Use el DOI o este identificador para enlazar este recurso: http://ru.facmed.unam.mx/jspui/handle/FACMED_UNAM/A101
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dc.contributor.authorAlejandra Romo Araiza
dc.contributor.authorGutierrez Salmean, Gabriela
dc.contributor.authorGonzalez Galvan, Emilio Jorge
dc.contributor.authorHernandez Frausto, Melissa Guadalupe
dc.contributor.authorHerrera Lopez, Gabriel
dc.contributor.authorRomo Parra, Hector Manuel
dc.contributor.authorGarcia Contreras, Rodolfo
dc.contributor.authorFernandez Presas, Ana Maria
dc.contributor.authorJasso Chavez, Ricardo
dc.contributor.authorCesar Borlongan
dc.coverage.spatialCH
dc.date.accessioned2019-06-17T17:23:06Z-
dc.date.available2019-06-17T17:23:06Z-
dc.date.issued2018
dc.identifier.urihttp://ru.facmed.unam.mx/jspui/handle/FACMED_UNAM/A101-
dc.description.abstractAging is associated with morphological, physiological and metabolic changes, leading to multiorgan degenerative pathologies, such as cognitive function decline. It has been suggested that memory loss also involves a decrease in neurotrophic factors, including brain-derived neurotrophic factor (BDNF). In recent years, microbiota has been proposed as an essential player in brain development, as it is believed to activate BDNF secretion through butyrate production. Thus, microbiota modulation by supplementation with probiotics and prebiotics may impact cognitive decline. This study aimed to evaluate the effects of probiotics and prebiotics supplementation on the memory of middle-aged rats. Sprague-Dawley male rats were randomized in four groups (n = 13 per group): control (water), probiotic (E. faecium), prebiotic (agave inulin), symbiotic (E. faecium + inulin), which were administered for 5 weeks by oral gavage. Spatial and associative memory was analyzed using the Morris Water Maze (MWM) and Pavlovian autoshaping tests, respectively. Hippocampus was obtained to analyze cytokines [interleukin (IL-1?) and tumor necrosis factor (TNF-?)], BDNF and ?-aminobutyric acid (GABA) by enzyme-linked immunosorbent assay (ELISA). Butyrate concentrations were also evaluated in feces. The symbiotic group showed a significantly better performance in MWM (p < 0.01), but not in Pavlovian autoshaping test. It also showed significantly lower concentrations of pro-inflammatory cytokines (p < 0.01) and the reduction in IL-1? correlated with a better performance of the symbiotic group in MWM (p < 0.05). Symbiotic group also showed the highest BDNF and butyrate levels (p < 0.0001). Finally, we compared the electrophysiological response of control (n = 8) and symbiotic (n = 8) groups. Passive properties of CA1 pyramidal cells (PCs) exhibited changes in response to the symbiotic treatment. Likewise, this group showed an increase in the N-methyl-D-aspartate receptor (NMDA)/AMPA ratio and exhibited robust long-term potentiation (LTP; p < 0.01). Integrated results suggest that symbiotics could improve age-related impaired memory.
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.rightsopenAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0
dc.subjectMemoria asociativa
dc.subjectButirato
dc.subjectMemoria espacial
dc.subjectProbióticos
dc.subjectPrebióticos
dc.subject.classificationMedicina y Ciencias de la Salud
dc.subject.otherAssociative memory
dc.subject.otherButyrate
dc.subject.otherSpatial memory
dc.subject.otherProbiotics
dc.subject.otherPrebiotics
dc.titleProbiotics and Prebiotics as a Therapeutic Strategy to Improve Memory in a Model of Middle-Aged Rats.
dc.typeArtículo
dc.typepublishedVersion
dcterms.bibliographicCitationFrontiers in Aging Neuroscience (1663-4365) vol. 10 (1), 1-15 (2018)
dcterms.creatorAlejandra Romo Araiza::orcid::0000-0003-4950-910X
dcterms.creatorGutierrez Salmean, Gabriela::cvu::282767
dcterms.creatorGonzalez Galvan, Emilio Jorge::cvu::19100
dcterms.creatorHernandez Frausto, Melissa Guadalupe::cvu::487459
dcterms.creatorHerrera Lopez, Gabriel::cvu::558271
dcterms.creatorRomo Parra, Hector Manuel::cvu::37574
dcterms.creatorGarcia Contreras, Rodolfo::cvu::40169
dcterms.creatorFernandez Presas, Ana Maria::cvu::120695
dcterms.creatorJasso Chavez, Ricardo::cvu::25535
dcterms.creatorCesar Borlongan::orcid::0000-0002-2966-9782
dc.identifier.doi10.3389/fnagi.2018.00416
dc.relation.ispartofjournalhttps://www.ncbi.nlm.nih.gov/pmc/issues/305355/
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