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The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats)
OBJECTIVES: Despite advances in maxillofacial surgery, impaired bone healing remains a concern for surgical teams. Many studies have evaluated the effects of sildenafil and pentoxifylline on bone healing. However, their effects on healing of bone fractures have not been well investigated. This study...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Oral and Maxillofacial Surgeons
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469969/ https://www.ncbi.nlm.nih.gov/pubmed/32855373 http://dx.doi.org/10.5125/jkaoms.2020.46.4.258 |
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author | MalekiGorji, Mohsen Golestaneh, Arash Razavi, Seyyed Mohammad |
author_facet | MalekiGorji, Mohsen Golestaneh, Arash Razavi, Seyyed Mohammad |
author_sort | MalekiGorji, Mohsen |
collection | PubMed |
description | OBJECTIVES: Despite advances in maxillofacial surgery, impaired bone healing remains a concern for surgical teams. Many studies have evaluated the effects of sildenafil and pentoxifylline on bone healing. However, their effects on healing of bone fractures have not been well investigated. This study aimed to assess the effects of the phosphodiesterase inhibitors sildenafil and pentoxifylline on healing of mandibular fractures in rats. MATERIALS AND METHODS: A total of 60 rats were randomly divided into six groups of 10. Mandibular fracture was induced in all rats. After the surgical procedure, group C1 received saline, group S1 received 10 mg/kg sildenafil and group P1 received 50 mg/kg pentoxifylline. The rats were sacrificed after 1 week. Groups C4, S4, and P4 received pharmaceutical therapy as in groups C1, S1, and P1 but were sacrificed after 4 weeks. The samples then underwent histological analysis. RESULTS: The mean rate of bone healing of mandibular fractures in groups S1 and P1 was significantly higher than in group C1 at 1 week (P<0.001). The mean rate of bone healing of mandibular fractures in group P1 was higher than in group S1 at 1 week (P=0.04). The mean rate of bone healing of mandibular fractures in groups S4 (P=0.001) and P4 (P=0.004) was significantly higher than in group C4 at 4 weeks, but no significant difference was noted in the rate of healing between groups P4 and S4 (P=0.53). CONCLUSION: Sildenafil and pentoxifylline can be used as adjuncts to enhance bone healing in rats. |
format | Online Article Text |
id | pubmed-7469969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Association of Oral and Maxillofacial Surgeons |
record_format | MEDLINE/PubMed |
spelling | pubmed-74699692020-09-11 The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) MalekiGorji, Mohsen Golestaneh, Arash Razavi, Seyyed Mohammad J Korean Assoc Oral Maxillofac Surg Original Article OBJECTIVES: Despite advances in maxillofacial surgery, impaired bone healing remains a concern for surgical teams. Many studies have evaluated the effects of sildenafil and pentoxifylline on bone healing. However, their effects on healing of bone fractures have not been well investigated. This study aimed to assess the effects of the phosphodiesterase inhibitors sildenafil and pentoxifylline on healing of mandibular fractures in rats. MATERIALS AND METHODS: A total of 60 rats were randomly divided into six groups of 10. Mandibular fracture was induced in all rats. After the surgical procedure, group C1 received saline, group S1 received 10 mg/kg sildenafil and group P1 received 50 mg/kg pentoxifylline. The rats were sacrificed after 1 week. Groups C4, S4, and P4 received pharmaceutical therapy as in groups C1, S1, and P1 but were sacrificed after 4 weeks. The samples then underwent histological analysis. RESULTS: The mean rate of bone healing of mandibular fractures in groups S1 and P1 was significantly higher than in group C1 at 1 week (P<0.001). The mean rate of bone healing of mandibular fractures in group P1 was higher than in group S1 at 1 week (P=0.04). The mean rate of bone healing of mandibular fractures in groups S4 (P=0.001) and P4 (P=0.004) was significantly higher than in group C4 at 4 weeks, but no significant difference was noted in the rate of healing between groups P4 and S4 (P=0.53). CONCLUSION: Sildenafil and pentoxifylline can be used as adjuncts to enhance bone healing in rats. The Korean Association of Oral and Maxillofacial Surgeons 2020-08-31 2020-08-31 /pmc/articles/PMC7469969/ /pubmed/32855373 http://dx.doi.org/10.5125/jkaoms.2020.46.4.258 Text en Copyright: © 2020 The Korean Association of Oral and Maxillofacial Surgeons. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article MalekiGorji, Mohsen Golestaneh, Arash Razavi, Seyyed Mohammad The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
title | The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
title_full | The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
title_fullStr | The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
title_full_unstemmed | The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
title_short | The effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
title_sort | effect of two phosphodiesterase inhibitors on bone healing in mandibular fractures (animal study in rats) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469969/ https://www.ncbi.nlm.nih.gov/pubmed/32855373 http://dx.doi.org/10.5125/jkaoms.2020.46.4.258 |
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