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The impact of Resolvin E1 on bone regeneration in critical‐sized calvarial defects of rat model—A gene expression and micro‐CT analysis
Objective To investigate, in vivo, the effect of local application of Resolvin E1 (RvE1) on the bone regeneration of critical‐size defects (CSDs) in Wistar rats utilizing gene expression and micro‐computed tomographic (micro‐CT) analysis. Background The inflammation‐resolving actions of RvE1 are wel...
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Published in: | Journal of periodontal research 2024-02, Vol.59 (1), p.195-203 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Objective
To investigate, in vivo, the effect of local application of Resolvin E1 (RvE1) on the bone regeneration of critical‐size defects (CSDs) in Wistar rats utilizing gene expression and micro‐computed tomographic (micro‐CT) analysis.
Background
The inflammation‐resolving actions of RvE1 are well established. The molecular mechanism of its bone‐regenerative actions has been of significant interest in recent years; however, there is limited information regarding the same.
Materials and Methods
Thirty Wistar rats with a 5 mm induced critical‐size calvarial defect were randomly allocated into four groups: no treatment/negative control (n = 5), treatment using bovine bone grafts/positive control (n = 5), treatment using local delivery of RvE1 (n = 11) and treatment using RvE1 mixed with bovine bone graft (n = 9). After 4 weeks, RNA isolation, complementary DNA synthesis and real‐time polymerase chain reaction were used for genetic expression of alkaline phosphatase (ALP), osteocalcin (OCN) and osteopontin (OPN). The rats were sacrificed after 12 weeks and micro‐CT imaging was performed to analyse the characteristics of the newly formed bone (NFB). The data were analysed using ANOVA and the least significant difference tests (α ≤ .05).
Results
The RvE1 + bovine graft group had statistically highest mean NFB (20.75 ± 2.67 mm3) compared to other groups (p |
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ISSN: | 0022-3484 1600-0765 |
DOI: | 10.1111/jre.13206 |