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The bile acid TUDCA reduces age-related hyperinsulinemia in mice

Aging is associated with glucose metabolism disturbances, such as insulin resistance and hyperinsulinemia, which contribute to the increased prevalence of type 2 diabetes (T2D) and its complications in the elderly population. In this sense, some bile acids have emerged as new therapeutic targets to...

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Autores principales: Zangerolamo, Lucas, Carvalho, Marina, Barssotti, Leticia, Soares, Gabriela M., Marmentini, Carine, Boschero, Antonio C., Barbosa, Helena Cristina L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789133/
https://www.ncbi.nlm.nih.gov/pubmed/36564463
http://dx.doi.org/10.1038/s41598-022-26915-3
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author Zangerolamo, Lucas
Carvalho, Marina
Barssotti, Leticia
Soares, Gabriela M.
Marmentini, Carine
Boschero, Antonio C.
Barbosa, Helena Cristina L.
author_facet Zangerolamo, Lucas
Carvalho, Marina
Barssotti, Leticia
Soares, Gabriela M.
Marmentini, Carine
Boschero, Antonio C.
Barbosa, Helena Cristina L.
author_sort Zangerolamo, Lucas
collection PubMed
description Aging is associated with glucose metabolism disturbances, such as insulin resistance and hyperinsulinemia, which contribute to the increased prevalence of type 2 diabetes (T2D) and its complications in the elderly population. In this sense, some bile acids have emerged as new therapeutic targets to treat TD2, as well as associated metabolic disorders. The taurine conjugated bile acid, tauroursodeoxycholic acid (TUDCA) improves glucose homeostasis in T2D, obesity, and Alzheimer's disease mice model. However, its effects in aged mice have not been explored yet. Here, we evaluated the actions of TUDCA upon glucose-insulin homeostasis in aged C57BL/6 male mice (18-month-old) treated with 300 mg/kg of TUDCA or its vehicle. TUDCA attenuated hyperinsulinemia and improved glucose homeostasis in aged mice, by enhancing liver insulin-degrading enzyme (IDE) expression and insulin clearance. Furthermore, the improvement in glucose-insulin homeostasis in these mice was accompanied by a reduction in adiposity, associated with adipocyte hypertrophy, and lipids accumulation in the liver. TUDCA-treated aged mice also displayed increased energy expenditure and metabolic flexibility, as well as a better cognitive ability. Taken together, our data highlight TUDCA as an interesting target for the attenuation of age-related hyperinsulinemia and its deleterious effects on metabolism.
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spelling pubmed-97891332022-12-25 The bile acid TUDCA reduces age-related hyperinsulinemia in mice Zangerolamo, Lucas Carvalho, Marina Barssotti, Leticia Soares, Gabriela M. Marmentini, Carine Boschero, Antonio C. Barbosa, Helena Cristina L. Sci Rep Article Aging is associated with glucose metabolism disturbances, such as insulin resistance and hyperinsulinemia, which contribute to the increased prevalence of type 2 diabetes (T2D) and its complications in the elderly population. In this sense, some bile acids have emerged as new therapeutic targets to treat TD2, as well as associated metabolic disorders. The taurine conjugated bile acid, tauroursodeoxycholic acid (TUDCA) improves glucose homeostasis in T2D, obesity, and Alzheimer's disease mice model. However, its effects in aged mice have not been explored yet. Here, we evaluated the actions of TUDCA upon glucose-insulin homeostasis in aged C57BL/6 male mice (18-month-old) treated with 300 mg/kg of TUDCA or its vehicle. TUDCA attenuated hyperinsulinemia and improved glucose homeostasis in aged mice, by enhancing liver insulin-degrading enzyme (IDE) expression and insulin clearance. Furthermore, the improvement in glucose-insulin homeostasis in these mice was accompanied by a reduction in adiposity, associated with adipocyte hypertrophy, and lipids accumulation in the liver. TUDCA-treated aged mice also displayed increased energy expenditure and metabolic flexibility, as well as a better cognitive ability. Taken together, our data highlight TUDCA as an interesting target for the attenuation of age-related hyperinsulinemia and its deleterious effects on metabolism. Nature Publishing Group UK 2022-12-23 /pmc/articles/PMC9789133/ /pubmed/36564463 http://dx.doi.org/10.1038/s41598-022-26915-3 Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zangerolamo, Lucas
Carvalho, Marina
Barssotti, Leticia
Soares, Gabriela M.
Marmentini, Carine
Boschero, Antonio C.
Barbosa, Helena Cristina L.
The bile acid TUDCA reduces age-related hyperinsulinemia in mice
title The bile acid TUDCA reduces age-related hyperinsulinemia in mice
title_full The bile acid TUDCA reduces age-related hyperinsulinemia in mice
title_fullStr The bile acid TUDCA reduces age-related hyperinsulinemia in mice
title_full_unstemmed The bile acid TUDCA reduces age-related hyperinsulinemia in mice
title_short The bile acid TUDCA reduces age-related hyperinsulinemia in mice
title_sort bile acid tudca reduces age-related hyperinsulinemia in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789133/
https://www.ncbi.nlm.nih.gov/pubmed/36564463
http://dx.doi.org/10.1038/s41598-022-26915-3
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