Cyclosporine A impairs bone repair in critical defects filled with different osteoconductive bone substitutes.


Journal

Brazilian oral research
ISSN: 1807-3107
Titre abrégé: Braz Oral Res
Pays: Brazil
ID NLM: 101307187

Informations de publication

Date de publication:
2020
Historique:
received: 03 04 2019
accepted: 01 11 2019
entrez: 13 2 2020
pubmed: 13 2 2020
medline: 26 2 2020
Statut: epublish

Résumé

The aim of this study was to assess the influence of cyclosporine administration on the repair of critical-sized calvaria defects (CSDs) in rat calvaria filled with diverse biomaterials. Sixty animals were divided into two groups: the control (CTR) group (saline solution) and the cyclosporine (CCP) group (cyclosporine, 10 mg/kg/day). These medications were administered daily by gavage, beginning 15 days before the surgical procedure and lasting until the day the animals were euthanized. A CSD (5 mm Ø) was made in the calvaria of each animal, which was allocated to one of 3 subgroups, according to the biomaterial used to fill the defect: coagulum (COA), deproteinized bovine bone (DBB), or biphasic calcium phosphate ceramics of hydroxyapatite and β-phosphate tricalcium (HA/TCP). Euthanasia of the animals was performed 15 and 60 days after the surgical procedure (n = 5 animals/period/subgroup). Bone repair (formation) assessment was performed through microtomography and histometry, while the analyses of the expression of the BMP2, Osteocalcin, and TGFβ1 proteins were performed using immunohistochemistry. The CSDs not filled with biomaterials demonstrated lower bone formation in the CCP group. At 15 days, less bone formation was observed in the CSDs filled with DBB, a smaller volume of mineralized tissue was observed in the CSDs filled with HA/TCP, and the expression levels of BMP2 and osteocalcin were lower in the CCP group compared to the CTR group. The use of cyclosporine impaired bone repair in CSD, and this effect can be partially explained by the suppression of BMP2 and osteocalcin expression.

Identifiants

pubmed: 32049108
pii: S1806-83242020000100205
doi: 10.1590/1807-3107bor-2020.vol34.0007
pii:
doi:

Substances chimiques

Bmp2 protein, mouse 0
Bone Morphogenetic Protein 2 0
Bone Substitutes 0
Calcineurin Inhibitors 0
Tgfb1 protein, rat 0
Transforming Growth Factor beta1 0
Osteocalcin 104982-03-8
Cyclosporine 83HN0GTJ6D

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e007

Auteurs

Fernanda Castanheira Gonçalves (FC)

Universidade Estadual de São Paulo - Unesp, School of Dentistry Araraquara, Department of Diagnosis and Surgery, Araraquara, SP, Brazil.

Guilherme José Pimentel Lopes de Oliveira (GJPL)

Universidade Federal de Uberlândia - UFU, Dental School, Department of Periodontology, Uberlândia, MG, Brazil.

Cassio Rocha Scardueli (CR)

Universidade Estadual de São Paulo - Unesp, School of Dentistry Araraquara, Department of Diagnosis and Surgery, Araraquara, SP, Brazil.

Rubens Spin-Neto (R)

Aarhus University, Department of Dentistry and Oral Health, Section of Oral Radiology, Aarhus, Denmark.

Andreas Stavropoulos (A)

Malmo University, Department of Community Dentistry and Periodontology, Malmö, Sweden.

Rosemary Adriana Chiérici Marcantonio (RAC)

Universidade Estadual de São Paulo - Unesp, School of Dentistry Araraquara, Department of Diagnosis and Surgery, Araraquara, SP, Brazil.

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Classifications MeSH