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Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats

Microbiota is involved in the host blood pressure (BP) regulation. The immunosuppressive drug mofetil mycophenolate (MMF) ameliorates hypertension. The present study analyzed whether MMF improves dysbiosis in mineralocorticoid-induced hypertension. Male Wistar rats were assigned to three groups: unt...

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Autores principales: Robles-Vera, Iñaki, de la Visitación, Néstor, Sánchez, Manuel, Gómez-Guzmán, Manuel, Jiménez, Rosario, Moleón, Javier, González-Correa, Cristina, Romero, Miguel, Yang, Tao, Raizada, Mohan K., Toral, Marta, Duarte, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7761232/
https://www.ncbi.nlm.nih.gov/pubmed/33260593
http://dx.doi.org/10.3390/antiox9121199
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author Robles-Vera, Iñaki
de la Visitación, Néstor
Sánchez, Manuel
Gómez-Guzmán, Manuel
Jiménez, Rosario
Moleón, Javier
González-Correa, Cristina
Romero, Miguel
Yang, Tao
Raizada, Mohan K.
Toral, Marta
Duarte, Juan
author_facet Robles-Vera, Iñaki
de la Visitación, Néstor
Sánchez, Manuel
Gómez-Guzmán, Manuel
Jiménez, Rosario
Moleón, Javier
González-Correa, Cristina
Romero, Miguel
Yang, Tao
Raizada, Mohan K.
Toral, Marta
Duarte, Juan
author_sort Robles-Vera, Iñaki
collection PubMed
description Microbiota is involved in the host blood pressure (BP) regulation. The immunosuppressive drug mofetil mycophenolate (MMF) ameliorates hypertension. The present study analyzed whether MMF improves dysbiosis in mineralocorticoid-induced hypertension. Male Wistar rats were assigned to three groups: untreated (CTR), deoxycorticosterone acetate (DOCA)-salt, and DOCA treated with MMF for 4 weeks. MMF treatment reduced systolic BP, improved endothelial dysfunction, and reduced oxidative stress and inflammation in aorta. A clear separation in the gut bacterial community between CTR and DOCA groups was found, whereas the cluster belonging to DOCA-MMF group was found to be intermixed. No changes were found at the phylum level among all experimental groups. MMF restored the elevation in lactate-producing bacteria found in DOCA-salt joined to an increase in the acetate-producing bacteria. MMF restored the percentage of anaerobic bacteria in the DOCA-salt group to values similar to control rats. The improvement of gut dysbiosis was associated with an enhanced colonic integrity and a decreased sympathetic drive in the gut. MMF inhibited neuroinflammation in the paraventricular nuclei in the hypothalamus. This study demonstrates for the first time that MMF reduces gut dysbiosis in DOCA-salt hypertension models. This effect seems to be related to its capacity to improve gut integrity due to reduced sympathetic drive in the gut associated with reduced brain neuroinflammation.
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spelling pubmed-77612322020-12-26 Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats Robles-Vera, Iñaki de la Visitación, Néstor Sánchez, Manuel Gómez-Guzmán, Manuel Jiménez, Rosario Moleón, Javier González-Correa, Cristina Romero, Miguel Yang, Tao Raizada, Mohan K. Toral, Marta Duarte, Juan Antioxidants (Basel) Article Microbiota is involved in the host blood pressure (BP) regulation. The immunosuppressive drug mofetil mycophenolate (MMF) ameliorates hypertension. The present study analyzed whether MMF improves dysbiosis in mineralocorticoid-induced hypertension. Male Wistar rats were assigned to three groups: untreated (CTR), deoxycorticosterone acetate (DOCA)-salt, and DOCA treated with MMF for 4 weeks. MMF treatment reduced systolic BP, improved endothelial dysfunction, and reduced oxidative stress and inflammation in aorta. A clear separation in the gut bacterial community between CTR and DOCA groups was found, whereas the cluster belonging to DOCA-MMF group was found to be intermixed. No changes were found at the phylum level among all experimental groups. MMF restored the elevation in lactate-producing bacteria found in DOCA-salt joined to an increase in the acetate-producing bacteria. MMF restored the percentage of anaerobic bacteria in the DOCA-salt group to values similar to control rats. The improvement of gut dysbiosis was associated with an enhanced colonic integrity and a decreased sympathetic drive in the gut. MMF inhibited neuroinflammation in the paraventricular nuclei in the hypothalamus. This study demonstrates for the first time that MMF reduces gut dysbiosis in DOCA-salt hypertension models. This effect seems to be related to its capacity to improve gut integrity due to reduced sympathetic drive in the gut associated with reduced brain neuroinflammation. MDPI 2020-11-28 /pmc/articles/PMC7761232/ /pubmed/33260593 http://dx.doi.org/10.3390/antiox9121199 Text en © 2020 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
Robles-Vera, Iñaki
de la Visitación, Néstor
Sánchez, Manuel
Gómez-Guzmán, Manuel
Jiménez, Rosario
Moleón, Javier
González-Correa, Cristina
Romero, Miguel
Yang, Tao
Raizada, Mohan K.
Toral, Marta
Duarte, Juan
Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats
title Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats
title_full Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats
title_fullStr Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats
title_full_unstemmed Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats
title_short Mycophenolate Improves Brain–Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats
title_sort mycophenolate improves brain–gut axis inducing remodeling of gut microbiota in doca-salt hypertensive rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7761232/
https://www.ncbi.nlm.nih.gov/pubmed/33260593
http://dx.doi.org/10.3390/antiox9121199
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