dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:28:19Z
dc.date.accessioned2022-10-05T18:43:13Z
dc.date.available2014-05-27T11:28:19Z
dc.date.available2022-10-05T18:43:13Z
dc.date.created2014-05-27T11:28:19Z
dc.date.issued2013-02-01
dc.identifierInternational Journal of Experimental Pathology, v. 94, n. 1, p. 65-73, 2013.
dc.identifier0959-9673
dc.identifier1365-2613
dc.identifierhttp://hdl.handle.net/11449/74497
dc.identifier10.1111/iep.12007
dc.identifierWOS:000313723100102
dc.identifier2-s2.0-84872477323
dc.identifier2640929291808415
dc.identifier2402682969776875
dc.identifier0000-0001-7015-7175
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3923453
dc.description.abstractOsteonecrosis of the jaw (ONJ) following the use of bisphosphonates has become of increased interest in the scientific community, due in particular to its as-yet-unsolved pathogenesis. An experimental model of ONJ was induced in normal male rats [alendronate (ALN); 1 mg/Kg/day; n = 10] and matched controls (saline solution; n = 10). After 60 days of drug treatment, all animals were subjected to extractions of the left first lower molars and were euthanized at 3 and 28 days postsurgery. The following analyses were performed: (i) descriptive and quantitative (scores) histological evaluation, (ii) stereometry of distal sockets and (iii) biochemical measurement of C-telopeptide cross-linked collagen type I (CTX) and bone-specific alkaline phosphatase (BALP). The results showed that 28 days postsurgery the animals treated with ALN had areas of exposed and necrotic bone, associated with significant infection, especially in the interalveolar septum area and crestal regions, compared with controls. The levels of CTX, BALP and bone volume, as well as the degrees of inflammation and vascularization, were significantly reduced in these animals. Therefore, analysis of the data presented suggests that ALN therapy is associated with the development of osteonecrosis in the jaws of rodents after tooth extraction. © 2012 International Journal of Experimental Pathology.
dc.languageeng
dc.relationInternational Journal of Experimental Pathology
dc.relation1.938
dc.relation0,712
dc.relation0,712
dc.rightsAcesso restrito
dc.sourceScopus
dc.subjectAlendronate
dc.subjectOsteonecrosis
dc.subjectTooth extraction
dc.subjectalendronic acid
dc.subjectalkaline phosphatase bone isoenzyme
dc.subjectcarboxy terminal telopeptide
dc.subjectsodium chloride
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectbone mass
dc.subjectcontrolled study
dc.subjectexperimental study
dc.subjecthistopathology
dc.subjectjaw osteonecrosis
dc.subjectmale
dc.subjectmolar tooth
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectrat
dc.subjectrodent
dc.subjecttooth extraction
dc.subjectvascularization
dc.subjectAlkaline Phosphatase
dc.subjectAnimals
dc.subjectBiological Markers
dc.subjectBisphosphonate-Associated Osteonecrosis of the Jaw
dc.subjectBone Remodeling
dc.subjectCollagen Type I
dc.subjectDisease Models, Animal
dc.subjectJaw
dc.subjectMale
dc.subjectMolar
dc.subjectPeptides
dc.subjectRats
dc.subjectTime Factors
dc.subjectTooth Extraction
dc.subjectWeight Gain
dc.titleExperimental development of bisphosphonate-related osteonecrosis of the jaws in rodents
dc.typeArtigo


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