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dc.contributor.authorUsategui Martín, Ricardo 
dc.contributor.authorReal, Álvaro del
dc.contributor.authorSainz-Aja Guerra, José A.
dc.contributor.authorPrieto Lloret, Jesús 
dc.contributor.authorOlea Fraile, Elena 
dc.contributor.authorRocher Martín, María Asunción 
dc.contributor.authorRigual Bonastre, Ricardo Jaime 
dc.contributor.authorRiancho Moral, José Antonio
dc.contributor.authorPérez Castrillon, José Luis 
dc.date.accessioned2023-09-18T11:54:52Z
dc.date.available2023-09-18T11:54:52Z
dc.date.issued2022
dc.identifier.citationInternational Journal of Molecular Sciences, 2022, Vol. 23, Nº. 21, 12742es
dc.identifier.issn1422-0067es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/61612
dc.descriptionProducción Científicaes
dc.description.abstractHypoxia may be associated with alterations in bone remodeling, but the published results are contradictory. The aim of this study was to characterize the bone morphometry changes subject to hypoxia for a better understanding of the bone response to hypoxia and its possible clinical consequences on the bone metabolism. This study analyzed the bone morphometry parameters by micro-computed tomography (μCT) in rat and guinea pig normobaric hypoxia models. Adult male and female Wistar rats were exposed to chronic hypoxia for 7 and 15 days. Additionally, adult male guinea pigs were exposed to chronic hypoxia for 15 days. The results showed that rats exposed to chronic constant and intermittent hypoxic conditions had a worse trabecular and cortical bone health than control rats (under a normoxic condition). Rats under chronic constant hypoxia were associated with a more deteriorated cortical tibia thickness, trabecular femur and tibia bone volume over the total volume (BV/TV), tibia trabecular number (Tb.N), and trabecular femur and tibia bone mineral density (BMD). In the case of chronic intermittent hypoxia, rats subjected to intermittent hypoxia had a lower cortical femur tissue mineral density (TMD), lower trabecular tibia BV/TV, and lower trabecular thickness (Tb.Th) of the tibia and lower tibia Tb.N. The results also showed that obese rats under a hypoxic condition had worse values for the femur and tibia BV/TV, tibia trabecular separation (Tb.Sp), femur and tibia Tb.N, and BMD for the femur and tibia than normoweight rats under a hypoxic condition. In conclusion, hypoxia and obesity may modify bone remodeling, and thus bone microarchitecture, and they might lead to reductions in the bone strength and therefore increase the risk of fragility fracture.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherMDPIes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHypoxiaes
dc.subjectHipoxiaes
dc.subjectBiometryes
dc.subjectBiometríaes
dc.subjectBone remodelinges
dc.subjectHuesos - Regeneraciónes
dc.subjectBone - Diseaseses
dc.subjectHuesos - Enfermedades - Diagnósticoes
dc.subjectObesityes
dc.subjectObesidades
dc.subjectTomographyes
dc.subjectTomografía computadaes
dc.subjectAnimal Modelses
dc.subjectModelos animaleses
dc.subjectLaboratory animalses
dc.subjectAnimales de laboratorioes
dc.subjectAnimal experimentationes
dc.subjectExperimentación animales
dc.titleAnalysis of bone histomorphometry in rat and guinea pig animal models subject to hypoxiaes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2022 The Authorses
dc.identifier.doi10.3390/ijms232112742es
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/23/21/12742es
dc.identifier.publicationfirstpage12742es
dc.identifier.publicationissue21es
dc.identifier.publicationtitleInternational Journal of Molecular Scienceses
dc.identifier.publicationvolume23es
dc.peerreviewedSIes
dc.description.projectMinisterio de Economía y Competitividad y Fondo Europeo de Desarrollo Regional (FEDER) - (project BFU2015-70616-R)es
dc.description.projectJunta de Castilla y León, Consejería de Educación - (Grant CCVC8485)es
dc.identifier.essn1422-0067es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco2415 Biología Moleculares
dc.subject.unesco3201.04 Patología Clínicaes


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