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- Publisher Website: 10.1016/j.jcms.2006.02.005
- Scopus: eid_2-s2.0-33745240973
- PMID: 16777428
- WOS: WOS:000239374500004
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Article: Effect of recombinant human tissue inhibitor of matrix metalloproteinase-1 in rabbit mandibular distraction osteogenesis: a histological and immunohistochemical study
Title | Effect of recombinant human tissue inhibitor of matrix metalloproteinase-1 in rabbit mandibular distraction osteogenesis: a histological and immunohistochemical study |
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Authors | |
Keywords | Bone matrix metalloproteinase Distraction osteogenesis Immunohistochemistry Mandible Rabbit Tissue inhibitor of matrix metalloproteinase |
Issue Date | 2006 |
Publisher | Churchill Livingstone. The Journal's web site is located at http://www.elsevier.com/locate/jcms |
Citation | Journal of Cranio-Maxillofacial Surgery, 2006, v. 34 n. 5, p. 277-282 How to Cite? |
Abstract | Background: Bone matrix metalloproteinases are capable of degrading bone matrix during the remodelling, and their degradation activities can be down regulated by the tissue inhibitors of matrix metalloproteinases. This study evaluated the influence of exogenous tissue inhibitor of matrix metalloproteinase-1 on the expression of matrix metalloproteinases and endogenous tissue inhibitor of matrix metalloproteinases in mandibular distraction osteogenesis. Material and Methods: Fifteen New Zealand white rabbits were assigned to three groups: a negative control; a sham control group implanted with a collagen sheet; and an experimental group implanted with recombinant human tissue inhibitor of matrix metalloproteinase-1 impregnated in a collagen sheet. Rabbits were sacrificed at 6 weeks, 12 weeks and 24 weeks of consolidation. Results: Major expression of matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases was observed at the early stage of consolidation, only positive signals of tissue inhibitors of matrix metalloproteinases were observed at 24 weeks. The addition of recombinant human tissue inhibitor of matrix metalloproteinases-1 did not affect bone maturation and remodelling. Conclusions: An equilibrium of bone formation and resorption was reached at 24 weeks of consolidation in the rabbit mandible. No obvious influence of recombinant human tissue inhibitor of matrix metalloproteinase-1 on bone remodelling of mandibular distraction osteogenesis was noted. © 2006 European Association for Cranio-Maxillofacial Surgery. |
Persistent Identifier | http://hdl.handle.net/10722/90753 |
ISSN | 2023 Impact Factor: 2.1 2023 SCImago Journal Rankings: 1.031 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Zheng, L | en_HK |
dc.contributor.author | Ma, L | en_HK |
dc.contributor.author | Rabie, ABM | en_HK |
dc.contributor.author | Cheung, LK | en_HK |
dc.date.accessioned | 2010-09-17T10:07:47Z | - |
dc.date.available | 2010-09-17T10:07:47Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Journal of Cranio-Maxillofacial Surgery, 2006, v. 34 n. 5, p. 277-282 | en_HK |
dc.identifier.issn | 1010-5182 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/90753 | - |
dc.description.abstract | Background: Bone matrix metalloproteinases are capable of degrading bone matrix during the remodelling, and their degradation activities can be down regulated by the tissue inhibitors of matrix metalloproteinases. This study evaluated the influence of exogenous tissue inhibitor of matrix metalloproteinase-1 on the expression of matrix metalloproteinases and endogenous tissue inhibitor of matrix metalloproteinases in mandibular distraction osteogenesis. Material and Methods: Fifteen New Zealand white rabbits were assigned to three groups: a negative control; a sham control group implanted with a collagen sheet; and an experimental group implanted with recombinant human tissue inhibitor of matrix metalloproteinase-1 impregnated in a collagen sheet. Rabbits were sacrificed at 6 weeks, 12 weeks and 24 weeks of consolidation. Results: Major expression of matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases was observed at the early stage of consolidation, only positive signals of tissue inhibitors of matrix metalloproteinases were observed at 24 weeks. The addition of recombinant human tissue inhibitor of matrix metalloproteinases-1 did not affect bone maturation and remodelling. Conclusions: An equilibrium of bone formation and resorption was reached at 24 weeks of consolidation in the rabbit mandible. No obvious influence of recombinant human tissue inhibitor of matrix metalloproteinase-1 on bone remodelling of mandibular distraction osteogenesis was noted. © 2006 European Association for Cranio-Maxillofacial Surgery. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Churchill Livingstone. The Journal's web site is located at http://www.elsevier.com/locate/jcms | en_HK |
dc.relation.ispartof | Journal of Cranio-Maxillofacial Surgery | en_HK |
dc.subject | Bone matrix metalloproteinase | en_HK |
dc.subject | Distraction osteogenesis | en_HK |
dc.subject | Immunohistochemistry | en_HK |
dc.subject | Mandible | en_HK |
dc.subject | Rabbit | en_HK |
dc.subject | Tissue inhibitor of matrix metalloproteinase | en_HK |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Bone Remodeling - drug effects | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Mandible - drug effects - pathology - surgery | en_HK |
dc.subject.mesh | Matrix Metalloproteinase 1 - drug effects | en_HK |
dc.subject.mesh | Models, Animal | en_HK |
dc.subject.mesh | Osteogenesis, Distraction - methods | en_HK |
dc.subject.mesh | Protease Inhibitors - pharmacology | en_HK |
dc.subject.mesh | Rabbits | en_HK |
dc.subject.mesh | Tissue Inhibitor of Metalloproteinase-1 - pharmacology | en_HK |
dc.title | Effect of recombinant human tissue inhibitor of matrix metalloproteinase-1 in rabbit mandibular distraction osteogenesis: a histological and immunohistochemical study | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Zheng, L: lwzheng@hku.hk | en_HK |
dc.identifier.email | Rabie, ABM: rabie@hku.hk | en_HK |
dc.identifier.email | Cheung, L: lkcheung@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zheng, LW=rp01411 | en_HK |
dc.identifier.authority | Rabie, ABM=rp00029 | en_HK |
dc.identifier.authority | Cheung, L=rp00013 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jcms.2006.02.005 | en_HK |
dc.identifier.pmid | 16777428 | - |
dc.identifier.scopus | eid_2-s2.0-33745240973 | en_HK |
dc.identifier.hkuros | 123846 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33745240973&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 34 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 277 | en_HK |
dc.identifier.epage | 282 | en_HK |
dc.identifier.isi | WOS:000239374500004 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Zheng, LW=11241247300 | en_HK |
dc.identifier.scopusauthorid | Ma, L=36072648200 | en_HK |
dc.identifier.scopusauthorid | Rabie, ABM=7007172734 | en_HK |
dc.identifier.scopusauthorid | Cheung, LK=7102302747 | en_HK |
dc.identifier.issnl | 1010-5182 | - |