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The biochemical and histological analysis of subcutaneous calcitonin and intramedullary methylprednisolone on bone repair after bone marrow ablation: An experimental comparative study in rats

dc.contributor.authorErsözlü, S.
dc.contributor.authorSarısözen, B.
dc.contributor.authorÖzer, O.
dc.contributor.authorAdim, S.
dc.contributor.authorSahin, O.
dc.contributor.buuauthorBALABAN ADIM, ŞADUMAN
dc.contributor.buuauthorSARISÖZEN, MEHMET BARTU
dc.contributor.buuauthorÖzer, Özgür
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentOrtopedi ve Travmatoloji Ana Bilim Dalı
dc.contributor.scopusid55890736200
dc.contributor.scopusid8230556100
dc.contributor.scopusid15730076300
dc.date.accessioned2025-05-13T09:51:06Z
dc.date.issued2017-12-01
dc.description.abstractBackground: Although, glucocorticoid (GC) and calcitonin-induced changes in bone repair have been studied previously, the exact effects of these on fracture healing remain controversial. Hence, the purpose of this experimental study is to determine biochemical and histological effects of locally administrated GC and systemically administrated calcitonin on the kinetics of healing response after bone marrow ablation in rats. Methods: After having undergone marrow ablation, a steroid-treated group of rats (n = 24) received a single dose of intramedullary methylprednisolone (2 mg/kg), a calcitonin-treated group (n = 24) received intermittently administrated subcutaneous salmon calcitonin (16 IU/kg), and a control group (n = 24) received intramedullary saline (25 μl). Results: Blood samples taken on days 1, 3, 7, 9, and 15 after ablation showed an increase in serum calcium, alkaline phosphatase (ALP), and phosphate levels in the Calcitonin and Control groups. Levels of calcium and ALP peaked on day 7 after ablation. However, an increase in phosphate levels indicated a biphasic reaction that peaked on the third and ninth day after ablation. Hypercalcemia was not observed in Steroid group because of the inhibition of osteoclastic bone resorption. In that group, the serum levels of ALP and phosphate were lower than baseline levels. The levels of urinary calcium excretion peaked 3 to 7 days after marrow ablation in the control group and 7 to 9 days after that procedure in the steroid group. Histologic evaluation showed that the rats in the control group demonstrated the expected healing period according to the histological grades and that a delay in healing occurred in the calcitonin group after day 9 because of the inhibition of osteoclastic bone resorption. All rats in the steroid group exhibited a decrease and delayed healing response. Conclusion: Total serum calcium, phosphate, and ALP levels increased after bilateral tibial bone marrow ablation and urine calcium and hydroxyproline excretion also increased as a factor of bone resorption. Subcutaneously administrated salmon calcitonin did not affect biochemical changes after marrow ablation. Single-dose intramedullary methylprednisolone inhibited extra-tibial bone resorption induced by cytokines after bone marrow ablation.
dc.identifier.doi10.1186/s40634-017-0100-x
dc.identifier.issn2197-1153
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85066421204
dc.identifier.urihttps://hdl.handle.net/11452/52298
dc.identifier.volume4
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherSpringer Berlin Heidelberg
dc.relation.journalJournal of Experimental Orthopaedics
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMethylprednisolone
dc.subjectMarrow ablation
dc.subjectFracture healing
dc.subjectCalcitonin
dc.subjectBone repair
dc.subject.scopusCalcitonin's Role in Postmenopausal Osteoporosis Management
dc.titleThe biochemical and histological analysis of subcutaneous calcitonin and intramedullary methylprednisolone on bone repair after bone marrow ablation: An experimental comparative study in rats
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/ Ortopedi ve Travmatoloji Ana Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublication80df1863-762d-4cc1-9313-2d77d9e79ff8
relation.isAuthorOfPublicationda5292e3-7761-4cf8-a4e0-8f9099cf6469
relation.isAuthorOfPublication.latestForDiscovery80df1863-762d-4cc1-9313-2d77d9e79ff8

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