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Evaluation of Bone–Implant Interface: Effects of Angiotensin II Receptor Blockade in Hypertensive Rats

dc.contributor.authorMulinari-Santos, Gabriel [UNESP]
dc.contributor.authorSantos, Jaqueline Silva dos [UNESP]
dc.contributor.authorde Souza Batista, Fábio Roberto [UNESP]
dc.contributor.authorPitol-Palin, Letícia [UNESP]
dc.contributor.authorSilva, Ana Cláudia Ervolino da [UNESP]
dc.contributor.authorBotacin, Paulo Roberto [UNESP]
dc.contributor.authorAntoniali, Cristina [UNESP]
dc.contributor.authorOkamoto, Roberta [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:38:06Z
dc.date.issued2025-01-01
dc.description.abstractHypertension is a global health concern not only correlated with cardiovascular complications, but also with impaired bone metabolism, potentially affecting healing at the bone–implant interface. Losartan, an angiotensin II receptor blocker (ARB) commonly prescribed for hypertension, has shown beneficial effects on bone healing in spontaneously hypertensive rats (SHRs). However, the influence of hypertension and ARBs like losartan on the bone cellular response at the bone–implant interface remains underexplored. Methods: A total of 32 rats were included in this study: 16 SHRs, with 8 receiving losartan (30 mg/kg daily) and 8 receiving no treatment, and 16 normotensive Wistar rats, with 8 receiving losartan and 8 receiving no treatment. After one week of treatment, titanium implants were placed into the tibia of all the animals. The bone–implant interface was assessed 60 days post-implantation using micro-computed tomography (µCT) and an immunohistochemical analysis. Results: (i) The ARB treatment significantly increased the bone volume and bone–implant contact in the SHRs receiving losartan compared to the untreated SHRs. (ii) Consistent with the µCT findings, the immunohistochemistry further confirmed regular bone turnover and increased osteocalcin (OC) mineralization in the treated SHRs. In contrast, no alterations in the bone microarchitecture were noted in the Wistar rats treated with losartan. Conclusions: The results suggest that losartan, an ARB drug, improves bone volume and bone turnover at the bone–implant interface in SHRs.en
dc.description.affiliationDepartment of Basic Sciences Araçatuba School of Dentistry São Paulo State University, SP
dc.description.affiliationDepartment of Diagnosis and Surgery Araçatuba School of Dentistry São Paulo State University, SP
dc.description.affiliationUnespDepartment of Basic Sciences Araçatuba School of Dentistry São Paulo State University, SP
dc.description.affiliationUnespDepartment of Diagnosis and Surgery Araçatuba School of Dentistry São Paulo State University, SP
dc.identifierhttp://dx.doi.org/10.3390/coatings15010073
dc.identifier.citationCoatings, v. 15, n. 1, 2025.
dc.identifier.doi10.3390/coatings15010073
dc.identifier.issn2079-6412
dc.identifier.scopus2-s2.0-85216004222
dc.identifier.urihttps://hdl.handle.net/11449/298758
dc.language.isoeng
dc.relation.ispartofCoatings
dc.sourceScopus
dc.subjectimplants
dc.subjectlosartan
dc.subjectosseointegration
dc.subjectspontaneously hypertensive rats
dc.titleEvaluation of Bone–Implant Interface: Effects of Angiotensin II Receptor Blockade in Hypertensive Ratsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.orcid0000-0002-8651-9270[2]
unesp.author.orcid0000-0003-4765-3765[4]
unesp.author.orcid0000-0002-0315-6161[7]
unesp.author.orcid0000-0002-6773-6966[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt

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