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Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice

An impaired decline in blood pressure at rest is typical in people with diabetes, reflects endothelial dysfunction, and increases the risk of end-organ damage. Here we report that microRNA-204 (miR-204) promotes endothelial dysfunction and impairment in blood pressure decline during inactivity. We s...

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Autores principales: Gaddam, Ravinder Reddy, Jacobsen, Veronica Peotta, Kim, Young-Rae, Gabani, Mohanad, Jacobs, Julia S., Dhuri, Karishma, Kumar, Santosh, Kassan, Modar, Li, Qiuxia, Bahal, Raman, Roghair, Robert, Irani, Kaikobad, Vikram, Ajit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308358/
https://www.ncbi.nlm.nih.gov/pubmed/32572127
http://dx.doi.org/10.1038/s41598-020-66786-0
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author Gaddam, Ravinder Reddy
Jacobsen, Veronica Peotta
Kim, Young-Rae
Gabani, Mohanad
Jacobs, Julia S.
Dhuri, Karishma
Kumar, Santosh
Kassan, Modar
Li, Qiuxia
Bahal, Raman
Roghair, Robert
Irani, Kaikobad
Vikram, Ajit
author_facet Gaddam, Ravinder Reddy
Jacobsen, Veronica Peotta
Kim, Young-Rae
Gabani, Mohanad
Jacobs, Julia S.
Dhuri, Karishma
Kumar, Santosh
Kassan, Modar
Li, Qiuxia
Bahal, Raman
Roghair, Robert
Irani, Kaikobad
Vikram, Ajit
author_sort Gaddam, Ravinder Reddy
collection PubMed
description An impaired decline in blood pressure at rest is typical in people with diabetes, reflects endothelial dysfunction, and increases the risk of end-organ damage. Here we report that microRNA-204 (miR-204) promotes endothelial dysfunction and impairment in blood pressure decline during inactivity. We show that db/db mice overexpress miR-204 in the aorta, and its absence rescues endothelial dysfunction and impaired blood pressure decline during inactivity despite obesity. The vascular miR-204 is sensitive to microbiota, and microbial suppression reversibly decreases aortic miR-204 and improves endothelial function, while the endothelial function of mice lacking miR-204 remained indifferent to the microbial alterations. We also show that the circulating miR-122 regulates vascular miR-204 as miR-122 inhibition decreases miR-204 in endothelial cells and aorta. This study establishes that miR-204 impairs endothelial function, promotes impairment in blood pressure decline during rest, and opens avenues for miR-204 inhibition strategies against vascular dysfunction.
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spelling pubmed-73083582020-06-23 Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice Gaddam, Ravinder Reddy Jacobsen, Veronica Peotta Kim, Young-Rae Gabani, Mohanad Jacobs, Julia S. Dhuri, Karishma Kumar, Santosh Kassan, Modar Li, Qiuxia Bahal, Raman Roghair, Robert Irani, Kaikobad Vikram, Ajit Sci Rep Article An impaired decline in blood pressure at rest is typical in people with diabetes, reflects endothelial dysfunction, and increases the risk of end-organ damage. Here we report that microRNA-204 (miR-204) promotes endothelial dysfunction and impairment in blood pressure decline during inactivity. We show that db/db mice overexpress miR-204 in the aorta, and its absence rescues endothelial dysfunction and impaired blood pressure decline during inactivity despite obesity. The vascular miR-204 is sensitive to microbiota, and microbial suppression reversibly decreases aortic miR-204 and improves endothelial function, while the endothelial function of mice lacking miR-204 remained indifferent to the microbial alterations. We also show that the circulating miR-122 regulates vascular miR-204 as miR-122 inhibition decreases miR-204 in endothelial cells and aorta. This study establishes that miR-204 impairs endothelial function, promotes impairment in blood pressure decline during rest, and opens avenues for miR-204 inhibition strategies against vascular dysfunction. Nature Publishing Group UK 2020-06-22 /pmc/articles/PMC7308358/ /pubmed/32572127 http://dx.doi.org/10.1038/s41598-020-66786-0 Text en © The Author(s) 2020 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
Gaddam, Ravinder Reddy
Jacobsen, Veronica Peotta
Kim, Young-Rae
Gabani, Mohanad
Jacobs, Julia S.
Dhuri, Karishma
Kumar, Santosh
Kassan, Modar
Li, Qiuxia
Bahal, Raman
Roghair, Robert
Irani, Kaikobad
Vikram, Ajit
Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
title Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
title_full Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
title_fullStr Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
title_full_unstemmed Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
title_short Microbiota-governed microRNA-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
title_sort microbiota-governed microrna-204 impairs endothelial function and blood pressure decline during inactivity in db/db mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308358/
https://www.ncbi.nlm.nih.gov/pubmed/32572127
http://dx.doi.org/10.1038/s41598-020-66786-0
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