File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Simvastatin prevents alveolar bone loss in an experimental rat model of periodontitis after ovariectomy

TitleSimvastatin prevents alveolar bone loss in an experimental rat model of periodontitis after ovariectomy
Authors
KeywordsOsteoporosis
Alveolar bone loss
Maxillary
Periodontitis
Simvastatin
Issue Date2014
Citation
Journal of Translational Medicine, 2014, v. 12, n. 1, article no. 284 How to Cite?
Abstract© 2014 Xu et al.; licensee BioMed Central Ltd. Background: Periodontitis is an inflammatory disease characterized by the loss of connective tissue and alveolar bone. There is an increasing evidence that periodontitis is associated with a number of chronic disease, including osteoporosis. Periodontitis and osteoporosis are both bone destructive diseases and of high prevalence in adult population. Osteoporosis could increase some inflammatory factors that also participate in the progression of periodontitis, so as to facilitate the alveolar bone resorption. Simvastatin, specific inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme reductase, is of pleiotropic effects including anti-catabolic and anabolic effect on bone metabolism. This study aimed to explore the local and systemic effect of simvastatin on maxillary in rats with both osteoporosis and periodontitis.Methods: Thirty-six 4-month-old female Sprague Dawley rats were randomly assigned to six groups: sham group, ligature group, ovariectomized (OVX) + ligature group, local simvastatin administration to OVX + ligature rats (local simvastatin group), oral simvastatin administration to OVX + ligature rats (oral simvastatin group), local and oral simvastatin administration to OVX + ligature rats (L&O simvastatin group). One month after OVX, ligatures were placed on the maxillary first (M1) and second molars (M2) for 4 weeks on all rats except those in the sham group, followed by simvastatin treatment for 2 months. The maxillae, serum, and femurs were collected for further examination including micro-computed (micro-CT) tomography, hematoxylin and eosin (H&E) staining, tartrate-resistant acid phosphatase (TRAP) staining, enzyme-linked immunosorbent assays (ELISA), and the three-point bending test.Results: Local simvastatin administration increased alveolar crest height and prevented local alveolar bone loss without alteration of systemic bone loss. Oral administration prevented local and systemic bone loss with no effect on alveolar crest height.Conclusions: Our results indicate that simvastatin has the potential of promoting bone formation and reducing alveolar bone loss in maxillary following ovariectomy (OVX) and ligature placement in rats.
Persistent Identifierhttp://hdl.handle.net/10722/297335
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorXu, Xin-chen-
dc.contributor.authorChen, Hui-
dc.contributor.authorZhang, Xi-
dc.contributor.authorZhai, Zan-jing-
dc.contributor.authorLiu, Xu-qiang-
dc.contributor.authorQin, An-
dc.contributor.authorLu, Er-yi-
dc.date.accessioned2021-03-15T07:33:33Z-
dc.date.available2021-03-15T07:33:33Z-
dc.date.issued2014-
dc.identifier.citationJournal of Translational Medicine, 2014, v. 12, n. 1, article no. 284-
dc.identifier.urihttp://hdl.handle.net/10722/297335-
dc.description.abstract© 2014 Xu et al.; licensee BioMed Central Ltd. Background: Periodontitis is an inflammatory disease characterized by the loss of connective tissue and alveolar bone. There is an increasing evidence that periodontitis is associated with a number of chronic disease, including osteoporosis. Periodontitis and osteoporosis are both bone destructive diseases and of high prevalence in adult population. Osteoporosis could increase some inflammatory factors that also participate in the progression of periodontitis, so as to facilitate the alveolar bone resorption. Simvastatin, specific inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme reductase, is of pleiotropic effects including anti-catabolic and anabolic effect on bone metabolism. This study aimed to explore the local and systemic effect of simvastatin on maxillary in rats with both osteoporosis and periodontitis.Methods: Thirty-six 4-month-old female Sprague Dawley rats were randomly assigned to six groups: sham group, ligature group, ovariectomized (OVX) + ligature group, local simvastatin administration to OVX + ligature rats (local simvastatin group), oral simvastatin administration to OVX + ligature rats (oral simvastatin group), local and oral simvastatin administration to OVX + ligature rats (L&O simvastatin group). One month after OVX, ligatures were placed on the maxillary first (M1) and second molars (M2) for 4 weeks on all rats except those in the sham group, followed by simvastatin treatment for 2 months. The maxillae, serum, and femurs were collected for further examination including micro-computed (micro-CT) tomography, hematoxylin and eosin (H&E) staining, tartrate-resistant acid phosphatase (TRAP) staining, enzyme-linked immunosorbent assays (ELISA), and the three-point bending test.Results: Local simvastatin administration increased alveolar crest height and prevented local alveolar bone loss without alteration of systemic bone loss. Oral administration prevented local and systemic bone loss with no effect on alveolar crest height.Conclusions: Our results indicate that simvastatin has the potential of promoting bone formation and reducing alveolar bone loss in maxillary following ovariectomy (OVX) and ligature placement in rats.-
dc.languageeng-
dc.relation.ispartofJournal of Translational Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectOsteoporosis-
dc.subjectAlveolar bone loss-
dc.subjectMaxillary-
dc.subjectPeriodontitis-
dc.subjectSimvastatin-
dc.titleSimvastatin prevents alveolar bone loss in an experimental rat model of periodontitis after ovariectomy-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s12967-014-0284-0-
dc.identifier.pmid25269614-
dc.identifier.pmcidPMC4192445-
dc.identifier.scopuseid_2-s2.0-84907922958-
dc.identifier.volume12-
dc.identifier.issue1-
dc.identifier.spagearticle no. 284-
dc.identifier.epagearticle no. 284-
dc.identifier.eissn1479-5876-
dc.identifier.isiWOS:000345171600001-
dc.identifier.issnl1479-5876-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats