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The effect of an inhibitor of gut serotonin (LP533401) during the induction of periodontal disease

dc.contributor.authorLima, G M G
dc.contributor.authorCorazza, B J M
dc.contributor.authorMoraes, R. M.
dc.contributor.authorde Oliveira, F. E.
dc.contributor.authorde Oliveira, L. D.
dc.contributor.authorFranco, G C N
dc.contributor.authorPerrien, D. S.
dc.contributor.authorElefteriou, F.
dc.contributor.authorAnbinder, A. L.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Ponta Grossa (UEPG)
dc.date.accessioned2018-12-11T17:23:35Z
dc.date.available2018-12-11T17:23:35Z
dc.date.issued2016-10-01
dc.description.abstractBACKGROUND AND OBJECTIVE: LP533401 is an inhibitor of tryptophan hydroxylase 1, which regulates serotonin production in the gut. Previous work indicates that LP533401 has an anabolic effect in bone. Thus, we hypothesized that inhibition of gut serotonin production may modulate the host response in periodontal disease. In this study, we aimed to analyze the effects of LP533401 in a rat periodontitis model to evaluate the role of gut serotonin in periodontitis pathophysiology. MATERIAL AND METHODS: Twenty-four rats were divided into three groups: treated group (T: ligature-induced periodontal disease and LP533401, 25�mg/kg/d) by gavage; ligature group (L: ligature-induced periodontal disease only); and control group (C: without ligature-induced periodontal disease). After 28�d, radiographic alveolar bone support was measured on digital radiographs, and alveolar bone volume fraction, tissue mineral density and trabeculae characteristics were quantified by microcomputed tomography in the right hemi-mandible. Left hemi-mandibles were decalcified and alveolar bone loss, attachment loss and area of collagen in the gingiva were histologically analyzed. RESULTS: Significant difference between the L and C groups was found, confirming that periodontal disease was induced. We observed no difference between the T and L groups regarding alveolar bone destruction and area of collagen. CONCLUSION: LP533401 (25�mg/kg/d) for 28�d does not prevent bone loss and does not modulate host response in a rat model of induced periodontal disease.en
dc.description.affiliationDepartment of Bioscience and Oral Diagnosis, Institute of Science and Technology of S�o Jos� dos Campos, Univ Estadual Paulista - UNESP, S�o Jos� dos Campos, SP, Brazil
dc.description.affiliationDepartment of General Biology, State University of Ponta Grossa - UEPG, Ponta Grossa, Paran�, Brazil
dc.description.affiliationVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, USA
dc.description.affiliationDepartment of Orthopedic Surgery & Rehabilitation and Vanderbilt University Institute of Imaging Sciences, Vanderbilt University Medical Center, Nashville, TN, USA
dc.description.affiliationDepartment of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, TN, USA
dc.description.affiliationDepartments of Medicine, Pharmacology and Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, USA
dc.description.sponsorshipU.S. Department of Veterans Affairs
dc.description.sponsorshipNational Center for Research Resources
dc.description.sponsorshipIdU.S. Department of Veterans Affairs: IK2 BX001634
dc.description.sponsorshipIdNational Center for Research Resources: S10 RR027631
dc.format.extent661-668
dc.identifierhttp://dx.doi.org/10.1111/jre.12346
dc.identifier.citationJournal of periodontal research, v. 51, n. 5, p. 661-668, 2016.
dc.identifier.doi10.1111/jre.12346
dc.identifier.issn1600-0765
dc.identifier.scopus2-s2.0-85028259656
dc.identifier.urihttp://hdl.handle.net/11449/177038
dc.language.isoeng
dc.relation.ispartofJournal of periodontal research
dc.relation.ispartofsjr0,927
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectbone
dc.subjectenterochromaffin cells
dc.subjectperiodontitis
dc.subjectserotonin
dc.titleThe effect of an inhibitor of gut serotonin (LP533401) during the induction of periodontal diseaseen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes6097967943008273[9]
unesp.author.orcid0000-0003-3930-4274[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, São José dos Campospt
unesp.departmentBiociências e Diagnóstico Bucal - ICTpt

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