Adıyaman Üniversitesi Kurumsal Arşivi

The effects of amlodipine and platelet rich plasma on bone healing in rats

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dc.contributor.author Atalay, Yusuf
dc.contributor.author Bozkurt, Mehmet Fatih
dc.contributor.author Gönül, Yücel
dc.contributor.author ve diğerleri...
dc.date.accessioned 2022-10-14T06:01:34Z
dc.date.available 2022-10-14T06:01:34Z
dc.date.issued 2015
dc.identifier.issn 1177-8881
dc.identifier.uri http://dspace.adiyaman.edu.tr:8080/xmlui/handle/20.500.12414/3730
dc.description.abstract Aim: The aim of this study was to evaluate the effects of calcium channel blocker (CCB) amlodipine (AML), platelet rich plasma (PRP), and a mixture of both materials on bone healing. Materials and methods: Fifty-six male Wistar rats were randomly divided into four groups: group A, tibia defect model with no treatment; group B, tibia defect model treated with AML, 0.04 mg daily by oral gavage; group C, tibia defect model treated with local PRP; group D, tibia defect model treated with local PRP and AML, 0.04 mg daily by oral gavage. Results: At day 21, bone healing was significantly better in groups C and D compared to group A (P<0.05), but comparisons showed no statistically significant difference in group B (P>0.05). At day 30, groups B and C showed no statistically significant difference (P>0.05) compared to group A, but bone healing in group D was significantly better than in group A (P<0.05). Statistically, AML did not affect alkaline phosphatase (ALP) activity at 21 and 30 days (P>0.05), but PRP and AML + PRP increased ALP activity statistically (P<0.05). Conclusion: It can be concluded that AML had neither a positive nor a negative effect on bone healing, but when used in combination with PRP, it may be beneficial. tr
dc.language.iso en tr
dc.publisher Dove Medical Press Ltd tr
dc.subject amlodipine tr
dc.subject calcium channel blockers tr
dc.subject platelet-rich plasma tr
dc.subject bone mineral metabolism tr
dc.subject hypertension tr
dc.title The effects of amlodipine and platelet rich plasma on bone healing in rats tr
dc.type Article tr
dc.contributor.authorID 0000-0002-1669-0988 tr
dc.contributor.department Afyon Kocatepe Univ, Fac Dent, Dept Oral & Maxillofacial Surg, TR-03030 Afyon, Turkey tr
dc.contributor.department Afyon Kocatepe Univ, Fac Vet Med, Dept Pathol, TR-03030 Afyon, Turkey tr
dc.identifier.endpage 1981 tr
dc.identifier.startpage 1973 tr
dc.identifier.volume 9 tr
dc.source.title Drug Design Development And Therapy tr


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