Gastrectomy (VSG) are invasive but provide the most effective improvements in obesity and Type 2 diabetes. We hypothesized a potential role for the gut hormone Fibroblast-Growth Factor 15/19 which is increased after VSG and pharmacologically can improve energy homeostasis and glucose handling. We generated intestinal-specific FGF15 knockout (FGF15(INT-KO)) mice which were maintained on high-fat diet. FGF15(INT-KO) mice lost more weight after VSG as a result of increased lean tissue loss. FGF15(INT-KO) mice also lost more bone density and bone marrow adipose tissue after VSG. The effect of VSG to improve glucose tolerance was also absent in FGF15(INT-KO). VSG resulted in increased plasma bile acid levels but were considerably higher in VSG-FGF15(INT-KO) mice. These data point to an important role after VSG for intestinal FGF15 to protect the organism from deleterious effects of VSG potentially by limiting the increase in circulating bile acids. Nature Publishing Group UK 2021-08-06 /pmc/articles/PMC8346483/ /pubmed/34362888 http://dx.doi.org/10.1038/s41467-021-24914-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bozadjieva-Kramer, Nadejda Shin, Jae Hoon Shao, Yikai Gutierrez-Aguilar, Ruth Li, Ziru Heppner, Kristy M. Chiang, Samuel Vargo, Sara G. Granger, Katrina Sandoval, Darleen A. MacDougald, Ormond A. Seeley, Randy J. Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
title | Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
title_full | Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
title_fullStr | Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
title_full_unstemmed | Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
title_short | Intestinal-derived FGF15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
title_sort | intestinal-derived fgf15 protects against deleterious effects of vertical sleeve gastrectomy in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346483/ https://www.ncbi.nlm.nih.gov/pubmed/34362888 http://dx.doi.org/10.1038/s41467-021-24914-y |
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