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dc.contributor.author
Sato, Amy Y.  
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Cregor, Meloney  
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Mcandrews, Kevin  
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Bosco, Sam  
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Burr, David B.  
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Nakatsu, Cindy H.  
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Pellegrini, Gretel Gisela  
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McCabe, Linda D.  
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McCabe, George P.  
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Ferruzzi, Mario G.  
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Lila, Mary Ann  
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Peackock, Munro  
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Weaver, Connie M.  
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Bellido, Teresita M.  
dc.date.available
2023-04-13T13:47:44Z  
dc.date.issued
2019  
dc.identifier.citation
A blueberry-enriched diet counteracts the effects of estrogen deficiency in mice on bone, skeletal muscle, and peripheral fat, and alters the gut microbiome.; Annual Meeting Annual Meeting of the American Society for Bone and Mineral Research Orange County Convention Center; Estados Unidos; 2019; 1-6  
dc.identifier.uri
http://hdl.handle.net/11336/193693  
dc.description.abstract
Diets containing natural plant products exhibit protective effects on the adult skeleton by unclear mechanisms. We previously identified a blueberry cultivar (Montgomery= Mont) that protects from ovariectomy (OVX)-induced bone loss, when 10% lyophilized (freeze dried) berry was incorporated into a control diet (AIN-93M) and fed for 6 wks to sham/OVX 4 mo mice. We report here that bones from Mont-fed mice exhibited increased endogenous antioxidant response (EAR), assessed by phase-II detoxifying/antioxidant enzyme gene expression. In contrast, EAR was not increased in bones from mice fed 2 other berry-containing diets that did not protect from OVX-induced bone loss. Mont did not prevent OVX-induced reduction in the expression of C3, an estrogen receptor ERE-containing responsive gene. Thus, Mont diet specifically counteracted the harmful oxidative actions of OVX by increasing EAR, without activating canonical estrogenic actions in bone. Mont-fed mice were also protected from OVX-induced decreased BV/TV, TbTh, and TbN, assessed by micro-CT, and the increase in resorption (CTX). In addition, OVX induced skeletal muscle loss in control-fed mice, quantified by gastrocnemius weight, whereas Mont-fed mice were protected. Further, OVX control-fed mice exhibited increased body weight and peripheral fat mass, quantified by DEXA; and mice fed with Mont, but not with the 2 other berries, did not gain weight or peripheral fat upon OVX. We next examined potential effects of OVX and the Mont diet on the gut microbiome, known to affect homeostasis of several tissues. Fecal bacterial DNA was analyzed using 16S rRNA gene sequences from high throughput paired end MiSeq technology. We found that OVX did not induce significant changes in the microbiome regardless of the diet. In contrast, Mont-fed mice exhibited a statistically significant alteration of the microbiome compared with control- fed mice (axis1=54.4% per MANOVA, p=0.001). Further, analysis of the phylogenetic diversity detected higher prevalence of the bacterial communities Alloprevotella, Ruminococcus (starch fermenters), and an unclassified taxon Coriobacteriales Incertae in Mont-fed mice. In contrast, control-fed mice exhibited higher prevalence of Bifidobacterium and Coriobacteriaceae UCG-002 communities. These findings highlight the impact of nutrition on musculoskeletal tissue maintenance and the gut microbiome, and suggest alternative interventions to prevent the harmful effects of estrogen deficiency.  
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application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley Blackwell Publishing, Inc  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
blueberry diet  
dc.subject
estrogen deficiency  
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bone metabolism  
dc.subject
gut microbiome  
dc.subject.classification
Bioquímica y Biología Molecular  
dc.subject.classification
Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
A blueberry-enriched diet counteracts the effects of estrogen deficiency in mice on bone, skeletal muscle, and peripheral fat, and alters the gut microbiome.  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.type
info:eu-repo/semantics/conferenceObject  
dc.type
info:ar-repo/semantics/documento de conferencia  
dc.date.updated
2023-01-13T15:36:48Z  
dc.journal.pagination
1-6  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Washington  
dc.description.fil
Fil: Sato, Amy Y.. Indiana University; Estados Unidos  
dc.description.fil
Fil: Cregor, Meloney. Indiana University; Estados Unidos  
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Fil: Mcandrews, Kevin. Indiana University; Estados Unidos  
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Fil: Bosco, Sam. Indiana University; Estados Unidos  
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Fil: Burr, David B.. Indiana University; Estados Unidos  
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Fil: Nakatsu, Cindy H.. Purdue University; Estados Unidos  
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Fil: Pellegrini, Gretel Gisela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Inmunología, Genética y Metabolismo. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Inmunología, Genética y Metabolismo; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina  
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Fil: McCabe, Linda D.. Purdue University; Estados Unidos  
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Fil: McCabe, George P.. Purdue University; Estados Unidos  
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Fil: Ferruzzi, Mario G.. North Carolina State University; Estados Unidos  
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Fil: Lila, Mary Ann. North Carolina State University; Estados Unidos  
dc.description.fil
Fil: Peackock, Munro. Indiana University; Estados Unidos  
dc.description.fil
Fil: Weaver, Connie M.. Purdue University; Estados Unidos  
dc.description.fil
Fil: Bellido, Teresita M.. Indiana University; Estados Unidos  
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dc.coverage
Internacional  
dc.type.subtype
Reunión  
dc.description.nombreEvento
Annual Meeting Annual Meeting of the American Society for Bone and Mineral Research Orange County Convention Center  
dc.date.evento
2019-09-20  
dc.description.paisEvento
Estados Unidos  
dc.type.publicacion
Journal  
dc.description.institucionOrganizadora
American Society for Bone and Mineral Research  
dc.source.revista
Journal for Bone and Mineral Research  
dc.date.eventoHasta
2019-09-23  
dc.type
Reunión