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

dc.contributor.authorRobles-Vera, Iñaki
dc.contributor.authorde la Visitación, Néstor
dc.contributor.authorSánchez, Manuel
dc.contributor.authorGómez-Guzmán, Manuel
dc.contributor.authorJiménez, Rosario
dc.contributor.authorMoleón, Javier
dc.contributor.authorGonzález-Correa, Cristina
dc.contributor.authorRomero, Miguel
dc.contributor.authorYang, Tao
dc.contributor.authorRaizada, Mohan K
dc.contributor.authorToral, Marta
dc.contributor.authorDuarte, Juan
dc.date.accessioned2025-01-07T15:01:40Z
dc.date.available2025-01-07T15:01:40Z
dc.date.issued2020-11-28
dc.description.abstractMicrobiota 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.
dc.identifier.doi10.3390/antiox9121199
dc.identifier.issn2076-3921
dc.identifier.pmcPMC7761232
dc.identifier.pmid33260593
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC7761232/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2076-3921/9/12/1199/pdf
dc.identifier.urihttps://hdl.handle.net/10668/26809
dc.issue.number12
dc.journal.titleAntioxidants (Basel, Switzerland)
dc.journal.titleabbreviationAntioxidants (Basel)
dc.language.isoen
dc.organizationSAS - Hospital de La Axarquía
dc.organizationSAS - D.S.A.P. Málaga
dc.organizationInstituto de Investigación Biomédica de Málaga - Plataforma Bionand (IBIMA)
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject(deoxycorticosterone acetate) DOCA-salt model
dc.subjectgut dysbiosis
dc.subjecthypertension
dc.subjectinflammation
dc.subjectmycophenolate
dc.subjectoxidative stress
dc.titleMycophenolate Improves Brain-Gut Axis Inducing Remodeling of Gut Microbiota in DOCA-Salt Hypertensive Rats.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number9

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